Pharmaceutical Quality Assurance Manager Jobs in California

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344 California Pharmaceutical Quality Assurance Manager jobs found on Monster.

Jobs 1 to 20 of 344
Johnson & Johnson companies are equal opportunity employers. MANAGER QUALITY ASSURANCE - QUALITY EXCELLENCE-3156140824 Description Johnson & Johnson Los Angeles Plant is seeking a Manager of Quality Assurance (Quality Excellence), to be located in Los Angeles, CA. Johnson & Johnson Los Angeles Plant develops and markets consumer healthcare, baby care, and beauty/skin care products that address...
Quality Assurance Manager: Precision Measurements, Inc. is an ISO 9001:2008 Quality certified and ISO 17025 Accredited Metrology Laboratory located in San Jose, California – the heart of Silicon Valley. PMI has been providing quality metrology services for over 30 years for a wide range of Electronic, Analytical, Mechanical / Dimensional Measuring and Test Equipment. We specialize in the fields o...
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...
POSITION SUMMARY Responsible for managing various facets of quality projects related to submissions to the FDA, review and approval of Validation documents and the management of Methods Validation. ESSENTIAL DUTIES and RESPONSIBILITIES include the following. Other duties may be assigned. Develop quality objectives, manage, and maintain project plans. Interface with various groups to ensure tha...
PricewaterhouseCoopers (PwC) is the world's leading network of audit and assurance firms our clients include almost half of the Fortune 500. Our leading edge audit approach focused on quality is designed to meet the needs of private companies to large organizations. The PwC audit is underpinned by our deep industry knowledge, wide international experience and global network of skilled professional...
Impax Laboratories, Inc. Hayward, CA, 94542
Position Summary: Responsible for the management of third party contract manufacturers and external partners. Assures product is safe, pure and effective. Direct review and inspection of the finished goods and documentation. Ensures that all documentation for release is present, accurate and within established ranges and specifications. Approves or rejects product based on conformance to specific...
Impax Laboratories, Inc. Hayward, CA, 94542
Position Summary: Responsible for the management of third party contract manufacturers and external partners. Assures product is safe, pure and effective. Direct review and inspection of the finished goods and documentation. Ensures that all documentation for release is present, accurate and within established ranges and specifications. Approves or rejects product based on conformance to specific...
Building on its heritage of more than 65 years, Alcon, the global leader in eye care, is the second largest division of the Novartis Group with combined pro-forma sales of more than USD 10 billion in 2013. The division was formed by Novartis on April 8, 2011, following the closing of the merger between Alcon and Novartis. The new Alcon Division combines the product portfolios, commercialization ca...
Building on its heritage of more than 65 years, Alcon, the global leader in eye care, is the second largest division of the Novartis Group with combined pro-forma sales of more than USD 10 billion in 2013. The division was formed by Novartis on April 8, 2011, following the closing of the merger between Alcon and Novartis. The new Alcon Division combines the product portfolios, commercialization ca...
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 ...
Gilead Sciences, Inc. Foster City, CA
Specific Responsibilities: Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. Our worldwide staff of over 6,50...
Agilent Technologies Inc. Santa Rosa, CA, DK
Date Posted: 04/Jul/14 Requisition: 2056076 Job Title: QA Specialist for Product Quality Management Description: We are looking for a QA Specialist in our QA System Department in Dako Denmark with skills and interest in Quality Assurance of In Vitro Diagnostic products. QA System is a part of the Global RA/QA function that has its head office in Denmark and departments in USA, Japan and China. ...
Allergan Irvine, CA
Description JOB SUMMARY: Provides technical expertise in all aspects of product, equipment and process validation including scale-up, new manufacturing site qualifications, new product introductions, sterilization process validation, cleaning validation, preparation of manufacturing and control records and assistance in the preparation of subparts of drug applications. Technical expertise provid...
Allergan Irvine, CA
Description JOB SUMMARY: Supports Allergan, Inc.’s global quality assurance and quality control functions. Ensures that product made at Allergan manufacturing sites and 3rd party contract manufacturing, all in-house and third party support services meet corporate and regulatory requirements. Develops and implements quality systems for Pharmaceuticals and Devices on a global basis. Supports metho...
General Position Summary/Purpose: This position will play an essential role in the company’s Clinical Quality Assurance (CQA) program focused on conducting internal and external Good Clinical Practice (GCP), Good Laboratory Practice (GLP) or Pharmacovigilance (PV) audits to ensure that clinical trials are conducted in compliance with applicable regulations, ICH guidelines, Pharmacyclics procedure...
JOB SUMMARY: Provides technical expertise in all aspects of product, equipment and process validation including scale-up, new manufacturing site qualifications, new product introductions, sterilization process validation, cleaning validation, preparation of manufacturing and control records and assistance in the preparation of subparts of drug applications. Technical expertise provided to all All...
SUMMARY The QA Raw Materials Manager will be responsible for QA oversight for BioMarin (Novato) warehouse activities, to include inspection and disposition of incoming manufacturing materials, review and approval of manufacturing material specifications, supplier change management, material incident investigation program, manufacturing pre-weigh kit approvals, reserve sample program, and rejected...
General Position Summary/Purpose: Performs internal and external GMP and Quality System audits to develop vendor partnership and ensure compliance of audited sites. Provides metrics to management and maintains audit schedule and ensures audits are performed when planned. Tracks audit observations as they relate to the manufacture, analytical testing, and supplier audits of clinical drug substance...
JOB SUMMARY: Supports Allergan, Inc.’s global quality assurance and quality control functions. Ensures that product made at Allergan manufacturing sites and 3rd party contract manufacturing, all in-house and third party support services meet corporate and regulatory requirements. Develops and implements quality systems for Pharmaceuticals and Devices on a global basis. Supports method development...
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 ...

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Biotech Career Tools

Quality Assurance Manager - Pharmaceuticals

Salaries

$48,000.00 - $127,680.00
Typical Salary for Quality Assurance Manager - Pharmaceuticals in California
(50 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Bachelor's
51.5%
Master's
24.2%
Some College Coursework Completed
12.1%
Associates
9.1%
Doctorate
3%
(33 Respondents)
Source: Monster.com Careerbenchmarking Tool

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