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73 jobs found in massachusetts

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    • waltham, massachusetts
    • contract
    • $38 - $42.90 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Waltham, Massachusetts job type: Contract salary: $38.00 - 42.90 per hour work hours: 9 to 5 education: Bachelors   responsibilities: - Provides direct on-site early formulation development support to enable efficacy, PK, and toxicology studies for small molecule Drug Discovery efforts. - Provides drug substance characterization including crystallinity assessment, solubility determination, and physicochemical stability evaluation. - Offers solubility enhancement of poor water soluble compounds by applying various solubilization techniques. - Develops understanding of the impact of physiochemical and solid state properties on drug candidate performance. - Perform in-silico biopharmaceutical evaluation to support drugability assessment. - Inform and influence drug discovery team finding new chemical entities with desirable physicochemical and biopharmaceutical properties. - Recommends potential clinical formulation to the project team based on physicochemical and biopharmaceutical properties of the drug candidate.   qualifications: - Knowledge in discovery and preclinical formulation support, preformulation screening, solid state characterization and aiding formulation design. Analytical mindset on analyzing formulation, and hands-on experience on instruments such as HPLC, dissolution, microscope, and particle size analysis, - Self-motivated with capabilities in executing tasks independently, following protocols accurately, managing time efficiently, delivering formulations accurately and timely, and collaborating with other team members professionally. - Good written and verbal communication skills. - B.S./M.S./Ph.D. in pharmaceutics, pharmaceutical science, pharmaceutical chemistry or related scientific discipline required. - Prefer 1 to 2 years of relevant experience in discovery and preclinical support, preformulation screening, early formulation development, and solid state characterization in the pharmaceutical industry. Education - Minimum BS, prefer MS or PhD, in Pharmaceutics, pharmaceutical science, pharmaceutical chemistry or related scientific discipline required.   skills: HPLC, Chemistry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Waltham, Massachusetts job type: Contract salary: $38.00 - 42.90 per hour work hours: 9 to 5 education: Bachelors   responsibilities: - Provides direct on-site early formulation development support to enable efficacy, PK, and toxicology studies for small molecule Drug Discovery efforts. - Provides drug substance characterization including crystallinity assessment, solubility determination, and physicochemical stability evaluation. - Offers solubility enhancement of poor water soluble compounds by applying various solubilization techniques. - Develops understanding of the impact of physiochemical and solid state properties on drug candidate performance. - Perform in-silico biopharmaceutical evaluation to support drugability assessment. - Inform and influence drug discovery team finding new chemical entities with desirable physicochemical and biopharmaceutical properties. - Recommends potential clinical formulation to the project team based on physicochemical and biopharmaceutical properties of the drug candidate.   qualifications: - Knowledge in discovery and preclinical formulation support, preformulation screening, solid state characterization and aiding formulation design. Analytical mindset on analyzing formulation, and hands-on experience on instruments such as HPLC, dissolution, microscope, and particle size analysis, - Self-motivated with capabilities in executing tasks independently, following protocols accurately, managing time efficiently, delivering formulations accurately and timely, and collaborating with other team members professionally. - Good written and verbal communication skills. - B.S./M.S./Ph.D. in pharmaceutics, pharmaceutical science, pharmaceutical chemistry or related scientific discipline required. - Prefer 1 to 2 years of relevant experience in discovery and preclinical support, preformulation screening, early formulation development, and solid state characterization in the pharmaceutical industry. Education - Minimum BS, prefer MS or PhD, in Pharmaceutics, pharmaceutical science, pharmaceutical chemistry or related scientific discipline required.   skills: HPLC, Chemistry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • norwood, massachusetts
    • contract
    • $53.13 - $62.50 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Norwood, Massachusetts job type: Contract salary: $53.13 - 62.50 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Position Description: We are seeking a highly motivated candidate to join our Automation Engineer (Liquid Handler) team within a Top 10 BioPharma industry leader. This will be a hands-on, impactful position reporting to the Sr. Principal Automation Engineer. You will support scientist by improving existing processes and automating manual lab processes. You will work in a team environment with other Automation Engineers to design an implement liquid handler method. Additionally, you will be responsible to assure the operational functionality of the instruments as according to manufacturer's specifications. You will be a key individual for critical automation support for high-throughput screening, assay development, sample management, and lab automated solutions. This is a hybrid role - remote programming from home with on-site wet tests required. May need to travel to two site locations-Cambridge, MA and Norwood, MA Job Description Develop and optimize new liquid handler protocols for the screening and high-throughput assay platforms, specifically using Hamilton Venus.Assist scientists with operation of automation platforms.Provide error-recovery support as needed.Partner with business partners for requirements and issue tracking.Track/record problems with the systems for proper troubleshooting.Explore and evaluate modern technologies in automation, liquid handling, sample analysis, etc.Train users on new methods and protocols of system functionality Capabilities to automate analytical processes using Hamilton or other platformsEducate users about lab automation instruments and their capabilitiesCoordinate with internal and external groups to identify appropriate solutions to improve analytical testing capacity and efficiency  qualifications: Critical Skills Excellent verbal and written communication skillsExperience with HT liquid handling system operation, troubleshooting, and maintenanceWith training, have the ability to successfully automate manual lab processesInitiative, independence, and the ability to execute lab work under minimal supervisionThe successful candidate will have an analytical mindset, creative problem-solving skills, and be methodical and organizedAbility to communicate at various levels within the organization as well as with external vendorsAbility to troubleshoot and resolve issues that arise with liquid handling equipment. Basic Qualifications Requires a BS in biology/engineering/biotechnologyMinimum experience required of 2+ years in industry,?preferably in a setting with lab automation ?Preferred Qualifications Experience with Hamilton liquid handlers strongly preferred.Experience and skills in creating, modifying, and troubleshooting robotics/automation scripts.Familiarity with Atlassian tools for version control (Bitbucket) and issue management (Jira)Experience with Tecan, Hudson, High-Res, Echo desired Working Environment This is a hybrid role - remote programming from home with on-site wet tests requiredMay need to travel to two site locations-Cambridge, MA and Norwood, MAEmployee maybe required to manage hazardous wastes in compliance with company procedures & State/Federal/Local hazardous waste regulations. Duties may include Identifying, handling, generating, accumulating, storing, and labeling  skills: Biology Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Norwood, Massachusetts job type: Contract salary: $53.13 - 62.50 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Position Description: We are seeking a highly motivated candidate to join our Automation Engineer (Liquid Handler) team within a Top 10 BioPharma industry leader. This will be a hands-on, impactful position reporting to the Sr. Principal Automation Engineer. You will support scientist by improving existing processes and automating manual lab processes. You will work in a team environment with other Automation Engineers to design an implement liquid handler method. Additionally, you will be responsible to assure the operational functionality of the instruments as according to manufacturer's specifications. You will be a key individual for critical automation support for high-throughput screening, assay development, sample management, and lab automated solutions. This is a hybrid role - remote programming from home with on-site wet tests required. May need to travel to two site locations-Cambridge, MA and Norwood, MA Job Description Develop and optimize new liquid handler protocols for the screening and high-throughput assay platforms, specifically using Hamilton Venus.Assist scientists with operation of automation platforms.Provide error-recovery support as needed.Partner with business partners for requirements and issue tracking.Track/record problems with the systems for proper troubleshooting.Explore and evaluate modern technologies in automation, liquid handling, sample analysis, etc.Train users on new methods and protocols of system functionality Capabilities to automate analytical processes using Hamilton or other platformsEducate users about lab automation instruments and their capabilitiesCoordinate with internal and external groups to identify appropriate solutions to improve analytical testing capacity and efficiency  qualifications: Critical Skills Excellent verbal and written communication skillsExperience with HT liquid handling system operation, troubleshooting, and maintenanceWith training, have the ability to successfully automate manual lab processesInitiative, independence, and the ability to execute lab work under minimal supervisionThe successful candidate will have an analytical mindset, creative problem-solving skills, and be methodical and organizedAbility to communicate at various levels within the organization as well as with external vendorsAbility to troubleshoot and resolve issues that arise with liquid handling equipment. Basic Qualifications Requires a BS in biology/engineering/biotechnologyMinimum experience required of 2+ years in industry,?preferably in a setting with lab automation ?Preferred Qualifications Experience with Hamilton liquid handlers strongly preferred.Experience and skills in creating, modifying, and troubleshooting robotics/automation scripts.Familiarity with Atlassian tools for version control (Bitbucket) and issue management (Jira)Experience with Tecan, Hudson, High-Res, Echo desired Working Environment This is a hybrid role - remote programming from home with on-site wet tests requiredMay need to travel to two site locations-Cambridge, MA and Norwood, MAEmployee maybe required to manage hazardous wastes in compliance with company procedures & State/Federal/Local hazardous waste regulations. Duties may include Identifying, handling, generating, accumulating, storing, and labeling  skills: Biology Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts
    • contract
    • $53.13 - $62.50 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $53.13 - 62.50 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Position Description: We are seeking a highly motivated candidate to join our Automation Engineer (Liquid Handler) team within a Top 10 BioPharma industry leader. This will be a hands-on, impactful position reporting to the Sr. Principal Automation Engineer. You will support scientist by improving existing processes and automating manual lab processes. You will work in a team environment with other Automation Engineers to design an implement liquid handler method. Additionally, you will be responsible to assure the operational functionality of the instruments as according to manufacturer's specifications. You will be a key individual for critical automation support for high-throughput screening, assay development, sample management, and lab automated solutions. This is a hybrid role - remote programming from home with on-site wet tests required. May need to travel to two site locations-Cambridge, MA and Norwood, MA Job Description Develop and optimize new liquid handler protocols for the screening and high-throughput assay platforms, specifically using Hamilton Venus.Assist scientists with operation of automation platforms.Provide error-recovery support as needed.Partner with business partners for requirements and issue tracking.Track/record problems with the systems for proper troubleshooting.Explore and evaluate modern technologies in automation, liquid handling, sample analysis, etc.Train users on new methods and protocols of system functionality Capabilities to automate analytical processes using Hamilton or other platformsEducate users about lab automation instruments and their capabilitiesCoordinate with internal and external groups to identify appropriate solutions to improve analytical testing capacity and efficiency  qualifications: Critical Skills Excellent verbal and written communication skillsExperience with HT liquid handling system operation, troubleshooting, and maintenanceWith training, have the ability to successfully automate manual lab processesInitiative, independence, and the ability to execute lab work under minimal supervisionThe successful candidate will have an analytical mindset, creative problem-solving skills, and be methodical and organizedAbility to communicate at various levels within the organization as well as with external vendorsAbility to troubleshoot and resolve issues that arise with liquid handling equipment. Basic Qualifications Requires a BS in biology/engineering/biotechnologyMinimum experience required of 2+ years in industry,?preferably in a setting with lab automation ?Preferred Qualifications Experience with Hamilton liquid handlers strongly preferred.Experience and skills in creating, modifying, and troubleshooting robotics/automation scripts.Familiarity with Atlassian tools for version control (Bitbucket) and issue management (Jira)Experience with Tecan, Hudson, High-Res, Echo desired Working Environment This is a hybrid role - remote programming from home with on-site wet tests requiredMay need to travel to two site locations-Cambridge, MA and Norwood, MAEmployee maybe required to manage hazardous wastes in compliance with company procedures & State/Federal/Local hazardous waste regulations. Duties may include Identifying, handling, generating, accumulating, storing, and labeling  skills: Biology Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $53.13 - 62.50 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Position Description: We are seeking a highly motivated candidate to join our Automation Engineer (Liquid Handler) team within a Top 10 BioPharma industry leader. This will be a hands-on, impactful position reporting to the Sr. Principal Automation Engineer. You will support scientist by improving existing processes and automating manual lab processes. You will work in a team environment with other Automation Engineers to design an implement liquid handler method. Additionally, you will be responsible to assure the operational functionality of the instruments as according to manufacturer's specifications. You will be a key individual for critical automation support for high-throughput screening, assay development, sample management, and lab automated solutions. This is a hybrid role - remote programming from home with on-site wet tests required. May need to travel to two site locations-Cambridge, MA and Norwood, MA Job Description Develop and optimize new liquid handler protocols for the screening and high-throughput assay platforms, specifically using Hamilton Venus.Assist scientists with operation of automation platforms.Provide error-recovery support as needed.Partner with business partners for requirements and issue tracking.Track/record problems with the systems for proper troubleshooting.Explore and evaluate modern technologies in automation, liquid handling, sample analysis, etc.Train users on new methods and protocols of system functionality Capabilities to automate analytical processes using Hamilton or other platformsEducate users about lab automation instruments and their capabilitiesCoordinate with internal and external groups to identify appropriate solutions to improve analytical testing capacity and efficiency  qualifications: Critical Skills Excellent verbal and written communication skillsExperience with HT liquid handling system operation, troubleshooting, and maintenanceWith training, have the ability to successfully automate manual lab processesInitiative, independence, and the ability to execute lab work under minimal supervisionThe successful candidate will have an analytical mindset, creative problem-solving skills, and be methodical and organizedAbility to communicate at various levels within the organization as well as with external vendorsAbility to troubleshoot and resolve issues that arise with liquid handling equipment. Basic Qualifications Requires a BS in biology/engineering/biotechnologyMinimum experience required of 2+ years in industry,?preferably in a setting with lab automation ?Preferred Qualifications Experience with Hamilton liquid handlers strongly preferred.Experience and skills in creating, modifying, and troubleshooting robotics/automation scripts.Familiarity with Atlassian tools for version control (Bitbucket) and issue management (Jira)Experience with Tecan, Hudson, High-Res, Echo desired Working Environment This is a hybrid role - remote programming from home with on-site wet tests requiredMay need to travel to two site locations-Cambridge, MA and Norwood, MAEmployee maybe required to manage hazardous wastes in compliance with company procedures & State/Federal/Local hazardous waste regulations. Duties may include Identifying, handling, generating, accumulating, storing, and labeling  skills: Biology Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north billerica, massachusetts
    • permanent
    • $95,000 - $125,000 per year
    The objective of this position is to provide supervision of operations associated with pharmaceutical product manufacturing (non-radioactive) on the Billerica Campus, while ensuring that all operations comply with all GMP, OSHA and other regulatory requirements.  The Supervisor reports to the first Shift Manufacturing Manager and leads the execution of commercial pharmaceutical manufacturing according to standard operating procedures and production records in accordance with Current Good Manufacturing Practices (cGMP’s). The Supervisor is responsible for on-the-floor leadership of a team of manufacturing technicians whose primary focus is on execution of the manufacturing processes.  In addition to commercial production, the first shift Supervisor is responsible for compliance with internal and external guidance, technical assessment of the processes, innovation, and reliability. salary: $95,000 - $125,000 per yearshift: Secondwork hours: 4 PM - 2 AMeducation: BachelorResponsibilities Achieves the production schedule by coordinating materials, equipment, personnel, utilities and activities within his/her team, the second shift Supervisor and with partner organizations.  Ensures department goals and metrics are meeting or exceeding expectations.  Independently identifies deficiencies, creates and executes action plans to mitigate issues.  Build strong partnership with process support and facilities teams to ensure operations are supported by on-time maintenance and calibration.  Actively promotes a productive and cooperative environment by empowering resources to set and achieve goals together. SkillsManufacturing (2 years of experience is required)GMP (1 year of experience is required)Supervising (1 year of experience is required)Visual InspectionQualificationsYears of experience: 2 yearsExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    The objective of this position is to provide supervision of operations associated with pharmaceutical product manufacturing (non-radioactive) on the Billerica Campus, while ensuring that all operations comply with all GMP, OSHA and other regulatory requirements.  The Supervisor reports to the first Shift Manufacturing Manager and leads the execution of commercial pharmaceutical manufacturing according to standard operating procedures and production records in accordance with Current Good Manufacturing Practices (cGMP’s). The Supervisor is responsible for on-the-floor leadership of a team of manufacturing technicians whose primary focus is on execution of the manufacturing processes.  In addition to commercial production, the first shift Supervisor is responsible for compliance with internal and external guidance, technical assessment of the processes, innovation, and reliability. salary: $95,000 - $125,000 per yearshift: Secondwork hours: 4 PM - 2 AMeducation: BachelorResponsibilities Achieves the production schedule by coordinating materials, equipment, personnel, utilities and activities within his/her team, the second shift Supervisor and with partner organizations.  Ensures department goals and metrics are meeting or exceeding expectations.  Independently identifies deficiencies, creates and executes action plans to mitigate issues.  Build strong partnership with process support and facilities teams to ensure operations are supported by on-time maintenance and calibration.  Actively promotes a productive and cooperative environment by empowering resources to set and achieve goals together. SkillsManufacturing (2 years of experience is required)GMP (1 year of experience is required)Supervising (1 year of experience is required)Visual InspectionQualificationsYears of experience: 2 yearsExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north billerica, massachusetts
    • permanent
    • $55,000 - $62,000 per year
    2nd shift hours available for Manufacturing Tech 4 in Billerica, MA  The objective of this position is to perform manufacturing operations required to produce pharmaceutical products in a timely manner compliant with cGMP, OSHA, and other regulatory requirements. Under the direction and on-the-floor guidance of the 2nd Shift Manufacturing Supervisor, the Manufacturing Technician IV will become qualified and independently capable of performing all aspects of internal cold manufacturing operations.  Such operations include, but are not limited to, receipt and transfer of materials and components into the manufacturing unit operation, component and equipment cleaning and preparation, operation of automated manufacturing equipment with good aseptic technique, completion of production transactions within the ERP system, completion of paper-based production records and forms in accordance with GDP. 3 – 5 years of experience in a pharmaceutical/biotech manufacturing or quality environment.salary: $55,000 - $62,000 per yearshift: Secondwork hours: 4 PM - 2:30 AMeducation: High` SchoolResponsibilitiesThis individual will support qualification activities and routine operator maintenance for manufacturing equipment, and will assist with inventory management in designated manufacturing areas.SkillsManufacturing (3 years of experience is required)GMP (1 year of experience is required)aseptic techniques (1 year of experience is preferred)Standard Operating Procedures (1 year of experience is preferred)Batch Records (1 year of experience is preferred)QualificationsYears of experience: 1 yearExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    2nd shift hours available for Manufacturing Tech 4 in Billerica, MA  The objective of this position is to perform manufacturing operations required to produce pharmaceutical products in a timely manner compliant with cGMP, OSHA, and other regulatory requirements. Under the direction and on-the-floor guidance of the 2nd Shift Manufacturing Supervisor, the Manufacturing Technician IV will become qualified and independently capable of performing all aspects of internal cold manufacturing operations.  Such operations include, but are not limited to, receipt and transfer of materials and components into the manufacturing unit operation, component and equipment cleaning and preparation, operation of automated manufacturing equipment with good aseptic technique, completion of production transactions within the ERP system, completion of paper-based production records and forms in accordance with GDP. 3 – 5 years of experience in a pharmaceutical/biotech manufacturing or quality environment.salary: $55,000 - $62,000 per yearshift: Secondwork hours: 4 PM - 2:30 AMeducation: High` SchoolResponsibilitiesThis individual will support qualification activities and routine operator maintenance for manufacturing equipment, and will assist with inventory management in designated manufacturing areas.SkillsManufacturing (3 years of experience is required)GMP (1 year of experience is required)aseptic techniques (1 year of experience is preferred)Standard Operating Procedures (1 year of experience is preferred)Batch Records (1 year of experience is preferred)QualificationsYears of experience: 1 yearExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north billerica, massachusetts
    • permanent
    • $95,000 - $125,000 per year
    The objective of this position is to provide supervision of operations associated with pharmaceutical product manufacturing (non-radioactive) on the Billerica Campus, while ensuring that all operations comply with all GMP, OSHA and other regulatory requirements.  The Supervisor reports to the first Shift Manufacturing Manager and leads the execution of commercial pharmaceutical manufacturing according to standard operating procedures and production records in accordance with Current Good Manufacturing Practices (cGMP’s). The Supervisor is responsible for on-the-floor leadership of a team of manufacturing technicians whose primary focus is on execution of the manufacturing processes.  In addition to commercial production, the first shift Supervisor is responsible for compliance with internal and external guidance, technical assessment of the processes, innovation, and reliability. salary: $95,000 - $125,000 per yearshift: Firstwork hours: 8 AM - 4 PMeducation: BachelorResponsibilities Achieves the production schedule by coordinating materials, equipment, personnel, utilities and activities within his/her team, the second shift Supervisor and with partner organizations.  Ensures department goals and metrics are meeting or exceeding expectations.  Independently identifies deficiencies, creates and executes action plans to mitigate issues.  Build strong partnership with process support and facilities teams to ensure operations are supported by on-time maintenance and calibration.  Actively promotes a productive and cooperative environment by empowering resources to set and achieve goals together. SkillsManufacturing (2 years of experience is required)GMP (1 year of experience is required)Supervising (1 year of experience is required)Visual InspectionQualificationsYears of experience: 2 yearsExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    The objective of this position is to provide supervision of operations associated with pharmaceutical product manufacturing (non-radioactive) on the Billerica Campus, while ensuring that all operations comply with all GMP, OSHA and other regulatory requirements.  The Supervisor reports to the first Shift Manufacturing Manager and leads the execution of commercial pharmaceutical manufacturing according to standard operating procedures and production records in accordance with Current Good Manufacturing Practices (cGMP’s). The Supervisor is responsible for on-the-floor leadership of a team of manufacturing technicians whose primary focus is on execution of the manufacturing processes.  In addition to commercial production, the first shift Supervisor is responsible for compliance with internal and external guidance, technical assessment of the processes, innovation, and reliability. salary: $95,000 - $125,000 per yearshift: Firstwork hours: 8 AM - 4 PMeducation: BachelorResponsibilities Achieves the production schedule by coordinating materials, equipment, personnel, utilities and activities within his/her team, the second shift Supervisor and with partner organizations.  Ensures department goals and metrics are meeting or exceeding expectations.  Independently identifies deficiencies, creates and executes action plans to mitigate issues.  Build strong partnership with process support and facilities teams to ensure operations are supported by on-time maintenance and calibration.  Actively promotes a productive and cooperative environment by empowering resources to set and achieve goals together. SkillsManufacturing (2 years of experience is required)GMP (1 year of experience is required)Supervising (1 year of experience is required)Visual InspectionQualificationsYears of experience: 2 yearsExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • bedford, massachusetts
    • contract
    • $22 - $28.79 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Bedford, Massachusetts job type: Contract salary: $22.00 - 28.79 per hour work hours: 7 to 3 education: Bachelors   responsibilities: Makes buffers and sets up production runs. Prepares and tests tissue fractions.Interacts with Quality Assurance to identify non-conformance issues.Manufactures products using centrifugation, buffer extractions, filtration, and dialysis methods.Uses ERP system to perform production transactions.  qualifications: 1-3 years' experience preferable in a laboratory, life sciences environmentWilling to work as a team playerOpen to cross training and becoming multi-skilled.Lab experience working with lab equipment and tools5S and lean manufacturing knowledge (Preferred, but not required.)Able to take direction and work on production requirements as needed. (After training)Good working conditions. Work in clean rooms, general lab, and cold room ranging from 2 to minus 20 degrees Celsius, where specified PPE for each area is required. Frequently lifts and/or moves material and/or objects up to 25 pounds. May handle hazardous material in controlled environment.  skills: ERP System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Bedford, Massachusetts job type: Contract salary: $22.00 - 28.79 per hour work hours: 7 to 3 education: Bachelors   responsibilities: Makes buffers and sets up production runs. Prepares and tests tissue fractions.Interacts with Quality Assurance to identify non-conformance issues.Manufactures products using centrifugation, buffer extractions, filtration, and dialysis methods.Uses ERP system to perform production transactions.  qualifications: 1-3 years' experience preferable in a laboratory, life sciences environmentWilling to work as a team playerOpen to cross training and becoming multi-skilled.Lab experience working with lab equipment and tools5S and lean manufacturing knowledge (Preferred, but not required.)Able to take direction and work on production requirements as needed. (After training)Good working conditions. Work in clean rooms, general lab, and cold room ranging from 2 to minus 20 degrees Celsius, where specified PPE for each area is required. Frequently lifts and/or moves material and/or objects up to 25 pounds. May handle hazardous material in controlled environment.  skills: ERP System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lawrence, massachusetts
    • contract
    • $14.45 - $17 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lawrence, Massachusetts job type: Contract salary: $14.45 - 17.00 per hour work hours: 9 to 5 education: High School   responsibilities: Position Description: The Consumable tech will be responsible for manufacturing consumables according to SOP's , meeting company quality and efficiency standards. Position Requirements: - Work in consumable production with group lead or designated trainer - Possess basic manufacturing knowledge - Read, understand and execute SOP's - Basic computer skills - Additional duties as required or directed by the management team   qualifications: Qualifications: - Ability to stand for the duration of shift - Ability to lift 50 pounds - Good written and verbal communication skills - Attention to detail - ISO awareness Education High School Diploma or GED equivalent   skills: SOP Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lawrence, Massachusetts job type: Contract salary: $14.45 - 17.00 per hour work hours: 9 to 5 education: High School   responsibilities: Position Description: The Consumable tech will be responsible for manufacturing consumables according to SOP's , meeting company quality and efficiency standards. Position Requirements: - Work in consumable production with group lead or designated trainer - Possess basic manufacturing knowledge - Read, understand and execute SOP's - Basic computer skills - Additional duties as required or directed by the management team   qualifications: Qualifications: - Ability to stand for the duration of shift - Ability to lift 50 pounds - Good written and verbal communication skills - Attention to detail - ISO awareness Education High School Diploma or GED equivalent   skills: SOP Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lexington, massachusetts
    • contract
    • $25 - $30 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lexington, Massachusetts job type: Contract salary: $25 - 30 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Primary duties of this position will focus on the daily lab operations and execution of testing to support manufacturing operations. Testing may include but not limited to samples from drug substance and drug product, manufacturing, stability, raw materials and various protocol studies using test methods. The assays range from pH, enzyme concentration to more complex assays such as SDS silver Gels, PCR, DNA and enzyme activity. This position is expected to maintain operational and GMP readiness of the QC areas. In addition, this position will participate in more complex projects, Operational excellence initiatives and various quality systems. 65% of work: Testing execution35% of work: QC operations support which entails data review, data trending, OE/5S initiative, maintenance of equipment and reagents, reagent prep, lab house keeping, support for other QC groups if needed.  qualifications: Essential: Bachelors degree and minimum of 0-2 years related experienceDesired: GMP knowledge, work experience Knowledge: Limited use and/or application of basic principles, theories and concepts.Limited knowledge of industry practices and standards. Position requires critical thinking.Key Skills: MS Office, LIMS, SAP, Trackwise, EDMS, Compliance and strong science understandingSolve routine problems of limited scope and complexity following established policies and procedures. Works on problems of limited scope. Follows standard practices and procedures in analyzing situations of data from which answers can be readily obtained. Builds stable working relationships internally.The following physical abilities are required in order to fulfill the job duties:Repetitive bendings and reaching to setup and break down equipmentAbility to work around chemicalsAbility to wear personal protective equipment such as gloves, gowning, and respiratory protection in some casesAbility to walk and stand for periods of time Individual may be required to participate in environment chamber monitoring program which would include the use of an on- call mobile phone as well as on site support during non-business hours  skills: Quality control, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lexington, Massachusetts job type: Contract salary: $25 - 30 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Primary duties of this position will focus on the daily lab operations and execution of testing to support manufacturing operations. Testing may include but not limited to samples from drug substance and drug product, manufacturing, stability, raw materials and various protocol studies using test methods. The assays range from pH, enzyme concentration to more complex assays such as SDS silver Gels, PCR, DNA and enzyme activity. This position is expected to maintain operational and GMP readiness of the QC areas. In addition, this position will participate in more complex projects, Operational excellence initiatives and various quality systems. 65% of work: Testing execution35% of work: QC operations support which entails data review, data trending, OE/5S initiative, maintenance of equipment and reagents, reagent prep, lab house keeping, support for other QC groups if needed.  qualifications: Essential: Bachelors degree and minimum of 0-2 years related experienceDesired: GMP knowledge, work experience Knowledge: Limited use and/or application of basic principles, theories and concepts.Limited knowledge of industry practices and standards. Position requires critical thinking.Key Skills: MS Office, LIMS, SAP, Trackwise, EDMS, Compliance and strong science understandingSolve routine problems of limited scope and complexity following established policies and procedures. Works on problems of limited scope. Follows standard practices and procedures in analyzing situations of data from which answers can be readily obtained. Builds stable working relationships internally.The following physical abilities are required in order to fulfill the job duties:Repetitive bendings and reaching to setup and break down equipmentAbility to work around chemicalsAbility to wear personal protective equipment such as gloves, gowning, and respiratory protection in some casesAbility to walk and stand for periods of time Individual may be required to participate in environment chamber monitoring program which would include the use of an on- call mobile phone as well as on site support during non-business hours  skills: Quality control, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts
    • contract
    • $40 - $45.68 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $40.00 - 45.68 per hour work hours: 9 to 5 education: Bachelors   responsibilities: We are looking for an experienced individual with a strong background in histology to join our dynamic team of histotechnologists and pathologists as part of nonclinical safety assessment of new drug candidates. Perform basic histology procedures (e.g. handling unfixed and fixed human and animal tissues, accurate slide and cassette labeling, tissue trimming, processing, embedding, paraffin and frozen microtomy, routine H&E staining and special histochemical staining, coverslipping, archiving of specimens)Ensure and maintain preanalytical specimen handling integrity and quality to meet molecular pathology laboratory standards.Maintain adequate stock and efficient use of supplies necessary for performing all procedures, and preparation of reagents as required.Maintain laboratory equipment and assist with identification and execution of process improvement.Perform routine scanning of stained slides using slide image acquisition systems (e.g. Aperio ScanScope/Versa; Phillips Ultra Fast Scanner, or similar) and, manage the slide image database (e.g. Aperio eSlide manager; Phillips Philips IntelliSite Solution, or similar).Adhere to chemical agent, facility, and bio-facility safety requirements.Understand and follow Standard Operating Procedures (SOPs) and Study Protocol requirements for all laboratory assigned activities.Maintain proper documentation, archiving and routine quality control on all generated specimens and data in compliance with corporate policies and practices.Demonstrate a clear interest and ability in learning new skills along with the ability to be organized, multitask, communicate effectively with a team and diverse individuals.  qualifications: Minimum BS or MS degree in a Biological or Life Science.2-4+ years of relevant clinical or research histotechnology laboratory experience.The ideal candidate will have extensive experience with histology.Familiarity with immunohistochemistry, in situ hybridization, with the ability to independently troubleshoot and solve technical problems are desirable.Successful candidates will be able to work within a matrixed organization, across multiple reporting lines and functional areas.The position is within a laboratory in an expansion phase, with expectations for excellent interpersonal skills supporting and maintaining the current highly collaborative environment.Demonstrated strong background in IHC/ISH techniques, ASCP qualification in immunohistochemistry (QIHC) preferred.Necropsy experience is desirable.American Society for Clinical Pathology (ASCP) certification: HT (desirable), HTL (preferred).Experience with collection and documentation of research data in compliance with Good Laboratory Practices (GLPs) is desirable.  skills: SOP, GLP (Good Laboratory Practice), Sample Preparation, Sample Testing, Sanitation Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $40.00 - 45.68 per hour work hours: 9 to 5 education: Bachelors   responsibilities: We are looking for an experienced individual with a strong background in histology to join our dynamic team of histotechnologists and pathologists as part of nonclinical safety assessment of new drug candidates. Perform basic histology procedures (e.g. handling unfixed and fixed human and animal tissues, accurate slide and cassette labeling, tissue trimming, processing, embedding, paraffin and frozen microtomy, routine H&E staining and special histochemical staining, coverslipping, archiving of specimens)Ensure and maintain preanalytical specimen handling integrity and quality to meet molecular pathology laboratory standards.Maintain adequate stock and efficient use of supplies necessary for performing all procedures, and preparation of reagents as required.Maintain laboratory equipment and assist with identification and execution of process improvement.Perform routine scanning of stained slides using slide image acquisition systems (e.g. Aperio ScanScope/Versa; Phillips Ultra Fast Scanner, or similar) and, manage the slide image database (e.g. Aperio eSlide manager; Phillips Philips IntelliSite Solution, or similar).Adhere to chemical agent, facility, and bio-facility safety requirements.Understand and follow Standard Operating Procedures (SOPs) and Study Protocol requirements for all laboratory assigned activities.Maintain proper documentation, archiving and routine quality control on all generated specimens and data in compliance with corporate policies and practices.Demonstrate a clear interest and ability in learning new skills along with the ability to be organized, multitask, communicate effectively with a team and diverse individuals.  qualifications: Minimum BS or MS degree in a Biological or Life Science.2-4+ years of relevant clinical or research histotechnology laboratory experience.The ideal candidate will have extensive experience with histology.Familiarity with immunohistochemistry, in situ hybridization, with the ability to independently troubleshoot and solve technical problems are desirable.Successful candidates will be able to work within a matrixed organization, across multiple reporting lines and functional areas.The position is within a laboratory in an expansion phase, with expectations for excellent interpersonal skills supporting and maintaining the current highly collaborative environment.Demonstrated strong background in IHC/ISH techniques, ASCP qualification in immunohistochemistry (QIHC) preferred.Necropsy experience is desirable.American Society for Clinical Pathology (ASCP) certification: HT (desirable), HTL (preferred).Experience with collection and documentation of research data in compliance with Good Laboratory Practices (GLPs) is desirable.  skills: SOP, GLP (Good Laboratory Practice), Sample Preparation, Sample Testing, Sanitation Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts
    • contract
    • $28.64 - $33.69 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $28.64 - 33.69 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Maintains and develops effective documentation systems appropriate for a research setting.Coordinates and ensures appropriate documentation for the Vaccine Research and Analytics laboratory.Facilitate and oversee the coordination, planning, assembly, writing, editing, and quality control of written research findings (reports, abstracts, manuscripts, systematic reviews, presentations, etc.) or regulatory documents (protocols, investigator brochures, study reports, etc.). Ensure data and reports are in compliance with regulatory standards, applicable SOPs, policies, procedures.Work with authors/technical specialists to coordinate the completion of specialized content, to translate, write, edit and/or proof data and content (exhibits, illustrations, tables, and appendices) for publication into finished documents appropriate for the stated audience. Participate in quality control review for documents written by other authors when requested.Write and review standard operating procedures (SOPs), laboratory procedures, equipment instructions, knowledge- based documents and business policies.Generate document templates and laboratory and equipment logs for general use.Manage templates and document versions in an electronic document management system (EDMS).Manage documents and training in a learning management system (LMS), to help plan, deliver and assess competencies.Develop an archiving plan and prepare records for archving in an electronic records management system (ERMS).Submit data and reports to Regulatory for inclusion in dossiers.Train technical staff and management in quality and documentation procedures, including good documentation practices, handling and review of electronic laboratory notebooks, data and reports.  qualifications: B.S degree in a scientific disciplineAt least 6 years laboratory experience, preferably in a clinical testing or analytical laboratory, Quality, or R&DMust have excellent written communication skills and attention to detail related to consistency, grammar, syntax, and accuracy.Must have experience working in a GXP environmentMust have experience writing and reviewing technical documentation, ideally have experience with advanced functions of Microsoft Word.Experience working in a GXP environment is preferred.Familiarity with regulatory processing and submissions is desirable.Experience with Electronic Document and Learning Management Systems is desirable.Experience working with and training cross functional groups. Must be creatively open to new ideas and methods and work with a spirit of continuous improvement and innovation.Ability to identify, report, and seek prompt corrections as they arise.Manual dexterity required to operate office equipment (i.e. computers, phones, etc.).  skills: SOP, MS-WORD, MS-EXCEL, MS-Powerpoint, LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $28.64 - 33.69 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Maintains and develops effective documentation systems appropriate for a research setting.Coordinates and ensures appropriate documentation for the Vaccine Research and Analytics laboratory.Facilitate and oversee the coordination, planning, assembly, writing, editing, and quality control of written research findings (reports, abstracts, manuscripts, systematic reviews, presentations, etc.) or regulatory documents (protocols, investigator brochures, study reports, etc.). Ensure data and reports are in compliance with regulatory standards, applicable SOPs, policies, procedures.Work with authors/technical specialists to coordinate the completion of specialized content, to translate, write, edit and/or proof data and content (exhibits, illustrations, tables, and appendices) for publication into finished documents appropriate for the stated audience. Participate in quality control review for documents written by other authors when requested.Write and review standard operating procedures (SOPs), laboratory procedures, equipment instructions, knowledge- based documents and business policies.Generate document templates and laboratory and equipment logs for general use.Manage templates and document versions in an electronic document management system (EDMS).Manage documents and training in a learning management system (LMS), to help plan, deliver and assess competencies.Develop an archiving plan and prepare records for archving in an electronic records management system (ERMS).Submit data and reports to Regulatory for inclusion in dossiers.Train technical staff and management in quality and documentation procedures, including good documentation practices, handling and review of electronic laboratory notebooks, data and reports.  qualifications: B.S degree in a scientific disciplineAt least 6 years laboratory experience, preferably in a clinical testing or analytical laboratory, Quality, or R&DMust have excellent written communication skills and attention to detail related to consistency, grammar, syntax, and accuracy.Must have experience working in a GXP environmentMust have experience writing and reviewing technical documentation, ideally have experience with advanced functions of Microsoft Word.Experience working in a GXP environment is preferred.Familiarity with regulatory processing and submissions is desirable.Experience with Electronic Document and Learning Management Systems is desirable.Experience working with and training cross functional groups. Must be creatively open to new ideas and methods and work with a spirit of continuous improvement and innovation.Ability to identify, report, and seek prompt corrections as they arise.Manual dexterity required to operate office equipment (i.e. computers, phones, etc.).  skills: SOP, MS-WORD, MS-EXCEL, MS-Powerpoint, LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lexington, massachusetts
    • temporary
    • $28 - $30 per hour
    We are currently hiring for a QC Analyst at Takeda Pharmaceuticals, based in Lexington, MA.  This individual will support rhASA D/TAK-611 QC MV as a part of the QC HPLC team. This is a 9-month contract to start with the potential to extend from there.  Please reach out to ashley.cross@randstadusa.com with any questions!salary: $28 - $30 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilitiesRole is responsible for HPLC laboratories performing a broad range of analytical based techniques such as SE-HPLC, RP-HPLC, IEX, CE-SDS, glycan and peptide analyses in order to support in-process, release and stability testing. Support commercial and clinical testing for defined site-based and external programs, as well as method transfer and validation- introduction of new equipment and technology to improve sustainability and compliance is expected Provide support for Quality projects and implementation of operational excellence initiatives Areas of focus on techniques such as HPLC and SDS-PAGE for purity, identity, potency and charged heterogeneity. Perform and troubleshoot HPLC based assays (SE-HPLC, IEX, RP-HPLC, CE-SDS, Peptide Mapping, and Glycan Mapping) of release and stability Execute and lead method qualification and validation assays as needed Perform and lead OOT, OOS, GMP Investigations, data analysis, deviation and data trending Maintain GMP condition of the lab The essential functions of this role include:working in a smoke free environmentSkillsQuality ControlHPLCSDS-PAGEQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    We are currently hiring for a QC Analyst at Takeda Pharmaceuticals, based in Lexington, MA.  This individual will support rhASA D/TAK-611 QC MV as a part of the QC HPLC team. This is a 9-month contract to start with the potential to extend from there.  Please reach out to ashley.cross@randstadusa.com with any questions!salary: $28 - $30 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilitiesRole is responsible for HPLC laboratories performing a broad range of analytical based techniques such as SE-HPLC, RP-HPLC, IEX, CE-SDS, glycan and peptide analyses in order to support in-process, release and stability testing. Support commercial and clinical testing for defined site-based and external programs, as well as method transfer and validation- introduction of new equipment and technology to improve sustainability and compliance is expected Provide support for Quality projects and implementation of operational excellence initiatives Areas of focus on techniques such as HPLC and SDS-PAGE for purity, identity, potency and charged heterogeneity. Perform and troubleshoot HPLC based assays (SE-HPLC, IEX, RP-HPLC, CE-SDS, Peptide Mapping, and Glycan Mapping) of release and stability Execute and lead method qualification and validation assays as needed Perform and lead OOT, OOS, GMP Investigations, data analysis, deviation and data trending Maintain GMP condition of the lab The essential functions of this role include:working in a smoke free environmentSkillsQuality ControlHPLCSDS-PAGEQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts (remote)
    • contract
    • $24.13 - $28.38 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team!   location: Telecommute job type: Contract salary: $24.13 - 28.38 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Process import/export trade compliance clearance of cross-border shipments in Global Trade Management system (Oracle module)Maintenance of GTM systemsCommunication on shipments processing with different functions and customs brokersPre-validation and post audit of documentation related to customs clearancesVarious administrative support activities  qualifications: Experience with customs entry processes and data managementExperience preparing import licenses and permits with different government agencies (e.g. Customs, FDA, USDA, Aphis)Experience working with customs brokers. Background in entry writing and customs clearance is a plus.Experience with regulated industries (e.g. food, medical devices, pharma, etc.)Availability to work in US ET time zone, as well as early calls to coordinate with Europe locations.  skills: Import/Export Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team!   location: Telecommute job type: Contract salary: $24.13 - 28.38 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Process import/export trade compliance clearance of cross-border shipments in Global Trade Management system (Oracle module)Maintenance of GTM systemsCommunication on shipments processing with different functions and customs brokersPre-validation and post audit of documentation related to customs clearancesVarious administrative support activities  qualifications: Experience with customs entry processes and data managementExperience preparing import licenses and permits with different government agencies (e.g. Customs, FDA, USDA, Aphis)Experience working with customs brokers. Background in entry writing and customs clearance is a plus.Experience with regulated industries (e.g. food, medical devices, pharma, etc.)Availability to work in US ET time zone, as well as early calls to coordinate with Europe locations.  skills: Import/Export Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lexington, massachusetts
    • contract
    • $28 - $29 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you!   location: Lexington, Massachusetts job type: Contract salary: $28 - 29 per hour work hours: 3 to 11 education: High School   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. · Execution of critical and routine activities in support of production · Perform Batch Record, Log Book and Form Prep requests · Enter data in the Laboratory Information Management System (LIMS) , MODA and or other business functions · Troubleshoot and resolve basic process related issues · Recognize and escalate deviation · Review GMP documentation · Sample preparation and testing · Identify changes needed to documentation · Participate in tiered visual management system and support CI initiatives · Complete required training on time · Initiate work orders · Assemble and disassemble process equipment · Perform scheduled cleaning of equipment · Perform standardization of equipment · Support change over activities · Execution of equipment and process qualifications as well as validation   qualifications: · Takes the initiative to openly express ideas and concerns · Establishes credibility and acts responsibly to earn the confidence, trust and respect of others · Recognizes and acknowledges others' contributions to team success · Proactively assists others in accomplishing work · Builds and maintains productive relationships based on mutual trust and respect · Professionally communicates with all business partners · Establishes challenging goals and holds self-accountable for achieving them · Effectively manages multiple assignments and competing priorities by maximizing time, being well organized and utilizing available resources · Ensures delivery of accurate and complete work within designated timelines · Understands and follows the Code of Conduct, policies, and procedures relevant to job accountabilities · Effectively demonstrates an understanding of the company's core business in meeting the needs of others · Demonstrates ability to solve problems by analyzing issues and making informed recommendations · Adjusts work by organizing and prioritizing tasks in the face of changing business needs. · Demonstrates a professional approach in adapting to change · Adapts work products, processes and services in response to changes in the business environment · Listens carefully and is receptive to feedback from others · Demonstrates a willingness to admit one's mistakes and modify approach to ensure a positive outcome · Demonstrates composure under trying circumstances and approaches problems professionally · Actively seeks opportunities for personal growth and development and monitors progress toward achieving development goals · Consistently utilizes available resources to acquire, develop and apply new skills and knowledge · Responds to feedback by capitalizing on strengths and building upon areas of improvement for the benefit of the organization   skills: SOP, Laboratory Information Management Systems (LIMS), ICH Regulations, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you!   location: Lexington, Massachusetts job type: Contract salary: $28 - 29 per hour work hours: 3 to 11 education: High School   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. · Execution of critical and routine activities in support of production · Perform Batch Record, Log Book and Form Prep requests · Enter data in the Laboratory Information Management System (LIMS) , MODA and or other business functions · Troubleshoot and resolve basic process related issues · Recognize and escalate deviation · Review GMP documentation · Sample preparation and testing · Identify changes needed to documentation · Participate in tiered visual management system and support CI initiatives · Complete required training on time · Initiate work orders · Assemble and disassemble process equipment · Perform scheduled cleaning of equipment · Perform standardization of equipment · Support change over activities · Execution of equipment and process qualifications as well as validation   qualifications: · Takes the initiative to openly express ideas and concerns · Establishes credibility and acts responsibly to earn the confidence, trust and respect of others · Recognizes and acknowledges others' contributions to team success · Proactively assists others in accomplishing work · Builds and maintains productive relationships based on mutual trust and respect · Professionally communicates with all business partners · Establishes challenging goals and holds self-accountable for achieving them · Effectively manages multiple assignments and competing priorities by maximizing time, being well organized and utilizing available resources · Ensures delivery of accurate and complete work within designated timelines · Understands and follows the Code of Conduct, policies, and procedures relevant to job accountabilities · Effectively demonstrates an understanding of the company's core business in meeting the needs of others · Demonstrates ability to solve problems by analyzing issues and making informed recommendations · Adjusts work by organizing and prioritizing tasks in the face of changing business needs. · Demonstrates a professional approach in adapting to change · Adapts work products, processes and services in response to changes in the business environment · Listens carefully and is receptive to feedback from others · Demonstrates a willingness to admit one's mistakes and modify approach to ensure a positive outcome · Demonstrates composure under trying circumstances and approaches problems professionally · Actively seeks opportunities for personal growth and development and monitors progress toward achieving development goals · Consistently utilizes available resources to acquire, develop and apply new skills and knowledge · Responds to feedback by capitalizing on strengths and building upon areas of improvement for the benefit of the organization   skills: SOP, Laboratory Information Management Systems (LIMS), ICH Regulations, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • woburn, massachusetts
    • permanent
    • $60,000 - $70,000 per year
    job summary: Woburn MA based cryogenics research company who offers cryogenic systems for a broad range of applications, with cooling provided by liquid helium, liquid nitrogen or mechanical refrigerators is actively seeking (1) highly skilled Senior Laboratory Technician to start immediately within the next 2-3wks. Working hours will be hours are 6:45am - 3:15pm. The Lab Technician will be responsible for the hands-on assembly of Ultra-low temperature cryogenic products including dilution refrigerator system and He-3 cryostat. Ideal candidate should have knowledge of wiring, soldering, reading, and working from mechanical assembly drawings and/or solid work. Working with mass spectrometer leak detectors, vacuum pumps, low-temperature thermometers transferring cryogens and trouble-shooting cryogenic systems. Basic electrical and electronics knowledge. Good experience working with laboratory tools and facilities. This position requires good manual dexterity and working with small parts and fine wires. Great location off routes 93 and 95, also commuter rail access from Lowell and Boston. Plenty of great shopping spots, restaurants and a easy commute to tax-free New Hampshire!!   location: Woburn, Massachusetts job type: Permanent salary: $60,000 - 70,000 per year work hours: 7 to 3 education: Associate   responsibilities: Perform all functions of lab technicianPerform all phases of assembly with minimal supervision and ≥80% efficiency on the following systems: All models of He-3 cryostatAll models of dilution refrigerator systemsAll gas handling systems for continuous flow type cryostats Able to create a reliable vacuum seal, such as O-ring seal, indium seal, CF seal, etc.Able to charge and decontaminate a cryocooler/compressor systemAble to train other Lab TechniciansNo supervisory responsibilities for this position.Basic vacuum knowledgeFamiliar with vacuum greaseBeing able to do perform basic vacuum pump serviceSkillful for leak checkingKnowledge on epoxy Able to read and understand the epoxy matrixAble to use 5 minute, Stycast 2850, Araldite epoxy etc.Understand different function for different type of epoxies Knowledge on electricity Understand Ohm's law (V=IR) and powerProper use of DMMKnow difference between AC and DCAware of different wall socket voltages (120 VAC, 220 VAC, 380 VAC, and 480 VAC)Aware of two frequencies (60Hz, 50Hz) Aware of two phases of power (single, three)  qualifications: Minimum Experience: 2 yearsEducation Requirements: High School Diploma, Trade/Technical SchoolSufficient computer skills for the following:Read SW model or e-drawingRead BOM and search parts  skills: MS-WORD, MS-Project, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice), Manufacturing Operations Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Woburn MA based cryogenics research company who offers cryogenic systems for a broad range of applications, with cooling provided by liquid helium, liquid nitrogen or mechanical refrigerators is actively seeking (1) highly skilled Senior Laboratory Technician to start immediately within the next 2-3wks. Working hours will be hours are 6:45am - 3:15pm. The Lab Technician will be responsible for the hands-on assembly of Ultra-low temperature cryogenic products including dilution refrigerator system and He-3 cryostat. Ideal candidate should have knowledge of wiring, soldering, reading, and working from mechanical assembly drawings and/or solid work. Working with mass spectrometer leak detectors, vacuum pumps, low-temperature thermometers transferring cryogens and trouble-shooting cryogenic systems. Basic electrical and electronics knowledge. Good experience working with laboratory tools and facilities. This position requires good manual dexterity and working with small parts and fine wires. Great location off routes 93 and 95, also commuter rail access from Lowell and Boston. Plenty of great shopping spots, restaurants and a easy commute to tax-free New Hampshire!!   location: Woburn, Massachusetts job type: Permanent salary: $60,000 - 70,000 per year work hours: 7 to 3 education: Associate   responsibilities: Perform all functions of lab technicianPerform all phases of assembly with minimal supervision and ≥80% efficiency on the following systems: All models of He-3 cryostatAll models of dilution refrigerator systemsAll gas handling systems for continuous flow type cryostats Able to create a reliable vacuum seal, such as O-ring seal, indium seal, CF seal, etc.Able to charge and decontaminate a cryocooler/compressor systemAble to train other Lab TechniciansNo supervisory responsibilities for this position.Basic vacuum knowledgeFamiliar with vacuum greaseBeing able to do perform basic vacuum pump serviceSkillful for leak checkingKnowledge on epoxy Able to read and understand the epoxy matrixAble to use 5 minute, Stycast 2850, Araldite epoxy etc.Understand different function for different type of epoxies Knowledge on electricity Understand Ohm's law (V=IR) and powerProper use of DMMKnow difference between AC and DCAware of different wall socket voltages (120 VAC, 220 VAC, 380 VAC, and 480 VAC)Aware of two frequencies (60Hz, 50Hz) Aware of two phases of power (single, three)  qualifications: Minimum Experience: 2 yearsEducation Requirements: High School Diploma, Trade/Technical SchoolSufficient computer skills for the following:Read SW model or e-drawingRead BOM and search parts  skills: MS-WORD, MS-Project, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice), Manufacturing Operations Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts (remote)
    • contract
    • $75 - $90 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $75 - 90 per hour work hours: 9 to 5 education: Bachelors   responsibilities: This position will primarily be responsible for the following activities under the guidance of the Patient Engagement Disease Unit Leads and the Head of Program and Study Leadership: support programs and teams by developing a strategy for the recruitment and retention of patients- provide input to the study team by identifying key issues and barriers to successful recruitment and retention- including digital strategies and health equality needsSupport study teams regarding the assessment/ incorporation of patient and/or caregiver input into Company protocols to influence study design with the goal of generating data to support executable, patient friendly study designs and assessments.Include recruitment strategies to support underserved/underrepresented populations access to clinical trialsIntegrate Patient Engagement efforts with other key groups eg Company Patient AdvocacyAlong with our CRO provide vendor oversight of recruitment and retention vendorsRole will include maintaining trackers and metrics to regarding ROI of recruitment tactics.Role will liaise with other groups outside GCO such as R&D business operations, procurement, sourcing, finance, Legal as needed.   qualifications: Approximately 8 years of clinical research / project management experience in the sponsor or CRO setting.Must have at least 2 years' experience of working in a similar Patient Engagement role in Clinical Trials.Risk management, mitigation and problem-solvingFamiliarity with GCPProven ability to multi-task and thrive in a fast-paced environmentWorks and meets deadlines while being detailed orientedSelf-motivatorDedication to quality in all work tasks and deliverablesAbility to work effectively in cross-functional and global teams  skills: MS-WORD, MS-EXCEL, GCP (Good Clinical Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $75 - 90 per hour work hours: 9 to 5 education: Bachelors   responsibilities: This position will primarily be responsible for the following activities under the guidance of the Patient Engagement Disease Unit Leads and the Head of Program and Study Leadership: support programs and teams by developing a strategy for the recruitment and retention of patients- provide input to the study team by identifying key issues and barriers to successful recruitment and retention- including digital strategies and health equality needsSupport study teams regarding the assessment/ incorporation of patient and/or caregiver input into Company protocols to influence study design with the goal of generating data to support executable, patient friendly study designs and assessments.Include recruitment strategies to support underserved/underrepresented populations access to clinical trialsIntegrate Patient Engagement efforts with other key groups eg Company Patient AdvocacyAlong with our CRO provide vendor oversight of recruitment and retention vendorsRole will include maintaining trackers and metrics to regarding ROI of recruitment tactics.Role will liaise with other groups outside GCO such as R&D business operations, procurement, sourcing, finance, Legal as needed.   qualifications: Approximately 8 years of clinical research / project management experience in the sponsor or CRO setting.Must have at least 2 years' experience of working in a similar Patient Engagement role in Clinical Trials.Risk management, mitigation and problem-solvingFamiliarity with GCPProven ability to multi-task and thrive in a fast-paced environmentWorks and meets deadlines while being detailed orientedSelf-motivatorDedication to quality in all work tasks and deliverablesAbility to work effectively in cross-functional and global teams  skills: MS-WORD, MS-EXCEL, GCP (Good Clinical Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts
    • contract
    • $83.42 - $98.14 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $83.42 - 98.14 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Under the direction of the Director of Regulatory Affairs direct and manage Regulatory Affairs activities for developing a Core Dossier for Module 3 and preparing Module 3 documents to support Marketing Authorization Applications in Japan and Brazil. Provide support to other HA interactions as required. Provide regulatory support, guidance and expertise to internal groups such as product development, QA, QC and manufacturing teams to ensure that all applicable regulatory requirements are considered and appropriately incorporated into submissions for marketing authorizations.Provide Reg CMC support for development programs to ensure that products are developed and manufactured in compliance with appropriate regulations and guidelines so that they be studied and marketed as planned.Manage preparation of Core Dossier, Japan and Brazil applications in a timely manner to meet corporate objectives. Collaborate with EU & International regulatory colleagues to ensure global perspective and provide support in the preparation of EU and International regulatory documentation in a timely manner to meet corporate objectives. 30%: Develop global CMC Core Dossier for Module 3 20%: Prepare Module 3 Marketing Authorization Application for Japan 30%: Prepare Module 3 Marketing Authorization Application for Brazil. 10%: Review and approve technical documentation including technology transfer protocols, validation protocols, technical reports, manufacturing and labeling information to assure conformance with regulations; and regulatory guidelines. 10%: Provide CMC regulatory guidance to project / product teams.   qualifications: B.A. / B.A./ M.S. / Ph.D. in biochemistry, chemistry, biology or related pharmaceutical field. Minimum of 4 years experience in pharmaceutical product development including significant experience in CMC regulatory affairs with a strong biologics background or equivalent.Experience in directing interactions with regulatory authorities desired.Knowledgeable in ICH and FDA guidelines relevant to CMC aspects of product development and maintenance. Significant coordination with cross-functional teams internally and regulatory authorities externally.   skills: CMC, FDA, GCP (Good Clinical Practice), Regulatory Affairs Operations, Regulatory Affairs Strategy, Submissions, ICH Regulations Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $83.42 - 98.14 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Under the direction of the Director of Regulatory Affairs direct and manage Regulatory Affairs activities for developing a Core Dossier for Module 3 and preparing Module 3 documents to support Marketing Authorization Applications in Japan and Brazil. Provide support to other HA interactions as required. Provide regulatory support, guidance and expertise to internal groups such as product development, QA, QC and manufacturing teams to ensure that all applicable regulatory requirements are considered and appropriately incorporated into submissions for marketing authorizations.Provide Reg CMC support for development programs to ensure that products are developed and manufactured in compliance with appropriate regulations and guidelines so that they be studied and marketed as planned.Manage preparation of Core Dossier, Japan and Brazil applications in a timely manner to meet corporate objectives. Collaborate with EU & International regulatory colleagues to ensure global perspective and provide support in the preparation of EU and International regulatory documentation in a timely manner to meet corporate objectives. 30%: Develop global CMC Core Dossier for Module 3 20%: Prepare Module 3 Marketing Authorization Application for Japan 30%: Prepare Module 3 Marketing Authorization Application for Brazil. 10%: Review and approve technical documentation including technology transfer protocols, validation protocols, technical reports, manufacturing and labeling information to assure conformance with regulations; and regulatory guidelines. 10%: Provide CMC regulatory guidance to project / product teams.   qualifications: B.A. / B.A./ M.S. / Ph.D. in biochemistry, chemistry, biology or related pharmaceutical field. Minimum of 4 years experience in pharmaceutical product development including significant experience in CMC regulatory affairs with a strong biologics background or equivalent.Experience in directing interactions with regulatory authorities desired.Knowledgeable in ICH and FDA guidelines relevant to CMC aspects of product development and maintenance. Significant coordination with cross-functional teams internally and regulatory authorities externally.   skills: CMC, FDA, GCP (Good Clinical Practice), Regulatory Affairs Operations, Regulatory Affairs Strategy, Submissions, ICH Regulations Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lexington, massachusetts
    • contract
    • $80.20 - $94.35 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lexington, Massachusetts job type: Contract salary: $80.20 - 94.35 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Materials & Process Scientist for the Raw Material Alternatives Taskforce will act as a technical SME and facilitator to develop a consistent approach for the global implementation of alternative suppliers of raw materials used in manufacturing. He/she will be responsible for developing technical plans to evaluate alternate materials, translating supply mitigation strategies into executable implementation work plans, and partnering with personnel at manufacturing sites to understand and evaluate site-specific material requirements. He/She will be the liaison between Technical process experts (Global manufacturing sciences, local manufacturing sciences, and material qualification) as well as the manufacturing and Quality organizations to ensure implementation progression and uninterrupted manufacturing. This individual will provide global value by centralizing of non-product- and non-site-specific tasks. This is an individual contributor role with cross-functional leadership responsibilities. Compare current and proposed new raw materials, and identify differences and risks to product quality, process performance, and patient safetyCollaborate cross functionally to define technical requirements and activities needed to implement alternative raw materials based on category of material.Standardize the implementation approach of alternatives across multiple manufacturing sites and impacted products.Translate supply risks and mitigation proposals into executable tasks and implementation plans at manufacturing site level.Serve as the communication pathway between CMC teams and Local sites to project governance for reporting project progress, risks, and issues.  qualifications: Required BS in engineering, life sciences, or related field with a minimum 10 years' experience, MS with a minimum of 8 years' experience, or PhD with 2-5 years' experience in pharmaceutical development and manufacturing (preferred), or experience in medical devices or other adjacent industriesExperience working in a GMP environmentStrong project leadership/project management experience with a successful track record of change management projects and processes.Strong communication and interpersonal skills.Ability to collaborate and work cross-functionally in a global environment. Preferred Expertise in one or more of the following: single use systems, filters, chromatography resins, chemicals, cell culture media, excipients, elemental impurities analysis, extractable and leachables assessments, dual sourcing of raw materials.Working knowledge of GMP biologics manufacturing processes and a comprehensive understanding of dependencies between materials, processes, and final product.High level of professionalism and business etiquette when communicating with cross-functional teams, and external suppliers.Ability to manage numerous priorities simultaneouslyLead projects and meetings effectively.Ability to influence and interact well with others (customers, peers and others in more senior positions)Proficient in the use of Microsoft Office including Word, Excel, Visio, and Power PointApply industry guidelines and applicable technology standards to decision making processesProvides leadership on cross-functional teamsProvides leadership to drive highly complex projects including ones that span multiple sites and productsConsult and collaborate with cross-functional teams including but not limited to Global Process Sciences, local Manufacturing Sciences, Material Qualification, Quality, Manufacturing, Engineering, Procurement & Supply chain.Act as a representative in cross-functional teams, leading the global implementation of alternative suppliers of raw materials used in manufacturing. Serve as the communication pathway between CMC teams and Local sites to project governance for reporting project progress, risks, and issues.  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, Chromatography, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lexington, Massachusetts job type: Contract salary: $80.20 - 94.35 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Materials & Process Scientist for the Raw Material Alternatives Taskforce will act as a technical SME and facilitator to develop a consistent approach for the global implementation of alternative suppliers of raw materials used in manufacturing. He/she will be responsible for developing technical plans to evaluate alternate materials, translating supply mitigation strategies into executable implementation work plans, and partnering with personnel at manufacturing sites to understand and evaluate site-specific material requirements. He/She will be the liaison between Technical process experts (Global manufacturing sciences, local manufacturing sciences, and material qualification) as well as the manufacturing and Quality organizations to ensure implementation progression and uninterrupted manufacturing. This individual will provide global value by centralizing of non-product- and non-site-specific tasks. This is an individual contributor role with cross-functional leadership responsibilities. Compare current and proposed new raw materials, and identify differences and risks to product quality, process performance, and patient safetyCollaborate cross functionally to define technical requirements and activities needed to implement alternative raw materials based on category of material.Standardize the implementation approach of alternatives across multiple manufacturing sites and impacted products.Translate supply risks and mitigation proposals into executable tasks and implementation plans at manufacturing site level.Serve as the communication pathway between CMC teams and Local sites to project governance for reporting project progress, risks, and issues.  qualifications: Required BS in engineering, life sciences, or related field with a minimum 10 years' experience, MS with a minimum of 8 years' experience, or PhD with 2-5 years' experience in pharmaceutical development and manufacturing (preferred), or experience in medical devices or other adjacent industriesExperience working in a GMP environmentStrong project leadership/project management experience with a successful track record of change management projects and processes.Strong communication and interpersonal skills.Ability to collaborate and work cross-functionally in a global environment. Preferred Expertise in one or more of the following: single use systems, filters, chromatography resins, chemicals, cell culture media, excipients, elemental impurities analysis, extractable and leachables assessments, dual sourcing of raw materials.Working knowledge of GMP biologics manufacturing processes and a comprehensive understanding of dependencies between materials, processes, and final product.High level of professionalism and business etiquette when communicating with cross-functional teams, and external suppliers.Ability to manage numerous priorities simultaneouslyLead projects and meetings effectively.Ability to influence and interact well with others (customers, peers and others in more senior positions)Proficient in the use of Microsoft Office including Word, Excel, Visio, and Power PointApply industry guidelines and applicable technology standards to decision making processesProvides leadership on cross-functional teamsProvides leadership to drive highly complex projects including ones that span multiple sites and productsConsult and collaborate with cross-functional teams including but not limited to Global Process Sciences, local Manufacturing Sciences, Material Qualification, Quality, Manufacturing, Engineering, Procurement & Supply chain.Act as a representative in cross-functional teams, leading the global implementation of alternative suppliers of raw materials used in manufacturing. Serve as the communication pathway between CMC teams and Local sites to project governance for reporting project progress, risks, and issues.  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, Chromatography, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts
    • contract
    • $30 - $34.60 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $30.00 - 34.60 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The company is seeking a highly motivated biologist to join the Bioassays & HTS team in support of Gene Therapy projects within the Biotherapeutic & Medicinal Sciences department. Our group develops small format assays, executes high throughput screens (HTS) and the subsequent assessment of candidate molecules as part of a collaborative team of scientists. The primary responsibilities for this position are development and implementation of innovative cell-based assays using high throughput technologies, use of data analysis tools to assess biological activity and advance portfolio projects. The candidate must have experience with in vitro cell culture, use of primary cells plus experience with a preference for experience in neurobiology. The successful candidate will accomplish our mission through innovation, open communication, teamwork, creative problem solving, and the use of state-of-the-art technologies. In collaboration with the Gene Therapy Acceleration Unit (GTx), we aim to develop and implement assays to study various aspects of gene therapy and therapeutic candidates in vitro. This individual will contribute to key projects through the application of mammalian cell culture, semi-automated liquid handling, data handling and data analysis. Additional responsibilities include robust documentation of experiments in an electronic notebook, working with assay scientists and automation engineers to increase instrument performance, and execute screens through the use of cell types relevant to neurology. The candidate is expected to design scientific experiments and perform comprehensive data analysis using specialized software to process HTS and dose response data (e.g. TIBCO Spotfire, Genedata Screener).   qualifications: Legal authorization to work in the U.S.This position requires a Bachelor's degree in Biology or a related discipline and experience with HTS instruments to support drug discoveryDemonstrated broad expertise in various assay methodologies including high content analysis (confocal microscopy), standard plate reader compatible assays including protein-protein interaction readouts (e.g. FRET/BRET, AlphaLISA, MSD).Familiarity with Hamilton and Biomek workstations, Labcyte Echo, HighRes systems and various fluid handlers is preferredThe successful candidate will be highly motivated with a demonstrated ability to successfully take on challenges, troubleshoot efficiently and quickly adapt to new responsibilitiesThe candidate must have excellent organization, oral and written communication skillsThe ability to collaborate and work effectively as part of a team is essential  skills: Assay Development, In Vitro, Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $30.00 - 34.60 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The company is seeking a highly motivated biologist to join the Bioassays & HTS team in support of Gene Therapy projects within the Biotherapeutic & Medicinal Sciences department. Our group develops small format assays, executes high throughput screens (HTS) and the subsequent assessment of candidate molecules as part of a collaborative team of scientists. The primary responsibilities for this position are development and implementation of innovative cell-based assays using high throughput technologies, use of data analysis tools to assess biological activity and advance portfolio projects. The candidate must have experience with in vitro cell culture, use of primary cells plus experience with a preference for experience in neurobiology. The successful candidate will accomplish our mission through innovation, open communication, teamwork, creative problem solving, and the use of state-of-the-art technologies. In collaboration with the Gene Therapy Acceleration Unit (GTx), we aim to develop and implement assays to study various aspects of gene therapy and therapeutic candidates in vitro. This individual will contribute to key projects through the application of mammalian cell culture, semi-automated liquid handling, data handling and data analysis. Additional responsibilities include robust documentation of experiments in an electronic notebook, working with assay scientists and automation engineers to increase instrument performance, and execute screens through the use of cell types relevant to neurology. The candidate is expected to design scientific experiments and perform comprehensive data analysis using specialized software to process HTS and dose response data (e.g. TIBCO Spotfire, Genedata Screener).   qualifications: Legal authorization to work in the U.S.This position requires a Bachelor's degree in Biology or a related discipline and experience with HTS instruments to support drug discoveryDemonstrated broad expertise in various assay methodologies including high content analysis (confocal microscopy), standard plate reader compatible assays including protein-protein interaction readouts (e.g. FRET/BRET, AlphaLISA, MSD).Familiarity with Hamilton and Biomek workstations, Labcyte Echo, HighRes systems and various fluid handlers is preferredThe successful candidate will be highly motivated with a demonstrated ability to successfully take on challenges, troubleshoot efficiently and quickly adapt to new responsibilitiesThe candidate must have excellent organization, oral and written communication skillsThe ability to collaborate and work effectively as part of a team is essential  skills: Assay Development, In Vitro, Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north billerica, massachusetts
    • permanent
    • $52,000 - $78,000 per year
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment.   location: North Billerica, Massachusetts job type: Permanent salary: $52,000 - 78,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: The Quality Management System Technical Specialist supports the company's Quality Systems processes, both paper and within the electronic Quality Management System. This individual supports the maintenance and enhancement of existing processes (change control, quality events, controlled documentation, records management, training, and others) and the implementation of new systems and processes. Support the electronic Quality Management System (CATSWeb QMS) and its users as a business-level superuser / administrator. Train users / develop training material, help users find information in the system, trouble-shoot process issues, and participate in implementation of updates and enhancements to Quality Systems processes; including change control, CAPA, deviations, complaints, document management, and training.Propose and implement improvements to Quality Systems business processes, to increase efficiency, enhance compliance and reduce system maintenance requirements.Provide project and validation support for all activities involving modifications, upgrades and or business process changes related to Quality Systems applications. Author validation documentation and execute validation activities in accordance with company and industry standards.Participate in the design and implementation of new or updated processes. Collaborate with end users to document user and functional requirements for new implementations or upgrades to processes and systems. May act as a business lead for small to medium size projects.Partner with the IT organization and vendors to resolve issues and manage initiatives related to the Quality Management System.Work as a team player across many functions, departments, and groups, acting as a technical / quality management system resource.Support regulatory agency inspections as a Subject Matter Expert and by participating in back room processes, such as information retrieval.Actively promotes safety rules and awareness. Demonstrates good safety practices at all times including the appropriate use of protective equipment. Reports and takes initiative to correct safety & environmental hazards.Actively demonstrates the company values.  qualifications: BS/BA degree in a scientific or technical field, with a minimum of 5 years experience in a GxP environment.Experience with electronic Quality Management Systems at the technical support level is highly desirable. Experience with the support of CATSWeb QMS is a plus.A combination of education, training and experience may be considered in lieu of the above stated qualifications.Must have excellent written, verbal, and presentation skills. Must be able to interact effectively with all levels of management.Excellent organizational, analytical, and problem-solving skills and strong attention to detail.  skills: Quality Assurance, CAPA Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a conditi