Pharmaceutical Quality Assurance Manager Jobs in San Francisco, California
74 San Francisco, CA Pharmaceutical Quality Assurance Manager jobs found on Monster.Jobs 1 to 20 of 74
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...
Provide support for Company regulatory inspections, client qualification audits and routine/ad hoc audits; conduct external qualification and ongoing audits of vendors and client partners as needed Recommend changes in standard procedures to reflect technological changes, regulatory trends and best practices Provide support and assist in the development and management of quality systems at DLSS ...
Theravance Inc. South San Francisco, CA, 94080
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 ...
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...
Medivation San Francisco, CA, 94118
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...
Manage and administer all aspects of people processes related to the employee life cycle. This includes the selection, hiring and training of personnel on company and department policies, systems and processes. Manage and communicate compensation related information per company guidelines. · Coach and develop staff by providing an environment that encourages ongoing personal and professional deve...
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...
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...
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...
The Sr. Manager, Product Quality Management (PQM) is primarily responsible for coordination, implementation, and execution of Product Complaints, Recalls, and Inspection Readiness. The Sr. Manager will also provide guidance on Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) for Onyx departments, groups, partners and alliance partners to help identify and proactively manage...
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...
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...
Based in South San Francisco, California, Onyx Pharmaceuticals is an Amgen subsidiary, engaged in the development and commercialization of innovative therapies for improving the lives of people with cancer. At Onyx, our success begins with our employees. The progress we have made as a company reflects the talents of the individuals who have come together to develop possible new therapeutics for tr...
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...
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 leadership, vision, and direction to the group. The position is responsible for allocating...
Utter Health Sacramento San Francisco, CA
SHSSR-1440042Coordinator, Research Billing amp; Quality Assurance Description The Research Billing and Quality Assurance Coordinator (RBQAC) implements, manages and oversees development, review and training of policies and procedures to ensure departmental compliance with FDA guidelines and International standards for Good Clinical Practice as they apply to all aspects of the billing practice an...
Principal Technical Manager, External Quality - Development Small Molecules Requisition ID -00420654 The Position The purpose of this position is to provide technical quality support to the External Quality Clinical (IMPs) Small Molecules and to the appropriate stakeholders. This position leads quality system development and implementation as well as business process improvements. The incumben...
Manager, Quality Requisition ID -00432535 The Position Main Purpose of the Position: ·Manage the planning, preparation, and conduct of Quality Assurance staff performing a variety of routine and complex oversight activities that meet cGMP regulations and Genentech standards. ·Manage performance and development of direct reports to ensure achievement of organizational and department goals and...
Interactive Marketing Portfolio Quality Manager/Sr. Manager Requisition ID -00433159 The Position TheQuality Managerserves as a subject matter expert on multichannel marketing campaign quality assurance/control activities as well as to act as a strategic advisor on portfolio level initiatives that enable improved delivery efficiency and cross-team collaboration. Interactive Marketing (IM) Por...
Principal Site Mgr Combination Product Device, External Quality, North America Requisition ID -2962876129 The Position Location: San Francisco REPORTS TO: Head of Devices and Combination Products, North America Position Purpose; The Principal Technical Manager position will provide Quality oversight for Roche/Genentech products and drug delivery systems manufactured at Contract Manufacturin...
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Quality Assurance Manager - Pharmaceuticals
$48,000.00 - $127,680.00
Typical Salary for Quality Assurance Manager - Pharmaceuticals in San Francisco
Source: Monster.com Careerbenchmarking Tool
Education / Training
Some College Coursework Completed
Source: Monster.com Careerbenchmarking Tool
Quality Assurance Manager - Pharmaceuticals
Assures consistent quality of pharmaceuticals production by developing and enforcing good automated manufacturing practice (GAMP) systems; managing staff.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Attention to Detail
Validates quality processes by establishing product specifications and quality attributes; measuring production; documenting evidence; determining operational and performance qualification; writing and updating quality assurance procedures.
Achieves quality assurance operational objectives by identifying and resolving problems; completing audits; determining system improvements; implementing change.
Popular Pharmaceutical Quality Assurance Manager Articles
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