Pharmaceutical Quality Assurance Manager Jobs in California

218 jobs

Our industry leading Pharmaceutical manufacturing client is seeking a highly motivated and energetic Senior Manager of Quality Assurance Operations. The Senior Manager of Quality Assurance Operations will be a strategic leader in a cross functional management team. This position will work directly with internal and CMO operating units to ensure that commercial drug product operations meet all requ...

Summary of Essential Job Functions - Performs environmental monitoring of control rooms - Performs personnel monitoring of Production Operators - Monitoring of Compounding and Filling Operations, Performing volume checks - Review of Production Records - Conducts releasing inspection of printed roll-stock, labels, inserts and cartons using statistical sampling plans to determine the acceptabil...

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Job Description: The job requires a very versatile individual who can both interact with customer quality managers and work hands on in a product inspection and secondary manufacturing operation environment. There are two primary job responsibilities. The first aspect of the job is to manage the company’s Quality Assurance including taking lead on administering the company’s Quality Management Sy...

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...

Kelly Scientific has a Quality Associate opening with a leading Pharmaceutical company in Irvine, CA. Responsibilities 1. Support the implementation and maintenance of an efficient system for reviewing and releasing finished product. 2. Provide support for the QA Complaint system for all product lines. Duties include the receipt and Investigation of complaints, correspondence with internal/exte...

Irvine Pharmaceutical Services, Inc., is a privately held, premier pharmaceutical development organization supporting the pharmaceutical, biopharmaceutical, and medical device industries. Together with its wholly owned parenteral manufacturing subsidiary, Avrio Biopharma, Irvine offers cGMP contract development and manufacturing support including formulation, analytical development, aseptic fill a...

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...

Johnson & Johnson companies are equal opportunity employers. QUALITY ASSURANCE MANAGER - PLANT QUALITY-8670150220 Description Neutrogena Corporation, a member of Johnson & Johnson's Family of Companies, is recruiting for a QA Manager, Plant Quality to be located in Los Angeles, CA. Neutrogena Corporation develops, manufactures and markets premium skin and hair care products sold worldwide and ...

Dako North America, an Agilent Technologies Company Location: Carpinteria, CA We are searching for an experienced Quality Assurance Manager to work within the Design Assurance team of Dako North America, an Agilent Technologies company. Reporting to the Sr. Director, RA/QA/CA, the successful candidate must have quality assurance experience working in IVD, Medical Devices or Pharmaceutical, with a ...

Overview Responsible for performing Quality activities to ensure compliance with internal and external regulations and procedures. This position provides Quality support for the company’s pharmaceutical products. Responsibilities Essential Duties and Responsibilities Participates in the development, implementation, and maintenance of the company’s quality management system and facilitates cont...

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...

At Agensys, we're changing tomorrow by moving oncology forward. We've developed a pipeline of novel therapeutic fully human monoclonal antibodies (MAbs) to treat solid tumors based on our own proprietary targets. We have discovered and validated a portfolio of clinically relevant targets in 14 different cancer types. Our pipeline includes therapeutic MAbs to multiple cancer indications that are at...

Company Overview Relypsa, Inc. is a late clinical-stage pharmaceutical company leading the discovery and development of novel non-absorbed polymeric drugs for important applications in cardiovascular and renal diseases. Relypsa's lead product candidate is patiromer, a non-absorbed potassium binder, which is being developed for the treatment of hyperkalemia. The company was formed in 2007 and is b...

Manages all plant units responsible for monitoring and ensuring plant products are safe and meet customer specifications and company quality and reliability standards. Develops and implements short-term and mid-term business plans for department, and assists in the development of the strategic plan for the plant. Manages and directs staff responsible for microbiological testing and other quality ...

JOB SUMMARY: Reporting to the Sr Director of QA, this individual will be responsible for oversight of all quality aspects related to manufacture of commercial & clinical products at contract manufacturing organizations (CMOs). In partnership with QC, Regulatory Affairs, Technical Staff and Alliance Management the QA Manager/Associate Director will ensure that products are manufactured in accordanc...

Company Overview Relypsa, Inc. is a late clinical-stage pharmaceutical company leading the discovery and development of novel non-absorbed polymeric drugs for important applications in cardiovascular and renal diseases. Relypsa's lead product candidate is patiromer, a non-absorbed potassium binder, which is being developed for the treatment of hyperkalemia. The company was formed in 2007 and is b...

The Sr. Project Manager, Pharmaceutical Project Management (PM) leads the preparation and execution of project plans for multi-million dollar New Product Development projects, and assists with the development and continuous improvement of standard work for project management.The PM manages global cross-functional team resources throughout the project life cycle, and is accountable for meeting the ...

The Sr. Project Manager, Pharmaceutical Project Management (PM) leads the preparation and execution of project plans for multi-million dollar New Product Development projects, and assists with the development and continuous improvement of standard work for project management. The PM manages global cross-functional team resources throughout the project life cycle, and is accountable for meeting the...

Quality Systems Manager / Auditor This position has the responsibility for all aspects of quality system and compliance. Must be able to support CAPA, Document Control, Records Control, Training and Audits. Assess company activities to assure that the company has an adequate quality system that will comply with the established requirements of federal and international quality system standards (IS...

Title of Job: QA Manager Role Located in : Okta Headquarters (San Francisco, CA) Reports to : Director of Quality Company Description: Okta is an integrated identity and mobility management service. Built from the ground up in the cloud, Okta securely and simply connects people to their applications from any device, anywhere, at anytime. Okta integrates with existing directories and identity sy...