Biotech Quality Assurance Specialist Jobs

110 jobs

Senior Manager, Quality Systems: Attractive and Growing Biotech., NJ/NYC area Summary: We are working with a very attractive Biotech that is rapidly growing and stable. They have a newly created opening for a Senior Manager, Quality Systems. Given that this is a smaller organization, you will not be pigeon-holed and will have the opportunity to handle a diverse amount of Quality Systems responsib...

Quality Assurance Specialist II/III (Needham, MA) Overview: The QA Specialist II/III supports Quality Assurance functions focused on GMP manufacturing operations. The position will review/audit complex documents including batch records and QC data; ensure compliance to defined Quality System procedures; conduct moderate level information analysis; assure compliance to specifications and standard...

CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply QA Validation Specialist - Pharma, SQL West Caldwell, NJ Contract Unspecified Apply Apply QA Validation Specialist - Pharma, SQL West Caldwell, NJ Contract Unspecified Apply Job Details If you are a QA Validation Specialist with Pharma and SQL experience, please read on! What You Will Be Doing ...

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. The position...

Must have: - Bachelor’s degree in science or engineering or equivalent - A minimum of 6-8 years experience in a biotech or pharmaceutical Quality Assurance environment - Ability to coordinate and lead diverse audit teams in evaluation of GMP facilities and quality systems - Audit experience of drug product and drug substance manufacturers, raw material suppliers, testing laboratories, cell ban...

The successful candidate will be: An experienced Quality Auditor with experience in managing and executing internal, external and vendor audits in the pharmaceutical, biotech, or medical device industry. Have a strong working knowledge of GMP regulations and quality regulatory requirements in a cGMP manufacturing environment (FDA, EMA and other cGMP regulations and guidelines). Must be able to ...

Company Description Radiometer - Make an impact on life. The difference between life and death can be just a few minutes. Radiometer’s diagnostic equipment is of crucial importance to doctors all over the world in their effort to diagnose critically ill patients quickly and accurately. From biotech and software specialists to financial controllers and engineers, all 2500 colleagues are committed a...

Summary: Expedite contract negotiation and execution by acting as a resource and liaison for the Contracts and Grants group to streamline requests to law department and avoid duplication of efforts among Contract & Grants Analysts (CGAs) and CGA management. Act as main point of contact with legal department to resolve complex legal issues while ensuring compliance with company process and strateg...

Summary: Expedite contract negotiation and execution by acting as a resource and liaison for the Contracts and Grants group to streamline requests to law department and avoid duplication of efforts among Contract & Grants Analysts (CGAs) and CGA management. Act as main point of contact with legal department to resolve complex legal issues while ensuring compliance with company process and strateg...

Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of cancer. Merrimack seeks to gain a deeper understanding of underlying cancer biology through its systems biology-based approach and develop new insights, therapeutics and diagnostics to improve outcomes for cancer patients. Merri...

Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of cancer. Merrimack seeks to gain a deeper understanding of underlying cancer biology through its systems biology-based approach and develop new insights, therapeutics and diagnostics to improve outcomes for cancer patients. Merri...

This is a senior-level individual contributor role, responsible for providing direct Quality Assurance (QA) oversight of BI’s drug product CMO/s and in-house drug manufacturing at Boehringer Ingelheim Fremont. Incumbent makes complex decisions independently with little time for deliberation, which may have a direct impact on active manufacturing operations, equipment, facility, systems, or areas. ...

Job Description This is a senior-level individual contributor role, responsible for providing direct Quality Assurance (QA) oversight of BI’s drug product CMO/s and in-house drug manufacturing at Boehringer Ingelheim Fremont. Incumbent makes complex decisions independently with little time for deliberation, which may have a direct impact on active manufacturing operations, equipment, facility, sy...

Description Specialist / Senior Specialist, Clinical Quality Assurance Compliance (Contract) Medivation, Inc. (NASDAQ: MDVN – www.medivation.com) is a publicly traded biopharmaceutical company located in San Francisco. We are currently seeking a qualified, highly motivated, experienced individual for the position of Specialist / Senior Specialist, Clinical Quality Assurance Compliance (Contract)...

PLEASE NOTE: * This is a night shift position. * This position works on a 12 hour shift schedule that includes working every other weekend. Responsible for assuring the quality of commercial and clinical products manufactured at the facility. Supports functional areas including manufacturing, facilities and other Quality departments. Implements quality policies for process improvements. Utilize...

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...

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...

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...

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...

Sr. Specialist- QA Engineering 10051BR Technical Operations Quality (10000938) Regular SRPR I United States - MA - Lexington Quality Assurance Primary Role This individual will be responsible for providing senior level quality assurance for the Facilities, Engineering and Validation functions for Shire internal (US) drug substance manufacturing sites. This is a senior individual contribut...