Pharmaceutical Quality Assurance Manager Jobs in California

206 jobs

Quality Assurance Manager Job Label:SYN-QM-PETCA Are you ready to take the next step in your career with a growing contract sterilization service provider to the medical device, tissue and pharmaceutical industries in Petaluma, California? Whether your resume reads "Quality Engineer," "Senior Quality Engineer," "Assistant Quality Manager," or "Quality Assurance Supervisor" you can, by putting yo...

Real Staffing is looking for a permanent Clinical Compliance Manager to join a highly regarded CRO with a great culture in San Jose, California. Company: This 50 person company focuses on helping pharmaceutical, biotechnology, and medical device companies move a new product from conception to FDA Approval. Role: As a Clinical QA GCP Manager you will manage the internal GCP audit program as wel...

Responsibilities for this role are to ensure compliance with current FDA regulations through operational oversight, internal audits, deviation management, proactive process improvement initiatives and release of commercial product. Ensures quality beyond compliance in decisions of deviations, disposition of batches and approval of GMP documents and policies. Drives timely resolution of issues, fol...

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...

Job Description 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 determi...

Isis Pharmaceuticals, Inc., located in the North San Diego County city of Carlsbad, was founded in 1989 to create advanced, novel medicines to treat complex and challenging diseases. We are the pioneer in the discovery and development of antisense drugs with more than 1300 patents. Isis is a challenging, motivating and rewarding environment designed to foster innovation and scientific excellence....

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...

RESPONSIBILITIES: Develop training plans / training curricula by job type for the site Operations and Quality departments. Create and maintain a system for tracking individual employee training and training records. Coordinate and monitor Supervisors’ and Managers’ proficiency and training in using the tracking tool for monitoring staff training currency. Identify and assess current and future...

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 ...

Design Quality Manager Medical Devices A Design Quality Manager with medical device experience is needed in the great San Francisco, CA area with very strong and growing medical products (devices, pharma, and combination products) company. This position carries promotability to the Director of QA level in the near future and possible further promotions. The position requires experience and prior...

Description: This position is responsible for ensuring compliance of Drug Product manufacturing processes according to cGMP regulations. Also responsible for implementing, maintaining, and monitoring all Quality processes necessary for that assurance. This includes leading skilled people, running the operations according to cGMP regulations, and identifying and implementing business process impro...

Job Description Description: This position is responsible for ensuring compliance of Drug Product manufacturing processes according to cGMP regulations. Also responsible for implementing, maintaining, and monitoring all Quality processes necessary for that assurance. This includes leading skilled people, running the operations according to cGMP regulations, and identifying and implementing busin...

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...

Biologics Development and Production facility is currently seeking a QA Validation Manager with experience in Biopharma. Qualified candidates will:- Develop/maintain validation of equipment and/or processes, cleaning, steaming, shipping, computer and automation systems for biologics production facility- Direct the validation activities to support GMP manufacturing - Provide expertise/guidance on c...

Quality Assurance Manager—Petaluma, CA Direct Hire 95K-120K/year Quality Assurance Manger responsibilities include: Maintain a well-defined administrative system for ensuring the following items and activities are properly regulated: standard operating procedure generation and maintenance, distribution tracking of all quality documents, establishment of proficiency testing program, maintenance...

Org Marketing Statement All over the world, Pfizer colleagues are working together to positively impact health for everyone, everywhere. Each position at Pfizer touches and contributes to the success of our business and our world. That’s why, as one of the global leaders in the biopharmaceutical industry, Pfizer is committed to seeking out inspired new talent who share our core values and mission...

About Human Longevity Inc. Human Longevity Inc. (HLI) is the genomics-based, technology-driven company creating the most comprehensive database of whole genome, phenotype and clinical data.? HLI is developing and applying large scale computing and machine learning to make novel discoveries to revolutionize the practice of medicine.? A privately held company headquartered in San Diego, CA, HLI was...

QA Project Manager-150000019R AbbVie (NYSE:ABBV) is a global, research-based biopharmaceutical company formed in 2013 following separation from Abbott Laboratories.The company's mission is to use its expertise, dedicated people and unique approach to innovation to develop and market advanced therapies that address some of the world's most complex and serious diseases.AbbVie employs approximately ...

Key Responsibilities: Review analytical and/or manufacturing batch record packets and associated documentation to support timely release/disposition of drug product/clinical trial supplies and related documents Review clinical documentation and specifications as applicable Write/review processes, SOPs/procedures and related documents Review and approve analytical/stability protocol, data and r...