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10 jobs found in north carolina

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    • research triangle park, north carolina
    • contract
    • $27.37 - $32.20 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: Durham, North Carolina job type: Contract salary: $27.37 - 32.20 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Performs release and stability testing and all associated activities associated with this testing.Technical leadership as a subject matter expert in one or more disciplines.Execution of method transfer, method/reagent qualification, analytical improvement projects, and validation of analytical methods in collaboration with teams as appropriate.Supports maintenance of effective laboratory systems to ensure integrity of all laboratory results.Adherence to all GMP requirements, effective interactions/communication with Quality Control management and support of investigations.  qualifications: Biological Science degree is preferred with 0-2 years (M.S. or B.S.) of relevant experience in a GMP lab role.Candidates should have experience with biological testing (bioassays, cell-based or not), ELISAs, potency and binding assays and extensive GMP experience, preferably in a commercial manufacturing environment.Excellent laboratory technique and experimental design.Experience with statistical experimental design and data analysis with JMP and Excel software, as well as relevant experience in reagent qualification, method validation and transfer is a plus.Excellent time management and prioritization skills.Excellent oral and written communication and presentation skills  skills: Quality control, Assay Verification, 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. 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: Durham, North Carolina job type: Contract salary: $27.37 - 32.20 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Performs release and stability testing and all associated activities associated with this testing.Technical leadership as a subject matter expert in one or more disciplines.Execution of method transfer, method/reagent qualification, analytical improvement projects, and validation of analytical methods in collaboration with teams as appropriate.Supports maintenance of effective laboratory systems to ensure integrity of all laboratory results.Adherence to all GMP requirements, effective interactions/communication with Quality Control management and support of investigations.  qualifications: Biological Science degree is preferred with 0-2 years (M.S. or B.S.) of relevant experience in a GMP lab role.Candidates should have experience with biological testing (bioassays, cell-based or not), ELISAs, potency and binding assays and extensive GMP experience, preferably in a commercial manufacturing environment.Excellent laboratory technique and experimental design.Experience with statistical experimental design and data analysis with JMP and Excel software, as well as relevant experience in reagent qualification, method validation and transfer is a plus.Excellent time management and prioritization skills.Excellent oral and written communication and presentation skills  skills: Quality control, Assay Verification, 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.
    • raleigh, north carolina
    • permanent
    • $40,000 - $45,000 per year
    job summary: The successful candidate will assist Business Development Team in all aspects of sales for Scientific Consulting, Accounting, and Grants Management services. The Sales Associate will train under experienced Business Development professionals and will gain experience in inside and outside sales; Salesforce; other sales activities.   location: Raleigh, North Carolina job type: Permanent salary: $40,000 - 45,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Maintain Salesforce CRM.Serve as contact for press inquiries and press releases alongside BD Manager.Participate in prospective client calls and meetings. Attend conferences as needed.Prepare follow-up emails and other correspondence for prospective clients.Develop and release company newsletters in support of Marketing Associate as needed.Coordinate closely with all departments to support their sales & marketing needs.Stays abreast of competitors and sales trends.Excellent sales service to ensure high levels of customer satisfaction.Follow and achieve department's sales goals on a monthly, quarterly and yearly basis  qualifications: Bachelor's degree in Sales, Marketing, or similar field. A science degree with a desire to enter a career in Sales/Marketing is also acceptable.Understanding of basic sales and marketing principles.Ability to create sales and marketing materials.Passion for helping companies and entrepreneurs advance their scientific discoveries.Ability to learn new tasks quickly and adapt accordingly.Ability to work independently and efficiently in a dynamic, growing entrepreneurial environment.Exceptional organization skills.Detail-oriented.Ability to meet deadlines.Strong communication skills, both written and verbal.Ability to work well independently and in teams.  skills: Sales Training 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: The successful candidate will assist Business Development Team in all aspects of sales for Scientific Consulting, Accounting, and Grants Management services. The Sales Associate will train under experienced Business Development professionals and will gain experience in inside and outside sales; Salesforce; other sales activities.   location: Raleigh, North Carolina job type: Permanent salary: $40,000 - 45,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Maintain Salesforce CRM.Serve as contact for press inquiries and press releases alongside BD Manager.Participate in prospective client calls and meetings. Attend conferences as needed.Prepare follow-up emails and other correspondence for prospective clients.Develop and release company newsletters in support of Marketing Associate as needed.Coordinate closely with all departments to support their sales & marketing needs.Stays abreast of competitors and sales trends.Excellent sales service to ensure high levels of customer satisfaction.Follow and achieve department's sales goals on a monthly, quarterly and yearly basis  qualifications: Bachelor's degree in Sales, Marketing, or similar field. A science degree with a desire to enter a career in Sales/Marketing is also acceptable.Understanding of basic sales and marketing principles.Ability to create sales and marketing materials.Passion for helping companies and entrepreneurs advance their scientific discoveries.Ability to learn new tasks quickly and adapt accordingly.Ability to work independently and efficiently in a dynamic, growing entrepreneurial environment.Exceptional organization skills.Detail-oriented.Ability to meet deadlines.Strong communication skills, both written and verbal.Ability to work well independently and in teams.  skills: Sales Training 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.
    • morrisville, north carolina
    • contract
    • $28 - $32.20 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: Morrisville, North Carolina job type: Contract salary: $28.00 - 32.20 per hour work hours: 9 to 5 education: No Degree Required   responsibilities: The Quality Control Raw Materials Associate I is responsible for contributing to key functional, tactical, strategic and operational aspects of the Quality Control Raw Materials group at the Company's RTP site.The Raw Material Associate I's responsibilities include, but are not limited to release testing of raw materials using compendia (USP, Ph. Eur, and JP/JPE) and analytical methods, as well as validation/transfer of analytical methods, and technical support of QC investigations.Additional responsibilities include entering data into electronic laboratory information management system and inventory control systems, and completing all training/course requirements while maintaining 100% compliance on all assignments.  qualifications: This position interfaces with QC Chemistry, Quality, Planning, Warehouse, and Manufacturing customers.The Associate I may also support the Supervisor/Manager for activities related to compliance with GMP, and identifying corrective actions on the floor.The Associate I should be able to work effectively both independently and within a team framework, requiring both robust written and verbal communication skills.  skills: Quality control, Chemistry, 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. 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: Morrisville, North Carolina job type: Contract salary: $28.00 - 32.20 per hour work hours: 9 to 5 education: No Degree Required   responsibilities: The Quality Control Raw Materials Associate I is responsible for contributing to key functional, tactical, strategic and operational aspects of the Quality Control Raw Materials group at the Company's RTP site.The Raw Material Associate I's responsibilities include, but are not limited to release testing of raw materials using compendia (USP, Ph. Eur, and JP/JPE) and analytical methods, as well as validation/transfer of analytical methods, and technical support of QC investigations.Additional responsibilities include entering data into electronic laboratory information management system and inventory control systems, and completing all training/course requirements while maintaining 100% compliance on all assignments.  qualifications: This position interfaces with QC Chemistry, Quality, Planning, Warehouse, and Manufacturing customers.The Associate I may also support the Supervisor/Manager for activities related to compliance with GMP, and identifying corrective actions on the floor.The Associate I should be able to work effectively both independently and within a team framework, requiring both robust written and verbal communication skills.  skills: Quality control, Chemistry, 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.
    • research triangle park, north carolina (remote)
    • contract
    • $32.48 - $38.22 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: Durham, North Carolina job type: Contract salary: $32.48 - 38.22 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Senior Quality Assurance Associate is responsible for contributing to the oversight of key strategic, tactical, and operational aspects within Quality Assurance. Activities include, but are not limited to: review of GMP raw data for compliance, review of GMP documentation to support batch disposition, review/approval of GMP procedures, protocols and reports, GxP Quality systems-related training, identify gaps in existing Quality systems and propose solutions to site management. Review and approval of batch related documentation (cGMP procedures, Master Production Records, Solution Lot records, protocols and reports) to support product dispositionReview of executed Batch Records, procedures, forms, master production recordsReview and approval of InvestigationsExecutes activities including; intermediate technical writing, intermediate investigation support (root cause analysis/impact assessment), project representation (moderate complexity)Supports resolution of both technical and compliance issues/gaps of moderate complexity. Aides in implementation of Quality Systems/System Improvements with some guidance, moderate technical problem solving (tools or enterprise systems) within function and across multiple functional areasAssists Quality Assurance Management in additional responsibilities related to the day-to-day implementation of the Quality Management Systems required to maintain cGMP compliance, and ensure the safety, efficacy and purity of the products manufactured by the companyControl and release of equipment from maintenance, validation, change control and product changeoverSupports and/or assists in GxP quality systems-related training. Provides some mentorship and training within and across functions  qualifications: Quality and Compliance experience (CFR, ICH, ISO, etc.)Biologics experience (Cell Culture and Purification Manufacturing experience)Experience with Trackwise and/or ORACLE/SAP  skills: Quality Assurance, Protein Purification, Cell Cultures, 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. 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: Durham, North Carolina job type: Contract salary: $32.48 - 38.22 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Senior Quality Assurance Associate is responsible for contributing to the oversight of key strategic, tactical, and operational aspects within Quality Assurance. Activities include, but are not limited to: review of GMP raw data for compliance, review of GMP documentation to support batch disposition, review/approval of GMP procedures, protocols and reports, GxP Quality systems-related training, identify gaps in existing Quality systems and propose solutions to site management. Review and approval of batch related documentation (cGMP procedures, Master Production Records, Solution Lot records, protocols and reports) to support product dispositionReview of executed Batch Records, procedures, forms, master production recordsReview and approval of InvestigationsExecutes activities including; intermediate technical writing, intermediate investigation support (root cause analysis/impact assessment), project representation (moderate complexity)Supports resolution of both technical and compliance issues/gaps of moderate complexity. Aides in implementation of Quality Systems/System Improvements with some guidance, moderate technical problem solving (tools or enterprise systems) within function and across multiple functional areasAssists Quality Assurance Management in additional responsibilities related to the day-to-day implementation of the Quality Management Systems required to maintain cGMP compliance, and ensure the safety, efficacy and purity of the products manufactured by the companyControl and release of equipment from maintenance, validation, change control and product changeoverSupports and/or assists in GxP quality systems-related training. Provides some mentorship and training within and across functions  qualifications: Quality and Compliance experience (CFR, ICH, ISO, etc.)Biologics experience (Cell Culture and Purification Manufacturing experience)Experience with Trackwise and/or ORACLE/SAP  skills: Quality Assurance, Protein Purification, Cell Cultures, 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.
    • durham, north carolina
    • contract
    • $22.10 - $26 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: Durham, North Carolina job type: Contract salary: $22.10 - 26.00 per hour work hours: 9 to 5 education: Associate   responsibilities: Summary: The main function of a lab technician is to perform routine medical laboratory tests for the diagnosis, treatment and prevention of disease. A typical lab technician may work under the supervision of a medical technologist. Job Responsibilities: Set up, adjust, maintain and clean medical laboratory equipment.Analyze the results of tests and experiments to ensure conformity to specifications, using special mechanical and electrical devices.Analyze, gather and record test data to issue reports that use charts, graphs and narratives.Obtain specimens, cultivating, isolating and identifying microorganisms for analysis.May examine cells stained with dye to locate abnormalities.Consult with a pathologist to determine a final diagnosis when abnormal cells are found.   qualifications: Skills: Verbal and written communication skills, attention to detail, and problem solving skills.Basic ability to work independently and manage ones time.Basic knowledge of the information and techniques needed to diagnose and treat human injuries and diseases.Basic ability to analyze data and accurately document and record results. Education/Experience: High school diploma or GED required.Associate's degree in medical technology or vocational training preferred.  skills: GLP (Good Laboratory 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. 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: Durham, North Carolina job type: Contract salary: $22.10 - 26.00 per hour work hours: 9 to 5 education: Associate   responsibilities: Summary: The main function of a lab technician is to perform routine medical laboratory tests for the diagnosis, treatment and prevention of disease. A typical lab technician may work under the supervision of a medical technologist. Job Responsibilities: Set up, adjust, maintain and clean medical laboratory equipment.Analyze the results of tests and experiments to ensure conformity to specifications, using special mechanical and electrical devices.Analyze, gather and record test data to issue reports that use charts, graphs and narratives.Obtain specimens, cultivating, isolating and identifying microorganisms for analysis.May examine cells stained with dye to locate abnormalities.Consult with a pathologist to determine a final diagnosis when abnormal cells are found.   qualifications: Skills: Verbal and written communication skills, attention to detail, and problem solving skills.Basic ability to work independently and manage ones time.Basic knowledge of the information and techniques needed to diagnose and treat human injuries and diseases.Basic ability to analyze data and accurately document and record results. Education/Experience: High school diploma or GED required.Associate's degree in medical technology or vocational training preferred.  skills: GLP (Good Laboratory 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.
    • durham, north carolina
    • temporary
    • $36 - $38 per hour
    Are you seeking a job that involves technical writing and investigative skills in a manufacturing environment? In this 12-month contract position, you will lead investigations for minor Quality deviations and incidents, focus on improvement and risk reduction, identify root causes and make recommendations to correct. Contribute to metrics related to investigation process and CAPA effectiveness.  If you have a 4-year degree, possess technical knowledge of manufacturing processes,investigating and writing, apply today!salary: $36 - $38 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilities• Responsibilities include the following: • Limited technical knowledge of Manufacturing equipment and processes – must demonstrate minor level of technical depth and process knowledge of Manufacturing operations • Authors and/or issues manufacturing documentation, including Batch Production Records, Solution Lot Records, Procedures, and Work Instructions to meet production schedule with high degree of supervision from key stakeholders and Management • Will support Manufacturing focused Change Controls, Corrective and Preventive Actions (CAPAs), and Planned Exceptions • Project Management and Project Execution – may participate in some small project(s) (minor in nature) and execute job tasks associated with the project • Partners with Manufacturing, Manufacturing Sciences, Engineering, Automation, Quality, Planning, and Materials Management to identify continuous improvement opportunitiesThe essential functions of this role include:working in a smoke free environmentwearing steel toe shoesSkillsInvestigationsManufacturingWriting - DocumentationQualificationsYears 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. 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.
    Are you seeking a job that involves technical writing and investigative skills in a manufacturing environment? In this 12-month contract position, you will lead investigations for minor Quality deviations and incidents, focus on improvement and risk reduction, identify root causes and make recommendations to correct. Contribute to metrics related to investigation process and CAPA effectiveness.  If you have a 4-year degree, possess technical knowledge of manufacturing processes,investigating and writing, apply today!salary: $36 - $38 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilities• Responsibilities include the following: • Limited technical knowledge of Manufacturing equipment and processes – must demonstrate minor level of technical depth and process knowledge of Manufacturing operations • Authors and/or issues manufacturing documentation, including Batch Production Records, Solution Lot Records, Procedures, and Work Instructions to meet production schedule with high degree of supervision from key stakeholders and Management • Will support Manufacturing focused Change Controls, Corrective and Preventive Actions (CAPAs), and Planned Exceptions • Project Management and Project Execution – may participate in some small project(s) (minor in nature) and execute job tasks associated with the project • Partners with Manufacturing, Manufacturing Sciences, Engineering, Automation, Quality, Planning, and Materials Management to identify continuous improvement opportunitiesThe essential functions of this role include:working in a smoke free environmentwearing steel toe shoesSkillsInvestigationsManufacturingWriting - DocumentationQualificationsYears 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. 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.
    • durham, north carolina
    • contract
    • $23.84 - $28.05 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: Durham, North Carolina job type: Contract salary: $23.84 - 28.05 per hour work hours: 9 to 5 education: Associate   responsibilities: Under the supervision of the Microbiology Lab Supervisor, technician performs sample collection, microbiological and tissue culture tasks associated with new or modified products or processes, contamination control and sterilization operations. Supports the Quality Assurance Department by taking an active role in team sharing, problem solving tasks, team activities and team and plant-wide subgroups focusing on the plant goals of safety, quality, schedule and cost. Performs environmental monitoring (EM) for production areas, processes and personnel for evaluating microbial and particulate contamination using air samplers, settle plates, contact plates, and particle counters.Collects and tests product samples according to documented procedures.Maintains cell line cultures and microbial cultures.Duties may include cell harvesting, scheduling cell line maintenance, conducting routine media changes, reviving newly purchased cell, quantifying cell inoculum.Performs general laboratory tasks such as media preparation, autoclaving supplies, wash and prepare glassware, discard waste and cultures following appropriate practices.Performs / tracks routine preventive maintenance and monitoring of laboratory equipment and supplies.Maintains accurate and current records of all results and procedures.Must be able to ensure a high degree of accuracy in all tests results obtained.Complies with safety standards and Good Laboratory Practice standards.Interacts with production personnel to ensure product sample collection.  qualifications: Must have a minimum of a two-year Associate Degree with course work in chemistry and biology.Must Have (1) year experience in a microbiology laboratory technician or microbiology testing lab position.Requires good written and oral communication skills. Must be highly motivated, detail oriented, possess excellent organizational and problem-solving skills, and be effective as a team player.Must possess the ability to work independently and manage multiple priorities and multi-task projects.Must be an independent thinker, self-starter, and perform responsibilities under very limited supervision.Must have a working knowledge of spreadsheet applications and word processing to perform necessary tasks for preparing required correspondence, reports and communication.Must be flexible and be willing to work overtime as required.Prior experience with a high-performance work team system preferred.  skills: GLP (Good Laboratory Practice), Microbiology, 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. 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: Durham, North Carolina job type: Contract salary: $23.84 - 28.05 per hour work hours: 9 to 5 education: Associate   responsibilities: Under the supervision of the Microbiology Lab Supervisor, technician performs sample collection, microbiological and tissue culture tasks associated with new or modified products or processes, contamination control and sterilization operations. Supports the Quality Assurance Department by taking an active role in team sharing, problem solving tasks, team activities and team and plant-wide subgroups focusing on the plant goals of safety, quality, schedule and cost. Performs environmental monitoring (EM) for production areas, processes and personnel for evaluating microbial and particulate contamination using air samplers, settle plates, contact plates, and particle counters.Collects and tests product samples according to documented procedures.Maintains cell line cultures and microbial cultures.Duties may include cell harvesting, scheduling cell line maintenance, conducting routine media changes, reviving newly purchased cell, quantifying cell inoculum.Performs general laboratory tasks such as media preparation, autoclaving supplies, wash and prepare glassware, discard waste and cultures following appropriate practices.Performs / tracks routine preventive maintenance and monitoring of laboratory equipment and supplies.Maintains accurate and current records of all results and procedures.Must be able to ensure a high degree of accuracy in all tests results obtained.Complies with safety standards and Good Laboratory Practice standards.Interacts with production personnel to ensure product sample collection.  qualifications: Must have a minimum of a two-year Associate Degree with course work in chemistry and biology.Must Have (1) year experience in a microbiology laboratory technician or microbiology testing lab position.Requires good written and oral communication skills. Must be highly motivated, detail oriented, possess excellent organizational and problem-solving skills, and be effective as a team player.Must possess the ability to work independently and manage multiple priorities and multi-task projects.Must be an independent thinker, self-starter, and perform responsibilities under very limited supervision.Must have a working knowledge of spreadsheet applications and word processing to perform necessary tasks for preparing required correspondence, reports and communication.Must be flexible and be willing to work overtime as required.Prior experience with a high-performance work team system preferred.  skills: GLP (Good Laboratory Practice), Microbiology, 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.
    • greenville, north carolina
    • permanent
    • $70,000 - $80,000 per year
    job summary: This position performs routine and non-routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements. This role provides laboratory troubleshooting for a team to assist in the successful and timely execution of laboratory analyses.   location: Greenville, North Carolina job type: Permanent salary: $70,000 - 80,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Analytical Testing: With limited supervision, perform a broad array of primary and advanced analytical testing methods (wet and dry chemistry) in compliance with all cGMP and regulatory guidelines and ensure the highest standards for efficiency, right first-time measures, and quality standardsClient Service: Support and sometimes participate in the direct interaction with client organizations to assure timely and complete reporting, problem-solving and the highest level of service and responsivenessData Integrity: Ensure integrity of data through accurate transactions, documentation, and tracking of all cGMP activitiesData Interpretation and Problem-Solving: Use appropriate resources (e.g. software) toinvestigate and interpret data in support of recommendations for problem-solving related to methods, instruments and analytical techniques.Process Improvement: Identify and recommend opportunities for improved efficiencies, client service and teamwork within the analytical groupQuality: Ensure the quality of work, products and services as a first priority; comply with or exceed all regulatory and cGMP compliance standards as well as ensure accuracy of analyses as it relates to right first time measuresSafety: Adhere to all workplace safety laws, regulations, standards, and practices and actively advance a culture of safety within his or her team and organization.Independently perform routine and complex testing for chromatographic and spectrophotometric methods (HPLC, GC, UV) of analysis for excipients, new chemical entities and/or drug productsInterpret data and make recommendations to management for improvement or potential concernsCompare laboratory data against specifications, prepare reports, and trend data where applicable to determine if results meet requirementsEnsure proper usage, care, and return of calibration standards including, but not limited to, reference standards, timers, thermometers, and instrumentationEnsure accuracy of testing by following method/standard instructions and adhering to internal SOPs to eliminate the potential for repeat testing, deviations, and investigationsIndependently author standard operating procedures, analytical testing procedures, final submission ready documents, and create document templates for use by junior team membersCreate report templates and/or enter data into established reports/templates or software-based systemsReview routine laboratory experiments for accuracy and provide guidance to junior team members to ensure future complianceIdentify and recommend opportunities for improved efficiencies, internal/external client service and teamwork within the analytical groupServe as a point of contact for laboratory testing support and provide updates to laboratory supervision and/or clientWith supervision, support the scheduling and planning of internal/external client project work to ensure the highest levels of efficiency and quality standards are metSupport the development of a climate of quality within the teams by driving and monitoring quality standards within the teamBecome resident expert in the use of Empower (perform supervisory sign-off for electronic reports) and other software-based systemsServe as a method troubleshooting resource to identify and document critical factors that affect method performance and assist peers in resolving method issues in a timely, cost-effective mannerIndependently perform method evaluation/development/validation and troubleshooting instruments and improvement of processesAssist laboratory management with the preparation and execution of laboratory investigations/deviations and CAPA within the electronic quality system (eQMS)Mentor and train new laboratory team members  qualifications: Analytical Acumen: Skilled in the interpretation and application of data in problem-solving, decision-making, account planning, and activity prioritization.Decision Quality: Considers all relevant factors (analysis, wisdom, experience and judgment) and uses appropriate decision-making criteria and principles.Equipment Operation: Is skilled in the use and trouble-shooting of key equipment important in the delivery of the job.Problem Solving: Build a logical approach to address problems or opportunities or manage the situation at hand by drawing on one's knowledge and experience base and calling on other references and resources as necessary.Quality: Prioritizes and delivers highest levels of quality in work and interactions with customers and team members.Self-Awareness: Self-Aware, open to coaching and self-improvement, agile and decisive in decisions. Is highly effective socially and interpersonally- adept at interpreting social and emotional cures and adapting approach and messaging accordingly.Training Others: Carefully and fully articulates methods and approaches in a way that is understood by using delivery mechanisms that meet the needs of the learner.Written Communication: Conveys ideas and facts in writing in a way that will be understood by composing in a clear, direct, concise and complete manner.  skills: Analytical 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.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: This position performs routine and non-routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements. This role provides laboratory troubleshooting for a team to assist in the successful and timely execution of laboratory analyses.   location: Greenville, North Carolina job type: Permanent salary: $70,000 - 80,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Analytical Testing: With limited supervision, perform a broad array of primary and advanced analytical testing methods (wet and dry chemistry) in compliance with all cGMP and regulatory guidelines and ensure the highest standards for efficiency, right first-time measures, and quality standardsClient Service: Support and sometimes participate in the direct interaction with client organizations to assure timely and complete reporting, problem-solving and the highest level of service and responsivenessData Integrity: Ensure integrity of data through accurate transactions, documentation, and tracking of all cGMP activitiesData Interpretation and Problem-Solving: Use appropriate resources (e.g. software) toinvestigate and interpret data in support of recommendations for problem-solving related to methods, instruments and analytical techniques.Process Improvement: Identify and recommend opportunities for improved efficiencies, client service and teamwork within the analytical groupQuality: Ensure the quality of work, products and services as a first priority; comply with or exceed all regulatory and cGMP compliance standards as well as ensure accuracy of analyses as it relates to right first time measuresSafety: Adhere to all workplace safety laws, regulations, standards, and practices and actively advance a culture of safety within his or her team and organization.Independently perform routine and complex testing for chromatographic and spectrophotometric methods (HPLC, GC, UV) of analysis for excipients, new chemical entities and/or drug productsInterpret data and make recommendations to management for improvement or potential concernsCompare laboratory data against specifications, prepare reports, and trend data where applicable to determine if results meet requirementsEnsure proper usage, care, and return of calibration standards including, but not limited to, reference standards, timers, thermometers, and instrumentationEnsure accuracy of testing by following method/standard instructions and adhering to internal SOPs to eliminate the potential for repeat testing, deviations, and investigationsIndependently author standard operating procedures, analytical testing procedures, final submission ready documents, and create document templates for use by junior team membersCreate report templates and/or enter data into established reports/templates or software-based systemsReview routine laboratory experiments for accuracy and provide guidance to junior team members to ensure future complianceIdentify and recommend opportunities for improved efficiencies, internal/external client service and teamwork within the analytical groupServe as a point of contact for laboratory testing support and provide updates to laboratory supervision and/or clientWith supervision, support the scheduling and planning of internal/external client project work to ensure the highest levels of efficiency and quality standards are metSupport the development of a climate of quality within the teams by driving and monitoring quality standards within the teamBecome resident expert in the use of Empower (perform supervisory sign-off for electronic reports) and other software-based systemsServe as a method troubleshooting resource to identify and document critical factors that affect method performance and assist peers in resolving method issues in a timely, cost-effective mannerIndependently perform method evaluation/development/validation and troubleshooting instruments and improvement of processesAssist laboratory management with the preparation and execution of laboratory investigations/deviations and CAPA within the electronic quality system (eQMS)Mentor and train new laboratory team members  qualifications: Analytical Acumen: Skilled in the interpretation and application of data in problem-solving, decision-making, account planning, and activity prioritization.Decision Quality: Considers all relevant factors (analysis, wisdom, experience and judgment) and uses appropriate decision-making criteria and principles.Equipment Operation: Is skilled in the use and trouble-shooting of key equipment important in the delivery of the job.Problem Solving: Build a logical approach to address problems or opportunities or manage the situation at hand by drawing on one's knowledge and experience base and calling on other references and resources as necessary.Quality: Prioritizes and delivers highest levels of quality in work and interactions with customers and team members.Self-Awareness: Self-Aware, open to coaching and self-improvement, agile and decisive in decisions. Is highly effective socially and interpersonally- adept at interpreting social and emotional cures and adapting approach and messaging accordingly.Training Others: Carefully and fully articulates methods and approaches in a way that is understood by using delivery mechanisms that meet the needs of the learner.Written Communication: Conveys ideas and facts in writing in a way that will be understood by composing in a clear, direct, concise and complete manner.  skills: Analytical 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.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.
    • greenville, north carolina
    • permanent
    • $55,000 - $60,000 per year
    job summary: This position is responsible for independently performing routine and non-routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements.   location: Greenville, North Carolina job type: Permanent salary: $55,000 - 60,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Key Responsibility Areas Analytical Testing: With limited supervision, perform a broad array of primary and advanced analytical testing methods (wet and dry chemistry) in compliance with all cGMP and regulatory guidelines and ensure the highest standards for efficiency, right first-time measures, and quality standardsData Interpretation and Problem-Solving: Use appropriate resources (e.g. software) to investigate and interpret data in support of recommendations for problem-solving related to methods, instruments and analytical techniquesProcess Improvement: Identify and recommend opportunities for improved efficiencies, client service and teamwork within the analytical groupQuality: Ensure the integrity of data, quality of work, products and services as a first priority; complies or exceeds all regulatory and cGMP compliance standards as well as ensure accuracy of analyses as it relates to right first-time measuresSafety: Adhere to all workplace safety laws, regulations, standards, and practices and actively advance a culture of safety within his or her team and organizationIndependently perform routine and complex testing for chromatographic and spectrophotometric methods (HPLC, GC, UV) of analysis for excipients, new chemical entities and/or drug productsCompare laboratory data against specifications and trend data where applicable to determine if results meet requirementsInterpret data and make recommendations to management for improvement or potential concernsCreate report templates and/or enter data into established reports/templates or software-based systemsUnder general supervision, author standard operating procedures, analytical testing procedures, final submission ready documents, and create document templates for use by junior team membersWith guidance, propose applicable specifications based on data obtained in support of certain programsEnsure proper usage, care, and return of calibration standards including, but not limited to, reference standards, timers, thermometers, and instrumentationEnsure accuracy of testing by following method/standard instructions and adhering to internal SOPs to eliminate the potential for repeat testing, deviations, and investigationsDirect and assist in laboratory personnel training when requiredUnder general supervision, evaluate and validate methods of analysis for chemical entities and drug product formulationsProvide assistance with method development to ensure methods are robust and able to be validatedMay serve as a technical liaison between functional groups such as Quality Assurance and metrologyConduct peer review of routine and complex laboratory experiments for accuracy and provide guidance to junior team members to ensure future complianceMaintain proficient knowledge in the use of Empower and other software-based systems; perform supervisory sign-off for electronic reports  qualifications: Attention to Detail: Thoroughness in accomplishing a task through concern for all the areas involved, no matter how small. Monitors and checks work or information and plans and organizes time and resources efficiently.Equipment Operation: Is skilled in the use and trouble-shooting of key equipment important in the delivery of the job. Listening: Active listening, hearing and learning from what others say.Operating Equipment: Understands and promotes the effective and full utilization of tools, machines, and equipment in the performance of their roles.Organization: Establish a systematic course of action for self or others to ensure accomplishment of a specific objective; set priorities, goals, and timetables to achieve maximum productivity.Quality: Prioritizes and delivers highest levels of quality in work and interactions with customers and team members.Technical Learning: Picks up on technical things quickly; can learn new skills and knowledge; is good at learning new industry, company, product, or technical knowledge; does well in technical courses and seminars.Training  skills: Analytical 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.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: This position is responsible for independently performing routine and non-routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements.   location: Greenville, North Carolina job type: Permanent salary: $55,000 - 60,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Key Responsibility Areas Analytical Testing: With limited supervision, perform a broad array of primary and advanced analytical testing methods (wet and dry chemistry) in compliance with all cGMP and regulatory guidelines and ensure the highest standards for efficiency, right first-time measures, and quality standardsData Interpretation and Problem-Solving: Use appropriate resources (e.g. software) to investigate and interpret data in support of recommendations for problem-solving related to methods, instruments and analytical techniquesProcess Improvement: Identify and recommend opportunities for improved efficiencies, client service and teamwork within the analytical groupQuality: Ensure the integrity of data, quality of work, products and services as a first priority; complies or exceeds all regulatory and cGMP compliance standards as well as ensure accuracy of analyses as it relates to right first-time measuresSafety: Adhere to all workplace safety laws, regulations, standards, and practices and actively advance a culture of safety within his or her team and organizationIndependently perform routine and complex testing for chromatographic and spectrophotometric methods (HPLC, GC, UV) of analysis for excipients, new chemical entities and/or drug productsCompare laboratory data against specifications and trend data where applicable to determine if results meet requirementsInterpret data and make recommendations to management for improvement or potential concernsCreate report templates and/or enter data into established reports/templates or software-based systemsUnder general supervision, author standard operating procedures, analytical testing procedures, final submission ready documents, and create document templates for use by junior team membersWith guidance, propose applicable specifications based on data obtained in support of certain programsEnsure proper usage, care, and return of calibration standards including, but not limited to, reference standards, timers, thermometers, and instrumentationEnsure accuracy of testing by following method/standard instructions and adhering to internal SOPs to eliminate the potential for repeat testing, deviations, and investigationsDirect and assist in laboratory personnel training when requiredUnder general supervision, evaluate and validate methods of analysis for chemical entities and drug product formulationsProvide assistance with method development to ensure methods are robust and able to be validatedMay serve as a technical liaison between functional groups such as Quality Assurance and metrologyConduct peer review of routine and complex laboratory experiments for accuracy and provide guidance to junior team members to ensure future complianceMaintain proficient knowledge in the use of Empower and other software-based systems; perform supervisory sign-off for electronic reports  qualifications: Attention to Detail: Thoroughness in accomplishing a task through concern for all the areas involved, no matter how small. Monitors and checks work or information and plans and organizes time and resources efficiently.Equipment Operation: Is skilled in the use and trouble-shooting of key equipment important in the delivery of the job. Listening: Active listening, hearing and learning from what others say.Operating Equipment: Understands and promotes the effective and full utilization of tools, machines, and equipment in the performance of their roles.Organization: Establish a systematic course of action for self or others to ensure accomplishment of a specific objective; set priorities, goals, and timetables to achieve maximum productivity.Quality: Prioritizes and delivers highest levels of quality in work and interactions with customers and team members.Technical Learning: Picks up on technical things quickly; can learn new skills and knowledge; is good at learning new industry, company, product, or technical knowledge; does well in technical courses and seminars.Training  skills: Analytical 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.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.
    • greenville, north carolina
    • permanent
    • $90,000 - $100,000 per year
    job summary: This position leads and supports formulation and process development activities while serving as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. This role is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation.   location: Greenville, North Carolina job type: Permanent salary: $90,000 - 100,000 per year work hours: 8 to 4 education: Masters   responsibilities: People Development: Lead in the development of a culture, and supporting systems, to drive open communication, participation, and idea-sharing in order to build an engaged team, advances and models Mayne Pharma values and leadership commitmentsPharmaceutical Development: Manage formulation development activities to develop stable and robust formulations, using Quality by Design PrinciplesProcess Optimization: Identify and recommend opportunities for improved efficiencies and teamwork across the Pharmaceutical Development groupScientific Excellence: Design and execute experiments in support of potential new technological offerings as well as participate or support research articles and publications Specific Responsibilities Responsibilities include, but are not limited to: Independently design, coordinate, and execute all product development activities including material characterization, excipient selection, prototype manufacture, equipment selection, generation of batch records, scale-up, QbD, and registration batch activitiesWork closely with analytical scientists, project management, quality and commercial operations to ensure that formulation and process development are appropriate and timelyWrite all the required documentations such as batch records, product development reports, risk assessments, and campaign summariesCommunicate effectively with internal staff, clients, and external vendorsResponsible for GMP compliance in formulation and process developmentSupport and contribute to qualification of facility and equipmentCoordinate with logistics and scheduling groups to help ensure that an adequate inventory of raw materials is maintained at all timesMaintain competence and training documentation for relevant equipment and processes  qualifications: Agile & Flexible: Leads and embraces change. Fosters innovation by challenging the status quo and initiating new ways of working.Celebrator: Embraces a culture of action. Sets challenges and achieves results. Celebrates and rewards achievements of team members.Communicator/Collaborator: Builds shared meaning through open and respectful communication. Engages stakeholders in pertinent conversations, and creates an atmosphere that is inclusive and consultative.Leads Self: Maximizes personal potential by focusing on ongoing professional growth. Takes initiative, honors promises, and acts with courage.People Developer: Empowers, inspires, and challenges team members. Fosters high performance and development.Purpose Driven: Drives vision and purpose by creating and contributing to strategic direction. Aligns priorities to organizational goals.Solutions Focused: Solves problems once and simplifies issues. Makes problems visible and acts decisively.Team Builder: Builds and optimizes a high performing team. Creates a sense of belonging and connectivity among team members.Conflict Resolution: Bring substantial conflicts and disagreements into the open and attempt to manage them collaboratively, building consensus, keeping the best interests of the organization in mind, not only one's own interestLeadership: Motivate others, share knowledge, drive high performing teams, show respect towards others and provide constructive feedbackPh.D. in Pharmaceutical Science or related field or Pharm.D. with at least 4 years of industrial product development experienceMaster's degree in pharmaceutical science, chemistry, or related science with at least 5 years of industrial pharmaceutical experienceBachelor's degree in pharmaceutical science, chemistry, engineering or related science with at least 6 years of industrial pharmaceutical experience  skills: 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.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: This position leads and supports formulation and process development activities while serving as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. This role is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation.   location: Greenville, North Carolina job type: Permanent salary: $90,000 - 100,000 per year work hours: 8 to 4 education: Masters   responsibilities: People Development: Lead in the development of a culture, and supporting systems, to drive open communication, participation, and idea-sharing in order to build an engaged team, advances and models Mayne Pharma values and leadership commitmentsPharmaceutical Development: Manage formulation development activities to develop stable and robust formulations, using Quality by Design PrinciplesProcess Optimization: Identify and recommend opportunities for improved efficiencies and teamwork across the Pharmaceutical Development groupScientific Excellence: Design and execute experiments in support of potential new technological offerings as well as participate or support research articles and publications Specific Responsibilities Responsibilities include, but are not limited to: Independently design, coordinate, and execute all product development activities including material characterization, excipient selection, prototype manufacture, equipment selection, generation of batch records, scale-up, QbD, and registration batch activitiesWork closely with analytical scientists, project management, quality and commercial operations to ensure that formulation and process development are appropriate and timelyWrite all the required documentations such as batch records, product development reports, risk assessments, and campaign summariesCommunicate effectively with internal staff, clients, and external vendorsResponsible for GMP compliance in formulation and process developmentSupport and contribute to qualification of facility and equipmentCoordinate with logistics and scheduling groups to help ensure that an adequate inventory of raw materials is maintained at all timesMaintain competence and training documentation for relevant equipment and processes  qualifications: Agile & Flexible: Leads and embraces change. Fosters innovation by challenging the status quo and initiating new ways of working.Celebrator: Embraces a culture of action. Sets challenges and achieves results. Celebrates and rewards achievements of team members.Communicator/Collaborator: Builds shared meaning through open and respectful communication. Engages stakeholders in pertinent conversations, and creates an atmosphere that is inclusive and consultative.Leads Self: Maximizes personal potential by focusing on ongoing professional growth. Takes initiative, honors promises, and acts with courage.People Developer: Empowers, inspires, and challenges team members. Fosters high performance and development.Purpose Driven: Drives vision and purpose by creating and contributing to strategic direction. Aligns priorities to organizational goals.Solutions Focused: Solves problems once and simplifies issues. Makes problems visible and acts decisively.Team Builder: Builds and optimizes a high performing team. Creates a sense of belonging and connectivity among team members.Conflict Resolution: Bring substantial conflicts and disagreements into the open and attempt to manage them collaboratively, building consensus, keeping the best interests of the organization in mind, not only one's own interestLeadership: Motivate others, share knowledge, drive high performing teams, show respect towards others and provide constructive feedbackPh.D. in Pharmaceutical Science or related field or Pharm.D. with at least 4 years of industrial product development experienceMaster's degree in pharmaceutical science, chemistry, or related science with at least 5 years of industrial pharmaceutical experienceBachelor's degree in pharmaceutical science, chemistry, engineering or related science with at least 6 years of industrial pharmaceutical experience  skills: 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.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.

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