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Qc Biotech Jobs in California (NOW HIRING)

BioPhase Solutions

QC Inspector

San Diego, CA

$18 - $19.80/hr

Quality Control Inspector Are you passionate about ensuring the highest quality standards in the biotech industry? We are seeking a skilled and detail-oriented Quality Control Technician to join our ...

TekWissen LLC

Quality Control Specialist

Vacaville, CA · On-site

$20 - $26/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Specialist II Location: Vacaville, CA, 95688 Duration: 6 Months Job Type: Temporary ...

Bachem Holding AG

Quality Control Scientist

Vista, CA · On-site

$62 - $138/hr

A brief overview The Quality Control Scientist performs laboratory day-today operations, guides and ... Minimum of 3 years' experience in GMP pharma/biotech facility * Experience with Equipment ...

TekWissen LLC

Quality Control Scientist

Vacaville, CA · On-site

$20 - $25/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Associate I / Quality Control Scientist Location: Vacaville, CA - 95688 Duration: 6 ...

TekWissen LLC

Quality Control Analyst

Vacaville, CA · On-site

$20 - $25/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Associate / Quality Control Analyst I Location: Vacaville, CA - 95688 Duration: 6 ...

SaniSure LLC

Quality Control Inspector

Camarillo, CA · On-site

$22 - $24/hr

S. and Europe, we supply global pharmaceutical and biotech companies with the critical tools they ... Job Summary The Quality Control Inspector inspects materials, parts, and products at different ...

BioLegend

Quality Control Supervisor

San Diego, CA · On-site

Bachelor's or Master's Degree in Biology, Immunology or a related Science field * 4 to 6 years of biotech industry experience related to Quality Control * 2 years of experience supervising or leading ...

System One

QC Analyst

Novato, CA · On-site

$28 - $32/hr

Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview Leading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 ...

System One

QC Analyst

Novato, CA · On-site

$28 - $32/hr

Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview Leading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 ...

System One

QC Analyst

Novato, CA · On-site

$28 - $32/hr

Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview Leading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 ...

System One

QC Analyst

Novato, CA · On-site

$28 - $32/hr

Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview Leading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 ...

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All JobsQc Biotech JobsQc Biotech Jobs in California

Qc Biotech information

What is a QC Biotech?

A QC (Quality Control) Biotech professional is responsible for ensuring that biotechnology products, such as pharmaceuticals, vaccines, or biologics, meet strict quality and safety standards. They perform laboratory tests, analyze samples, and document results to ensure compliance with regulatory guidelines. QC Biotech professionals play a crucial role in maintaining the integrity of products before they reach the market, working closely with other departments to resolve any quality issues. Their work helps protect patient safety and supports the success of biotech companies.

What are the key skills and qualifications needed to thrive as a QC Biotech?

To thrive as a QC Biotech, you need a solid background in biology, chemistry, and laboratory techniques, usually supported by a degree in life sciences or a related field. Familiarity with analytical instruments such as HPLC, PCR, and ELISA, as well as GMP regulations and LIMS software, is typically required. Attention to detail, strong problem-solving abilities, and effective teamwork are crucial soft skills for this role. These skills and qualities ensure accurate testing, regulatory compliance, and the integrity of biotechnological products.

What are some common challenges faced by QC Biotech professionals and how can they be addressed?

QC Biotech professionals often encounter challenges such as adapting to rapidly changing regulatory standards, troubleshooting complex assay discrepancies, and maintaining precise documentation under tight deadlines. Addressing these challenges requires continuous learning, strong attention to detail, and effective collaboration with cross-functional teams like R&D and manufacturing. Leveraging robust Standard Operating Procedures and clear communication with colleagues can help ensure consistent results and regulatory compliance.

What is the difference between Qc Biotech vs Qc Microbiologist?

AspectQc BiotechQc Microbiologist
Required CredentialsBachelor's in Biology, Biotechnology, or related field; GMP/GxP trainingBachelor's in Microbiology, Biology, or related; microbiology certifications
Work EnvironmentBiotech manufacturing labs, quality control departmentsMicrobiology labs, pharmaceutical or biotech settings
Employer & Industry UsageBiotech companies, pharmaceutical manufacturersPharmaceutical firms, biotech research labs
Common Search & ComparisonYesYes

While both Qc Biotech and Qc Microbiologist roles involve quality testing in biotech and pharmaceutical settings, Qc Biotech focuses on overall product quality, including assays and validation, whereas Qc Microbiologists specialize in microbiological testing and contamination control. The roles often overlap but differ in specific expertise and focus areas.

What are the most commonly searched types of Qc Biotech jobs in California?

The most popular types of Qc Biotech jobs in California are:

What are popular job titles related to Qc Biotech jobs in California?

For Qc Biotech jobs in California, the most frequently searched job titles are:

What job categories do people searching Qc Biotech jobs in California look for?

The top searched job categories for Qc Biotech jobs in California are:

What cities in California are hiring for Qc Biotech jobs?

Cities in California with the most Qc Biotech job openings:

Qc Biotech jobs near you
Infographic showing various Qc Biotech job openings in California as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 90% Full Time, 5% Part Time, 2% Contract, and 1% Nights. Highlights an 92% Physical, 4% Hybrid, and 4% Remote job distribution.

Senior Manager, Quality Control

Vir Biotechnology

San Francisco, CA • On-site

$142K - $199K/yr

Full-time

Medical, Retirement, PTO

Re-posted 2 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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