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6 jobs found in new york

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    • brooklyn, new york
    • permanent
    • $110,000 - $111,000 per year
    job summary: Job Description Product Development Engineer This is a newly created position reflecting the growth and opportunities facing the company. This position will be a key member of the R&D/Product Development team. This position will be also critical in the transfer of technology and subsequent iterations from and to manufacturing. Compensation will be competitive including equity participation for the right candidate.   location: Brooklyn, New York job type: Permanent salary: $110,000 - 111,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Responsibilities : Plan and rapidly manage/implement new product transition activities between proof-of-concept and manufacturing/commercializationDrive the implementation and fulfillment of design control requirements related to development of medical devices.Create development documentation consistent with design control requirements such as product specifications, verification/validations studies, etc.Design and conduct experimentsDocument testing and experimental work in accordance with GLP/GMP. Coordinate with outside labs, suppliers, regulatory bodies supporting product development, product testing and process developmentConduct performance testing to assist research programs and development projectsManage and conduct the translation of customer needs into product requirements and design specifications.Participate in early-stage development, prototyping, and test activitiesAcquire and maintain relevant technical expertise in relevant fields: polymer science, protein chemistry, and biomaterials.Mentor other team members and work closely with other researcher and development team.Develop original ideas to advance the execution of the company's research and development objectives (we are looking for someone who can execute the R&D plans developed by the company as well as provide original thinking to shape the ongoing formulation of those plans)   qualifications: The right candidate will possess some or all of the following academic credentials, skills and experience: BSc or MSC in Materials Science and Engineering, Polymer Science (experience in biomaterials) or related field, with 3+ of experience in medical device product development.Proven success in product development in the medical device industry.Demonstrated ability to multi-task and to function in a fast-paced start-up environment, manage time efficiently, achieve goals with minimal supervision and effectively interact with other employees, departments, service providers and development partnersExperience in design controls, biocompatibility (ISO 10993), safety (ISO 22442) and toxicity requirements for medical device regulatory approvals.Independent experimental design capabilityCapability to develop custom assays.Expertise in fabrication and testing of hydrogels and/or protein-based materials - preferred.Experience with CAD modeling software (e.g. SolidWorks) and 3D printing methods- preferred.Ability to mentor researchers and lead a research project independentlyExceptional attention to detail and organizational skillsGoal oriented, motivated, and ability to work independentlyExcellent communication skills and comfortable working in a fast-paced environmentWillingness to learn and develop expert proficiency in new skills and applications relevant to your role as directed by the CSO Job Type: Full-time   skills: Medical Device Product Development 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: Job Description Product Development Engineer This is a newly created position reflecting the growth and opportunities facing the company. This position will be a key member of the R&D/Product Development team. This position will be also critical in the transfer of technology and subsequent iterations from and to manufacturing. Compensation will be competitive including equity participation for the right candidate.   location: Brooklyn, New York job type: Permanent salary: $110,000 - 111,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Responsibilities : Plan and rapidly manage/implement new product transition activities between proof-of-concept and manufacturing/commercializationDrive the implementation and fulfillment of design control requirements related to development of medical devices.Create development documentation consistent with design control requirements such as product specifications, verification/validations studies, etc.Design and conduct experimentsDocument testing and experimental work in accordance with GLP/GMP. Coordinate with outside labs, suppliers, regulatory bodies supporting product development, product testing and process developmentConduct performance testing to assist research programs and development projectsManage and conduct the translation of customer needs into product requirements and design specifications.Participate in early-stage development, prototyping, and test activitiesAcquire and maintain relevant technical expertise in relevant fields: polymer science, protein chemistry, and biomaterials.Mentor other team members and work closely with other researcher and development team.Develop original ideas to advance the execution of the company's research and development objectives (we are looking for someone who can execute the R&D plans developed by the company as well as provide original thinking to shape the ongoing formulation of those plans)   qualifications: The right candidate will possess some or all of the following academic credentials, skills and experience: BSc or MSC in Materials Science and Engineering, Polymer Science (experience in biomaterials) or related field, with 3+ of experience in medical device product development.Proven success in product development in the medical device industry.Demonstrated ability to multi-task and to function in a fast-paced start-up environment, manage time efficiently, achieve goals with minimal supervision and effectively interact with other employees, departments, service providers and development partnersExperience in design controls, biocompatibility (ISO 10993), safety (ISO 22442) and toxicity requirements for medical device regulatory approvals.Independent experimental design capabilityCapability to develop custom assays.Expertise in fabrication and testing of hydrogels and/or protein-based materials - preferred.Experience with CAD modeling software (e.g. SolidWorks) and 3D printing methods- preferred.Ability to mentor researchers and lead a research project independentlyExceptional attention to detail and organizational skillsGoal oriented, motivated, and ability to work independentlyExcellent communication skills and comfortable working in a fast-paced environmentWillingness to learn and develop expert proficiency in new skills and applications relevant to your role as directed by the CSO Job Type: Full-time   skills: Medical Device Product Development 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.
    • old bethpage, new york
    • temp to perm
    • $22.50 - $23 per hour
    job summary: About Our Client Our client provides innovative biomaterial solutions to orthopedic and dental customers around the world. Nearly 30 years of operation, our client has become a global leader in calcium phosphate-based biomaterial production and has developed proprietary plasma spray coatings and surface treatments. Our client also serves as a contract research facility, providing analytical services and materials testing in our customized biomaterial laboratories. Our state-of-the art 25,000 sq. ft. facility is located in Old Bethpage, New York.   location: Old Bethpage, New York job type: Temporary salary: $22.50 - 23.00 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Position Overview The biomaterials lab technician leads in carrying out experiments of research, development, and pilot production projects according to directed procedures. The biomaterials lab technician is also responsible for operating analytical equipment within the laboratory and keeping records of all procedures and analyses and maintaining good lab practices.   qualifications: Position Responsibilities ? Carefully and accurately carry out experiments to support research projects and new product development ? Work with the product development team to organize daily laboratory operations ? Assist product development team in creating and implementing protocols for new product developments and pre-existing product improvements, including co-design of research and development experiments ? Ensure laboratory compliance with established policies and procedures ? Analyze data and present updates to the product development team as well as other departments ? Be organized and proficient with all analytical and data processing equipment of the company ? Work safely in the lab, following lab safety guidelines ? Maintain careful and comprehensive records of all developments for the company's intellectual intelligence database, in accordance with ISO 13485:2016 ? Maintain raw material and finished product inventory ? Maintain the quality of the laboratory and its equipment ? Support and effectively interact with quality assurance personnel and engineers to help solve technical problems as appropriate ? Additional responsibilities as assigned by the Biomaterials Research Scientist   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: About Our Client Our client provides innovative biomaterial solutions to orthopedic and dental customers around the world. Nearly 30 years of operation, our client has become a global leader in calcium phosphate-based biomaterial production and has developed proprietary plasma spray coatings and surface treatments. Our client also serves as a contract research facility, providing analytical services and materials testing in our customized biomaterial laboratories. Our state-of-the art 25,000 sq. ft. facility is located in Old Bethpage, New York.   location: Old Bethpage, New York job type: Temporary salary: $22.50 - 23.00 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Position Overview The biomaterials lab technician leads in carrying out experiments of research, development, and pilot production projects according to directed procedures. The biomaterials lab technician is also responsible for operating analytical equipment within the laboratory and keeping records of all procedures and analyses and maintaining good lab practices.   qualifications: Position Responsibilities ? Carefully and accurately carry out experiments to support research projects and new product development ? Work with the product development team to organize daily laboratory operations ? Assist product development team in creating and implementing protocols for new product developments and pre-existing product improvements, including co-design of research and development experiments ? Ensure laboratory compliance with established policies and procedures ? Analyze data and present updates to the product development team as well as other departments ? Be organized and proficient with all analytical and data processing equipment of the company ? Work safely in the lab, following lab safety guidelines ? Maintain careful and comprehensive records of all developments for the company's intellectual intelligence database, in accordance with ISO 13485:2016 ? Maintain raw material and finished product inventory ? Maintain the quality of the laboratory and its equipment ? Support and effectively interact with quality assurance personnel and engineers to help solve technical problems as appropriate ? Additional responsibilities as assigned by the Biomaterials Research Scientist   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.
    • tarrytown, new york (remote)
    • contract
    • $80 - $90 per hour
    job summary: Job description: As a Statistical Programmer in Medical Analytics you will be responsible for programming aspects and deliverables for product(s)/project(s) with regards to our Medical Affairs activities. Together with Medical Analytics (Biostatistics), Medical Affairs and HEOR colleagues, you will plan and implement statistical analysis, provide input into and align with our publication plans, and support analysis needs. You will need to understand research questions, implement complex statistical analyses, and explain analysis implementations.   location: Tarrytown, New York job type: Contract salary: $80 - 90 per hour work hours: 9 to 5 education: Masters   responsibilities: A typical day may include the following: - Planning and executing Statistical Analysis - Authoring parts of and/or provide significant input into the Statistical Analysis Plan (SAP) to comprehensively and unambiguously define specifications, data derivations, and display shells to be generated in collaboration with key partners. - Performing statistical analyses using SAS to generate tables, listings, and figures for use in publications/presentations and for internal purposes. - Ensuring quality of deliverables through appropriate testing/validation and active review for completeness and accuracy (including developing and implementing a well-documented validation plan). - Understanding ICH, GCP and health authority guidelines with regard to reporting and associated regulations and standards (including CDISC standards). This may be for you if you: - Have the ability to explain/discuss implementation details of complex statistical analyses to both technical and non-technical audiences - Enjoy working with a cross functional team - Can work in a fast paced, rapid-response environment   qualifications: To be considered for this you need a MS or PhD in statistics, biostatistics, mathematics, engineering, computer science, life sciences or related subject area. Your experience should include 3+ years of experience in statistical programming using SAS in the biotechnology, pharmaceutical or health related industries. Your statistical programming method experience would ideally have supported: - Medical Affairs including analysis using the clinical database for scientific meetings, publications, and internal decision-making (generally based on previously conducted randomized clinical trials). - Health Economics and Outcomes Research including analysis related to patient reported outcomes (including development/validation) and HTA/reimbursement/value dossiers. Additional experiences would include: - Proficiency in SAS/STAT modules that support linear models, categorical data, and time-to-event data. - Familiarity with SAS high-resolution graphics to supplement aforementioned statistical models. - Ability to make use of standard macros or author specialized limited-use macros. - Experience with R including RShiny and RMarkdown while not required are a plus.   skills: ADaM, CDISC 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: Job description: As a Statistical Programmer in Medical Analytics you will be responsible for programming aspects and deliverables for product(s)/project(s) with regards to our Medical Affairs activities. Together with Medical Analytics (Biostatistics), Medical Affairs and HEOR colleagues, you will plan and implement statistical analysis, provide input into and align with our publication plans, and support analysis needs. You will need to understand research questions, implement complex statistical analyses, and explain analysis implementations.   location: Tarrytown, New York job type: Contract salary: $80 - 90 per hour work hours: 9 to 5 education: Masters   responsibilities: A typical day may include the following: - Planning and executing Statistical Analysis - Authoring parts of and/or provide significant input into the Statistical Analysis Plan (SAP) to comprehensively and unambiguously define specifications, data derivations, and display shells to be generated in collaboration with key partners. - Performing statistical analyses using SAS to generate tables, listings, and figures for use in publications/presentations and for internal purposes. - Ensuring quality of deliverables through appropriate testing/validation and active review for completeness and accuracy (including developing and implementing a well-documented validation plan). - Understanding ICH, GCP and health authority guidelines with regard to reporting and associated regulations and standards (including CDISC standards). This may be for you if you: - Have the ability to explain/discuss implementation details of complex statistical analyses to both technical and non-technical audiences - Enjoy working with a cross functional team - Can work in a fast paced, rapid-response environment   qualifications: To be considered for this you need a MS or PhD in statistics, biostatistics, mathematics, engineering, computer science, life sciences or related subject area. Your experience should include 3+ years of experience in statistical programming using SAS in the biotechnology, pharmaceutical or health related industries. Your statistical programming method experience would ideally have supported: - Medical Affairs including analysis using the clinical database for scientific meetings, publications, and internal decision-making (generally based on previously conducted randomized clinical trials). - Health Economics and Outcomes Research including analysis related to patient reported outcomes (including development/validation) and HTA/reimbursement/value dossiers. Additional experiences would include: - Proficiency in SAS/STAT modules that support linear models, categorical data, and time-to-event data. - Familiarity with SAS high-resolution graphics to supplement aforementioned statistical models. - Ability to make use of standard macros or author specialized limited-use macros. - Experience with R including RShiny and RMarkdown while not required are a plus.   skills: ADaM, CDISC 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.
    • aquebogue, new york
    • permanent
    • $60,000 - $70,000 per year
    job summary: Job Description: Immediate openings for Quality Assurance Specialists at established sterile pharmaceutical manufacturer. Preferred Candidates have an BS or equivalent in Pharma, RA and/or Chemistry, Biochemistry, or Microbiology. All candidates must possess strong organizational and writing skills; ability to multitask; and proficiency in Word, Excel, and Adobe. QA Professionals with experience in the pharmaceutical industry, or other industries that employ advanced Quality Management Systems, are preferred. Will also consider trainee candidates with the requisite educational background. Salary commensurate with experience.   location: Aquebogue, New York job type: Permanent salary: $60,000 - 70,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: Responsibilities may include: Batch record review, in-process inspections, submitting and managing test samples, performing investigations, preparing and implementing remediation and CAPA plans across multiple disciplines (manufacturing, chemistry, microbiology, maintenance and quality); performing CAPA effectiveness checks; preparing/revising and implementing SOPs; training staff; tracking and trending data; and supporting facility/systems upgrade projects.   qualifications: Privately held company with CEO with decades of experience and knowledge. Managers and key employees have been with us for 10 years or more - we are looking for people to be part of the team long term. Great opportunities for career growth. COVID-19 considerations: all personnel are temperature monitored daily prior to entry; must wear masks when away from their desks; facility is sanitized several times daily.   skills: Microbiology 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: Job Description: Immediate openings for Quality Assurance Specialists at established sterile pharmaceutical manufacturer. Preferred Candidates have an BS or equivalent in Pharma, RA and/or Chemistry, Biochemistry, or Microbiology. All candidates must possess strong organizational and writing skills; ability to multitask; and proficiency in Word, Excel, and Adobe. QA Professionals with experience in the pharmaceutical industry, or other industries that employ advanced Quality Management Systems, are preferred. Will also consider trainee candidates with the requisite educational background. Salary commensurate with experience.   location: Aquebogue, New York job type: Permanent salary: $60,000 - 70,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: Responsibilities may include: Batch record review, in-process inspections, submitting and managing test samples, performing investigations, preparing and implementing remediation and CAPA plans across multiple disciplines (manufacturing, chemistry, microbiology, maintenance and quality); performing CAPA effectiveness checks; preparing/revising and implementing SOPs; training staff; tracking and trending data; and supporting facility/systems upgrade projects.   qualifications: Privately held company with CEO with decades of experience and knowledge. Managers and key employees have been with us for 10 years or more - we are looking for people to be part of the team long term. Great opportunities for career growth. COVID-19 considerations: all personnel are temperature monitored daily prior to entry; must wear masks when away from their desks; facility is sanitized several times daily.   skills: Microbiology 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.
    • aquebogue, new york
    • permanent
    • $70,000 - $85,000 per year
    job summary: Job Description: Immediate openings at established sterile pharmaceutical manufacturer for Quality Control Analysts in our Microbiology Laboratories. Requirements: BS degree in in Biology, Biochemistry, Microbiology or Chemistry (or equivalent). Preferred candidates possess experience in the pharmaceutical industry, in a sterile manufacturing facility. Salary commensurate with experience. Excellent facilities located in Riverhead, NY Privately held company with CEO with decades of experience and knowledge. Managers and key employees have been with us for 10 years or more - we are looking for people to be part of the team long term. Great opportunities for career growth. COVID-19 considerations: all personnel are temperature monitored daily prior to entry; must wear masks when away from their desks; facility is sanitized several times daily.   location: Aquebogue, New York job type: Permanent salary: $70,000 - 85,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: Responsibilities may include USP and In-House Testing of raw materials, components, water and finished products.Perform Environmental and Personnel Monitoring of the sterile production facility.Testing in support of qualification of the sterile production facility and equipment in compliance with FDA requirements.Qualification in Gowning and Aseptic Techniques  qualifications: Privately held company with CEO with decades of experience and knowledge. Managers and key employees have been with us for 10 years or more - we are looking for people to be part of the team long term. Great opportunities for career growth. COVID-19 considerations: all personnel are temperature monitored daily prior to entry; must wear masks when away from their desks; facility is sanitized several times daily.   skills: Microbiology 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: Job Description: Immediate openings at established sterile pharmaceutical manufacturer for Quality Control Analysts in our Microbiology Laboratories. Requirements: BS degree in in Biology, Biochemistry, Microbiology or Chemistry (or equivalent). Preferred candidates possess experience in the pharmaceutical industry, in a sterile manufacturing facility. Salary commensurate with experience. Excellent facilities located in Riverhead, NY Privately held company with CEO with decades of experience and knowledge. Managers and key employees have been with us for 10 years or more - we are looking for people to be part of the team long term. Great opportunities for career growth. COVID-19 considerations: all personnel are temperature monitored daily prior to entry; must wear masks when away from their desks; facility is sanitized several times daily.   location: Aquebogue, New York job type: Permanent salary: $70,000 - 85,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: Responsibilities may include USP and In-House Testing of raw materials, components, water and finished products.Perform Environmental and Personnel Monitoring of the sterile production facility.Testing in support of qualification of the sterile production facility and equipment in compliance with FDA requirements.Qualification in Gowning and Aseptic Techniques  qualifications: Privately held company with CEO with decades of experience and knowledge. Managers and key employees have been with us for 10 years or more - we are looking for people to be part of the team long term. Great opportunities for career growth. COVID-19 considerations: all personnel are temperature monitored daily prior to entry; must wear masks when away from their desks; facility is sanitized several times daily.   skills: Microbiology 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.
    • grand island, new york
    • contract
    • $15 - $17.95 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. 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: Grand Island, New York job type: Contract salary: $15.00 - 17.95 per hour work hours: 9 to 5 education: Bachelors   responsibilities: This position serves in the capacity of performing general laboratory tasks of testing finished products, stability, raw material, utilities, and monitoring for environmental control, as well as supporting validations of rooms, equipment and materials.This position reports to the supervisor for the functional area to which they are assigned and has no direct reports.The QC Technician II position works closely with other departments, such as validations, chemistry, Operations, Product Development, Quality Systems and Product Release to assure the support of the Microbiology department on various projects, studies and routine tasks.This individual holding the position of QC Technician II shall be responsible for performing routine testing of in-process and finished product samples, raw material, stability, and utilities.They shall be responsible for monitoring the environmental conditions in the laboratory and in manufacturing areas.They shall support validation projects.  qualifications: Bachelors in a science field preferably biology based   skills: Quality control, GLP (Good Laboratory Practice), 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. 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: Grand Island, New York job type: Contract salary: $15.00 - 17.95 per hour work hours: 9 to 5 education: Bachelors   responsibilities: This position serves in the capacity of performing general laboratory tasks of testing finished products, stability, raw material, utilities, and monitoring for environmental control, as well as supporting validations of rooms, equipment and materials.This position reports to the supervisor for the functional area to which they are assigned and has no direct reports.The QC Technician II position works closely with other departments, such as validations, chemistry, Operations, Product Development, Quality Systems and Product Release to assure the support of the Microbiology department on various projects, studies and routine tasks.This individual holding the position of QC Technician II shall be responsible for performing routine testing of in-process and finished product samples, raw material, stability, and utilities.They shall be responsible for monitoring the environmental conditions in the laboratory and in manufacturing areas.They shall support validation projects.  qualifications: Bachelors in a science field preferably biology based   skills: Quality control, GLP (Good Laboratory Practice), 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.

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