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Quality Control Stability Manager Jobs in California

Quality Control Manager

San Diego, CA · On-site

$35 - $45/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Type Full-time Description As a Construction Quality Control Manager (QCM), your construction expertise and excellent organizational skills will be crucial in ensuring our projects meet or ...

Quality Control Manager

San Diego, CA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Control Manager This role leads the quality control program for federal and military construction projects, ensuring all work meets contract requirements, project specifications, and ...

Quality Control Manager

San Diego, CA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Control Manager This role leads the quality control program for federal and military construction projects, ensuring all work meets contract requirements, project specifications, and ...

Quality Control Manager

Los Angeles, CA · On-site

$113K - $125K/yr

Quality Control (QC) Manager Project Duration: October 1, 2026 - August 31, 2028 Position Summary The Quality Control Manager oversees all quality assurance and quality control activities for airport ...

Quality Control Manager

San Carlos, CA · On-site

$95K - $195K/yr

  • Medical

  • Life

  • Retirement

  • PTO

Quality Control Manager (Inspection Team) Joby Aviation is seeking a Quality Control Manager to lead shop-floor Quality Control and Inspection teams across manufacturing operations. Reporting to the ...

Quality Control Manager

San Carlos, CA · On-site

$95K - $195K/yr

  • Medical

  • Life

  • Retirement

  • PTO

Overview Quality Control Manager (Inspection Team) Joby Aviation is seeking a Quality Control Manager to lead shop-floor Quality Control and Inspection teams across manufacturing operations.

Quality Control Manager

San Carlos, CA

$95K - $195K/yr

  • Medical

  • Life

  • Retirement

  • PTO

Overview Quality Control Manager (Inspection Team)Joby Aviation is seeking a Quality Control Manager to lead shop-floor Quality Control and Inspection teams across manufacturing operations. Reporting ...

Manager, Quality Control - Analytical

Newark, CA · Hybrid

$140K - $150K/yr

  • Medical

  • Life

  • Retirement

  • PTO

... product release, stability, method lifecycle management, and ensure laboratory readiness for ... Lead QC analytical testing activities supporting clinical and commercial DS and DP manufacturing ...

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Quality Control Manager

San Diego, CA · On-site

$80K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Capital Brand Group, LLC (CBG) is hiring a Quality Control Manager to own the quality of all work performed under our federal Building Maintenance & Operations contract with U.S. Customs and Border ...

Quality Control Manager

Napa, CA · On-site

  • Medical

  • Retirement

Implement and manage Quality Control Program per contract specifications and project QC Plan. Requirements : * Work closely with the Project Superintendent and Project Manager coordinating quality ...

Quality Control Manager

Napa, CA · On-site

  • Medical

  • Retirement

Implement and manage Quality Control Program per contract specifications and project QC Plan. Requirements : * Work closely with the Project Superintendent and Project Manager coordinating quality ...

Quality Control Manager

Los Angeles, CA

$115K - $160K/yr

  • Medical

  • Retirement

  • PTO

The Quality Control Manager will provide management and oversight for the overall QC processes and serve as the primary point of contact for clients, design teams, field staff, and subcontractors ...

Manager Quality Control

Upland, CA · On-site

$90K - $115K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are looking for a Manager of Quality Control Field who is passionate about building "boots on the ground" excellence and mentoring the next generation of industry experts. Join a team that ...

Showing results 21-40

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Senior Manager, Quality Control

Vir Biotechnology

San Francisco, CA • On-site

$142K - $199K/yr

Full-time

Medical, Retirement, PTO

Re-posted 23 days ago


Job description

Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN® dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.
Vir Biotechnology has exclusive rights to the universal PRO-XTEN® masking platform for oncology and infectious disease. PRO-XTEN® is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.
We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.
THE OPPORTUNITY
The Senior Manager, Technical Operations Quality Control, is responsible for executing and operationalizing QC strategy across assigned programs and external testing partners (e.g., CDMOs/CTLs) from Phase 1 through commercialization. This role ensures the timely and compliant delivery of QC activities, including release and stability testing, method lifecycle management, and vendor oversight.
The Senior Manager partners cross-functionally with Quality, Technical Operations, Regulatory, and Analytical Development to deliver program milestones, maintain inspection readiness, and support global regulatory submissions. This individual contributes to the development of QC strategy and drives continuous improvement in QC processes, systems, and external network performance.
This role is located in our San Francisco headquarters with an expectation of 3 days per week in office.
WHAT YOU'LL DO
  • Execute and operationalize QC strategy for assigned programs and external testing networks in alignment with QC and Quality organization strategy.
  • Lead QC activities across the product lifecycle (Phase 1 through commercial) for designated programs, ensuring effective implementation of phase-appropriate control strategies.
  • Support development and refinement of QC strategies, including methods, specifications, and testing approaches, in collaboration with Analytical Development and QC leadership.
  • Drive consistent execution and harmonization of QC methods, specifications, and practices across programs and external partners.
  • Identify, assess, and escalate risks to QC performance, supply continuity, and compliance, and implement mitigation plans with cross-functional stakeholders.
  • Represent QC on program teams and sub-teams, ensuring alignment of analytical deliverables, timelines, and QC readiness for key CMC milestones.
  • Manage day-to-day execution of QC operations to ensure timely, compliant testing for clinical and commercial programs.
  • Coordinate and oversee release and stability testing (including CDMOs/CTLs), including review of analytical data, batch records, and supporting documentation; support CoA generation.
  • Lead execution of QC GMP processes (deviations, OOS/OOT, change controls, investigations) in collaboration with QA.
  • Coordinate QC documentation and logistics at external labs, including sampling plans, shipments, and reagent/inventory management.
  • Manage vendor performance and execution, including CTL/CDMO oversight and routine operational interactions.
  • Execute method lifecycle activities (qualification, transfer, validation, implementation, and monitoring) across internal and external labs.

WHO YOU ARE AND WHAT YOU BRING
  • BA/BS with 10 + years experience, MA/MS/MBA with 8+ years experience in Biochemistry, Chemistry, Biology, Virology, Chemical Engineering or a related discipline is preferred
  • Technical expertise in a wide range of analytical methods for release and stability testing of monoclonal antibodies
  • Strong scientific background in Quality Control and/or assay development in biotech industry with strong knowledge of cGMP/ICH/FDA/EMA regulations
  • Expertise with analytical test method optimization, validation, and transfer as well as working with contract organizations

#LI-AS1
#LI-Onsite
WHO WE ARE AND WHAT WE OFFER
The expected salary range for this position is $142,500 to $199,000 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.
Vir Biotechnology's compensation and benefits are aligned with the current market and commensurate with the person's experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.
Applicants must currently be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.
This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs. Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.
Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.
For hires based in the United States, Vir Biotechnology, participates in E-Verify.
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