Pharmaceutical Quality Assurance Manager Jobs in San Francisco, California

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110 San Francisco, CA Pharmaceutical Quality Assurance Manager jobs found on Monster.

Jobs 1 to 20 of 110
QA Product Technical Manager/Sr. QA Product Technical Manager Requisition ID -00431765 The Position Perform final review, cumulative review and disposition of Genentech manufactured cell banks and clinical drug substance, drug product and final drug product. Review and approve procedures, tickets and other clinical QA controlled documentation. Provide clinical trial support such as COA/COC/C...
Our client in South San Francisco is looking for a Senior QA Associate to join their team! Senior Quality Assurance Associate Duties: Responsible in supporting all functional Quality Assurance activities related to the disposition of all company's products for clinical and commercial use under the direction of the Senior Manager, QA Product Disposition Review and compile executed batch documen...
Streffco Consultants, Inc. San Francisco, CA
Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Quality Assurance Associate III (Quality Engineering On the Floor) Job ID: 6322 Industry: Biotech/Pharmaceutical Location: Research Triangle Park, NC Duration: 9 Month Contra...
Description Senior Manager/Associate Director, Clinical Quality Assurance Compliance 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 Senior Manager/Associate Director, Clinical Quality Assurance Compliance. The Senior Ma...
Responsible for performing a wide variety of activities pertaining to assuring product quality and compliance to regulatory requirements in the manufacture, testing and control, and release of pharmaceutical drug substance and drug product used for commercial products and clinical distribution. This work includes but limited to: Perform review of batch record and test records in a timely fashion ...
Searchamericanjobs San Francisco, CA
Line of Service:Advisory Industry:Healthcare Services State & City:VA-McLean TX-Dallas PA-Philadelphia NY-New York NY-Albany MA-Boston IL-Chicago GA-Atlanta FL-Tampa DC-Washington CA-San Francisco CA-Los Angeles Travel Requirements:21-40% Position Type:Full Time Auto req ID:64928BR-1 PwC/LoS Overview: Are you interested in the opportunity to work for an industry-leading firm that...
Manager, Regulatory Compliance (Clinical Trials/Quality Assurance) Requisition ID -2523713828 The Position This position is responsible for assuring overall regulatory compliance with FDA Quality System Regulations, Medical Device Directives, and ISO standards. This includes oversight of Global Regulatory Compliance programs and processes, including Medical Device Reporting (MDR), Medical Devi...
Description Senior Specialist/Manager, Clinical Quality Assurance Operations 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 Senior Specialist/Manager, Clinical Quality Assurance Operations. The position’s main responsibi...
Description Senior Manager, Clinical Quality Assurance Operations 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 Senior Manager, Clinical Quality Assurance Operations. This position will play an essential role in the co...
Grifols, Inc. Emeryville, CA
Overview: The incumbent will be responsible for activities associated with managing the deviation / CAPA department within Quality Assurance. Review deviation reports for technical and factual accuracy, compliance to local procedures and regulatory requirements; track status of outstanding deviations; distribute routine status reports to management; organize cross-functional meetings to facilitat...
Grifols, Inc. Emeryville, CA
Overview: An individual contributor role supporting deviation and CAPA resolution within Quality Assurance. The incumbent will be responsible for activities associated with deviation resolution. Review deviation reports for technical and factual accuracy, compliance to local procedures and regulatory requirements; track status of outstanding deviations, provide support to the investigation proces...
Associate Director, IMP QA Operations Requisition ID -2513737539 The Position The IMP Quality Operations – US and Asia Pacific department is a part of the larger PTD Global Quality Organization. The group is responsible for the quality oversight of GMP activities within the US and Asia Pacific regions. The Associate Director of IMP QA Operations- US and Asia Pacific will be providing leadersh...
Qa Specialist Requisition ID -2964169958 The Position Main Purpose of the Position: ·Independently lead/participate on GMP compliance audits and identify GMP compliance gaps or risks. ·Provide GMP Compliance expertise to customers. ·Develop solutions to complex issues and Quality initiatives with inter-organizational impact, following cGMP regulations and Genentech standards ·Perform tasks...
Duration: 3 months Job Description: Client Specialty Health is seeking a mid-level QA Engineer who will work with a team of developers and business users to test software releases and support customer-facing applications under the supervision of the QA Manager. This resource will need to interact with developers, business and management to ensure requirements are fully understood and tested. - ...
Duration: 3-4 months Description: Client is seeking a mid-level QA Engineer who will work with a team of developers and business users to test software releases and support customer-facing applications under the supervision of the QA Manager. This resource will need to interact with developers, business and management to ensure requirements are fully understood and tested. - Responsible for fu...
QA Sr. Specialist-Investigator Requisition ID -2956323113 The Position Manage and lead complex discrepancies and investigations to ensure timely completion and supported conclusions Apply extensive theoretical and cross-functional expertise in the context of company objectives to independently address complex problems Work on complex issues where analysis of situations or data requires an in...
Senior QA Specialist Requisition ID -00432403 The Position Position Summary The primary responsibility of this position will be to ensure compliance to the Roche Pharmaceutical Quality System (PQS) quality assurance directives, global policies and standards. This role will be responsible for the development and implementation of QA review and monitoring processes to document on-going GBQC PQ...
ProPharma Group San Francisco, CA
At ProPharma Group, we work with clients in the pharmaceutical, biotechnology and medical device industries to provide the best solutions for their unique challenges and concerns. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes. Our goal is to provide the information our clients need to deliver safe, effective and q...
Director Design Quality Assurance Requisition ID -2509492100 The Position Strong interface with Quality Management, Regulatory, Research, Development, and Clinical Operations to assure all products and processes are in accordance with company standards and quality systems. This is accomplished through Strategic Quality Planning, Quality System execution and maintenance, non-conformance, correc...
BioScreen Testing Services, Inc. San Francisco, CA
Quality Assurance Specialist Schedule: 40 hours per week with a minimum of 4 hours on Saturdays. BioScreen Testing Services, Inc. a well-established consumer product-testing laboratory, providing services to the Pharmaceutical/ Biotech, Medical Device and OTC/Personal Care industry is currently seeking a Quality Assurance Specialist. Growing GMP laboratory has immediate opening for a QA Special...

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