Full-Time Manager jobs in the Quality Assurance & Safety category and Biotechnology & Pharmaceuticals industry

With over $1 billion in annual revenues and 13,000 employees across 170 sites in 35 countries, Eurofins is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, food, environmental and consumer products industries and to governments. Eurofins is searching for an Operational Excellence LEAN Project Manager to lead global...
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Position Description: There is no greater calling or opportunity for a fluid management company than today’s challenge – helping customers protect people, the environment and our natural resources. Together we are implementing technologies that purify and conserve water, consume less energy, make alternative energy sources possible and practical, advance medicine and minimize emissions and waste. ...
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JOB SUMMARY: The Sr. Principal Specialist, in interaction with Management, is responsible for the development, implementation and management of specific audit activities and programs. These programs are designed to support stated goals for identified development activities both within the CSO Platform and to outside providers including investigators and CROs. The Sr. Principal Specialist is also r...
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Catalent Pharma Solutions (a Blackstone Group company) is a leading Drug Development, Advanced Delivery Technology and Supply partner to the global pharmaceutical industry. A Fortune 1000 company, with over 20 locations on 5 continents, we partner with 90 out of the top 100 pharmaceutical companies and 44 of the top 50 biotech firms, as well as thousands of small innovator companies. I. Essential ...
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Requisition ID 14538BR Title Senior Quality Associate, Quality Management- Dallas, TX Job Category Clinical Job Description PURPOSE: Provide feedback to CRAs and their managers based on findings during on-site visits. Discuss trends and findings with CRA Manager/Director of Field Management and/or Associate Director for CTM Quality to identify individual and department training needs, and assure a...
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Sr. Quality Engineer Medical Devices A Quality Assurance Manager with medical device manufacturing experience is needed in western Massachusetts with a strong and growing medical products (devices, pharma, and combination products) company. This position carries responsibility for manufacturing quality, quality systems, and compliance within the manufacturing facility. This is a position for a lea...
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Job Summary: The Principal Specialist is responsible for the initiation, conduct, and follow-up of audits as assigned by CQA Management. Within the frame of the Principal Specialist's mission and responsibilities, the audits and activities require proven ability to independantly interact with all internal and external (e.g. Vendors / CRO) operational staff (e.g. Project Teams, Clinical Operations,...
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Company Overview: Lilly is the 10th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 135 years. Across the globe, we are a leader in investing in research and development and we also invest in our employees – in competitive salaries, training and development, and health. The pharmaceutical industry is a complex, r...
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The Wright Group, a leading global vitamin and mineral blending company, is currently accepting resumes for a fulltime Quality ControlLaboratory Analyst. This position is responsible for the handling and analysis of samples received into the laboratory. The Lab Analyst completes reliable analyses by adhering to standard operating procedures (SOPs), good laboratory practices (GLP), and current good...
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Description Advanced Sterilization Products (ASP), a Division of Johnson & Johnson's Global Medical Solutions Group is recruiting for two Quality Technician Lead, located in Mira Loma, CA. ASP (Advanced Sterilization Products), a member of the Johnson & Johnson Family of Companies, is a leading designer and developer of innovative instrument sterilization, high-level disinfection and cleaning tech...
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Catalent Pharma Solutions (a Blackstone Group company) is a leading Drug Development, Advanced Delivery Technology and Supply partner to the global pharmaceutical industry. A Fortune 1000 company, with over 20 locations on 5 continents, we partner with 90 out of the top 100 pharmaceutical companies and 44 of the top 50 biotech firms, as well as thousands of small innovator companies. SUMMARY OF ES...
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. The Principal Quality Engineer works independently with little to no supervision and exercises considerable discretion in determining objectives of and approaches to significant organizational projects or assignments. The Principal Quality Engineer works closely with other cross-functional teams including QA, QC, Manufacturing, Facilities/Engineering, MTS, Planning/Logistics to provide guidance ...
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Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas o...
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Quality Auditor Principal Schedule and conduct internal audits,support external agency inspections (e.g. FDA, EMA, TGA and others), and external vendor/supplier audits and inspections. Prepare audit reports and initiate the subsequent corrective action requests. Assist in the management of external audits. Responsible to track and trend key audit program metrics, and to report at management review...
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Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas o...
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Description Position Summary: Plan and direct activities concerned with the design, development, application, implementation and maintenance of quality standards to ensure that all new and existing products meet their requirements for safety and effectiveness. Position Responsibilities: Ensure that all new products and changes to existing products and processes are formally validated, documents an...
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Johnson & Johnson companies are equal opportunity employers. SENIOR DIRECTOR, QUALITY OPERATIONS-00000CVS Description Vision Care, a member of Johnson & Johnson&'s Global Medical Solutions Organization, is recruiting for a Senior Director, Quality Operations. The preferred location for this position is Jacksonville, Florida, however this position can also be located in Limerick, Ireland. The Senio...
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Johnson & Johnson companies are equal opportunity employers. SR. EHS SPECIALIST-8234130226 Description For more than 30 years, Janssen Biotech, Inc. has delivered on the promise of new treatments and ways to improve the health of individuals with serious disease. Built upon a rich legacy of innovative firsts, Janssen Biotech, Inc. pursues innovative solutions in the therapeutic areas of immunology...
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Johnson & Johnson companies are equal opportunity employers. GROUP LEADER EH&S-5957130415 Description Advanced Sterilization Products Division of Ethicon, Inc., a member of Johnson & Johnson&'s Family of Companies, is currently recruiting for a Group Leader EH&S, located in Irvine, CA. ASP (Advanced Sterilization Products), a member of the Johnson & Johnson Family of Companies, is a leading design...
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. QC Investigator, Principal Department Description: Quality Control Microbiology Department supports manufacturing activities at Genzyme Allston Landing by detecting, quantifying and identifying possible contaminants that may interfere with the quality of the product during the different stages of the manufacturing process. It aims to maintain a state of microbiological control in the Utility Sys...
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Job ID: 211 Position Description: Our Jersey City, NJ office has an exciting opportunity available in our Quality Assurance Department as a GCP Auditor. The main responsibility of this position is conducting internal and external GCP/GLP Compliance auditing activities. The role is approximately 95% GCP and 5% GLP. This position reports into the Sr. Manager, GCP/GLP Compliance and does not have any...
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Job ID: 400 Position Description: The GMP Compliance Specialist is responsible for routine GMP Audits which entails performing specialty and technical audits and review in relation to current products and prospective in-license agreements, providing compliance support to sites and the QA organization, training delivery, and leading multi-departmental teams and initiatives. This position reports to...
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A leading global Biotech organization is currently recruiting for a Product Complaints Quality Control Associate I position based in Cambridge, MA. This is a 6 month contract paying a generous hourly rate plus overtime. This position is interviewing immediately and can start as soon as possible. The primary responsibility for this position is to provide technical and administrative support within ...
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. Quality Control Chemistry is responsible for testing intermediate and final product samples to demonstrate that all products meet all standards required for cGMP operations. Various techniques are utilized in Quality Control including HPLC, GC, Gel Electrophoresis and multiple types of spectrophotometry. Additional functions include raw material testing, stability testing, assay transfers and th...
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Johnson & Johnson companies are equal opportunity employers. PROCESS EXCELLENCE SPECIALIST-0149130125 Description McNeil Consumer Healthcare, a member of Johnson & Johnson&'s Family of Companies, is recruiting for a Process Excellence Specialist located in Lancaster, PA. McNeil Consumer Healthcare Division of McNEIL-PPC, Inc markets a broad range of over-the-counter products, including TYLENOL® ac...
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