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Gmp Manager Jobs in California (NOW HIRING)

SBM Management Services LP

GMP Tech

Santa Ana, CA · On-site

$17.75 - $21.50/hr

GMP Tech Job Overview The GMP Tech will be responsible for keeping assigned areas within GMP in ... Communicate with lead, supervisor, co-workers, managers, and customers in a professional manner

Advanced Cleanroom Solutions

GMP Cleaner

Carlsbad, CA · On-site

$14.50 - $17/hr

Role Description The GMP Cleaner is a part-time, on-site role based in Carlsbad, CA, responsible ... Strong reliability, time management, and ability to work independently and as part of a team in an ...

SBM Management Services LP

GMP Tech

Anaheim, CA · On-site

$17.75 - $21.75/hr

GMP Tech Job Overview The GMP Tech will be responsible for keeping assigned areas within GMP in ... Communicate with lead, supervisor, co-workers, managers, and customers in a professional manner

SBM Management Services LP

GMP Tech

Santa Ana, CA · On-site

$17.75 - $21.50/hr

GMP Tech Job Overview The GMP Tech will be responsible for keeping assigned areas within GMP in ... Communicate with lead, supervisor, co-workers, managers, and customers in a professional manner

SBM Management Services LP

GMP Tech

Garden Grove, CA

$17.25 - $21/hr

GMP Tech Job Overview The GMP Tech will be responsible for keeping assigned areas within GMP in ... Communicate with lead, supervisor, co-workers, managers, and customers in a professional manner

BioLegend

Scientist - Bioassay GMP

San Diego, CA · On-site

Job Summary The primary role of a Bioassay GMP scientist will be to release GMP products through the management of design and development process under current GMP guidelines. Bioassay GMP scientist ...

SBM Management Services LP

GMP Technician

Irvine, CA · On-site

$17 - $18/hr

Title: GMP Technician Job Overview The GMP Tech will be responsible for keeping assigned areas ... Communicate with lead, supervisor, co-workers, managers, and customers in a professional manner

SBM Management Services LP

GMP Technician

Irvine, CA · On-site

$17 - $18/hr

Title: GMP Technician Job Overview The GMP Tech will be responsible for keeping assigned areas ... Communicate with lead, supervisor, co-workers, managers, and customers in a professional manner

SBM Management Services LP

GMP Tech

Irvine, CA · On-site

$18.25 - $22.25/hr

GMP Tech Job Overview The GMP Tech will be responsible for keeping assigned areas within GMP in ... Communicate with lead, supervisor, co-workers, managers, and customers in a professional manner

SBM Management Services LP

GMP Lead

Menlo Park, CA · On-site

$20/hr

GMP Lead Job Overview The GMP Lead will be responsible for overseeing activities within the ... Management Services, LP and its affiliates are proud to be equal opportunity workplaces. We are ...

SBM Management Services LP

GMP Lead

Menlo Park, CA · On-site

$19 - $20/hr

GMP Lead Job Overview The GMP Lead will be responsible for overseeing activities within the ... Management Services, LP and its affiliates are proud to be equal opportunity workplaces. We are ...

Cellares

Director, GMP Systems

South San Francisco, CA · On-site

$90K - $250K/yr

Operational ownership and execution oversight for business-critical and GMP-impacting systems such as: ERP, Manufacturing Execution & Automation Interfaces, Quality Management Systems (QMS), PLM ...

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Gmp Manager information

See California salary details

$24.2K

$58.7K

$114.5K

How much do gmp manager jobs pay per year?

As of Aug 21, 2026, the average yearly pay for gmp manager in California is $58,746.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,400.00 and $67,600.00 per year, depending on experience, location, and employer.

What is a GMP manager?

GMP Managers are professionals responsible for ensuring that manufacturing processes in industries such as pharmaceuticals, biotechnology, and food production comply with Good Manufacturing Practice (GMP) regulations. They oversee quality control, develop and implement standard operating procedures, and conduct internal audits to maintain regulatory standards. Their role is crucial for ensuring that products are consistently produced and controlled according to quality standards, thereby safeguarding consumer health and safety.

What are some common challenges faced by a GMP manager in maintaining regulatory compliance, and how are they typically addressed?

A GMP Manager often encounters challenges such as keeping up with evolving regulatory standards, ensuring consistent staff training, and managing thorough documentation. To address these, managers implement regular training programs, conduct internal audits to identify gaps, and foster a culture of quality across teams. Staying proactive about changes in regulations and collaborating with cross-functional teams helps ensure ongoing compliance and smooth inspections.

What are the key skills and qualifications needed to thrive as a GMP manager, and why are they important?

To thrive as a GMP Manager, you need in-depth knowledge of Good Manufacturing Practices, quality assurance, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with quality management systems (QMS), audit tools, and relevant certifications such as Six Sigma or ISO standards is typically required. Strong leadership, problem-solving abilities, and effective communication are vital soft skills for managing teams and ensuring adherence to regulations. These skills and qualifications ensure product safety, regulatory compliance, and continuous improvement within manufacturing processes.

What is the difference between Gmp Manager vs Quality Assurance Manager?

AspectGmp ManagerQuality Assurance Manager
CertificationsGMP certifications, Quality Management certificationsISO 9001, Quality Management certifications
Work EnvironmentPharmaceutical, biotech, or medical device manufacturingVarious industries including manufacturing, healthcare, and food
Employer & Industry UsageRegulated industries with strict compliance standardsBroadly used across multiple industries for quality oversight
Primary FocusEnsuring compliance with Good Manufacturing PracticesOverseeing overall quality assurance processes

The Gmp Manager primarily focuses on ensuring compliance with Good Manufacturing Practices in regulated industries like pharmaceuticals and biotech. In contrast, the Quality Assurance Manager oversees broader quality assurance processes across various industries. Both roles require similar certifications and work environments but differ in their specific compliance and quality scope.

What are popular job titles related to Gmp Manager jobs in California?

For Gmp Manager jobs in California, the most frequently searched job titles are:

What job categories do people searching Gmp Manager jobs in California look for?

The top searched job categories for Gmp Manager jobs in California are:

What cities in California are hiring for Gmp Manager jobs?

Cities in California with the most Gmp Manager job openings:

Gmp Manager jobs near you
Infographic showing various Gmp Manager job openings in California as of August 2026, with employment types broken down into 90% Full Time, 9% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $58,746 per year, or $28.2 per hour.

Senior Manager, GMP Quality

Revolution Medicines

Redwood City, CA • Hybrid

Full-time

Re-posted 18 days ago

Job description

The Opportunity:

Revolution Medicines is seeking a Senior Manager, GMP Quality who will play a key role within Quality Assurance and is responsible for providing leadership and operational GMP QA support for RevMed clinical programs, with a primary focus on clinical batch record review, product disposition, and release activities supporting global clinical trials.

Responsibilities:

  • Serve as the primary QA lead for clinical batch disposition activities, including comprehensive review and approval of executed batch records, deviations, investigations, and associated release documentation to ensure timely disposition of clinical trial materials.

  • Provide QA support for the manufacture, packaging, labeling, testing, storage, and release of clinical drug substance (DS), drug product (DP), and final product (FP) manufactured at CMOs and other GMP service providers.

  • Partner cross-functionally with Pharmaceutical Development & Manufacturing (PDM/CMC), Supply Chain, Regulatory Affairs, Clinical Operations, Analytical Development, and external CMOs to support uninterrupted supply of clinical trial materials.

  • Review and approve GMP documentation associated with clinical manufacturing and release activities, including master batch records, executed batch records, specifications, Certificates of Analysis, stability data, label proofs, shipping documentation, and analytical test results.

  • Collaborate with internal and external stakeholders to support quality systems and serve as QA SME for deviation investigations, CAPAs, change controls, product impact assessments, shelf-life extensions, and other GMP quality processes impacting clinical supply.

  • Ensure compliance with applicable global GMP regulations, ICH guidelines, company procedures, and industry best practices related to clinical manufacturing and release activities.

  • Support QA oversight of clinical manufacturing campaigns at CMOs, including on-site or remote support for manufacturing operations, batch review, and disposition activities as needed.

  • Drive continuous improvement initiatives to enhance batch review efficiency, release timelines, and overall effectiveness of GMP quality systems supporting clinical operations.

  • Review and approve GMP SOPs, work instructions, and controlled documents to ensure alignment with current regulatory expectations and company practices.

  • Support quality review of regulatory submissions and responses, including INDs/IMPDs and other clinical regulatory filings, as applicable.

  • Build positive professional relationships and foster a culture of quality, collaboration, accountability, and continuous improvement across internal teams and external partners.

Required Skills, Experience and Education:

  • A Bachelor's degree in a scientific or technical discipline is required.

  • A minimum of 8 years of experience in GMP Quality in the pharmaceutical industry, with experience in early to late-stage drug product development.

  • Excellent analytical skills and a strong technical background in small molecule process development, and testing are strongly desired.

  • Knowledge of applicable US and Global compliance regulations and industry practices.

  • Ability to critically evaluate and troubleshoot complex problems with diligence.

  • Strong teamwork, collaboration, and management skills.

  • Ability to manage multiple priorities and aggressive timelines.

  • Highly responsible, self-motivated professional with enthusiasm and passion for the work.

  • Highly proficient with various Microsoft and other computerized systems (e.g., Word, Outlook, Excel, PowerPoint, Visio, etc.).

Preferred Skills:

  • Hands-on experience working in a manufacturing environment overseeing QA responsibilities for commercial and late-stage programs is preferred. 

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