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Biotech Quality Control Jobs in California (NOW HIRING)

QA/QC Director

Glendale, CA · On-site

$100K - $200K/yr

Qualifications: * 5+ years of experience in pharmaceutical, biotechnology, or related regulated industries. * Minimum of 3-5 years of management experience in QA/QC, or Quality Operations.

QA/QC Director

Glendale, CA · On-site

$100K - $200K/yr

Qualifications: * 5+ years of experience in pharmaceutical, biotechnology, or related regulated industries. * Minimum of 3-5 years of management experience in QA/QC, or Quality Operations.

QA/QC Director

Glendale, CA · On-site

$100K - $200K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Qualifications: * 5+ years of experience in pharmaceutical, biotechnology, or related regulated industries. * Minimum of 3-5 years of management experience in QA/QC, or Quality Operations.

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Associate I / QC Laboratory Associate Location: Vacaville, CA - 95688 Duration: 12 ...

QC Lab Technician

Cerritos, CA · On-site

$20 - $22/hr

Our client is a global biotechnology and aesthetics company specializing in skincare solutions. They are seeking a QC Lab Technician to join their growing team! Title: QC Lab Technician (2 Openings ...

QC DIRECTOR

Rocklin, CA · On-site

$180 - $240/hr

CPC works directly with leaders in the biotechnology and pharmaceutical industries to bring ... CPC is seeking a Director of Quality Control (QC) to fill a full‑time, on‑site role in our ...

QC Analyst I

Vacaville, CA · On-site

$20 - $25/hr

Our client is a leading biotechnology company that combines technological expertise with world ... Job Title: QC Analyst Location: Vacaville, CA Duration: 6 months Job Type: Temporary Position Work ...

Quality Control Technician

Santa Clara, CA · On-site

$22 - $28.25/hr

The job opportunity is for one of our clients specializing in biotechnology product development ... Quality Control Technician Location: Santa Clara, CA - 95054 Duration: 12 Months Job Type:

The job opportunity is for one of our clients specializing in biotechnology product development ... Position: Sr. Quality Control Technician Location: Santa Clara, CA - 95054 Duration: 6 Months Job ...

Chemist Quality Control

Anaheim, CA · On-site

$20 - $38/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Dental insurance The QC Chemist will be responsible for sampling and testing raw materials ... Previous experience working in biotechnology, or research laboratory is preferred * Strong ...

Quality Control Technician

Santa Clara, CA · On-site

$22 - $28.25/hr

The job opportunity is for one of our clients specializing in biotechnology product development ... Quality Control Technician Location: Santa Clara, CA - 95054 Duration: 12 Months Job Type:

Designed of exotic alloys, SVF Flow Controls serves many industries including chemical, biotech ... POSITION SUMMARY : The Quality Control Technician is responsible for ensuring products and ...

QC Analyst (Pharma)

Ventura, CA · On-site

$39 - $41/hr

Perform routine QC laboratory testing using analytical techniques including pH, Osmolality, and FT ... biotechnology, or life sciences laboratory environment preferred. * Knowledge of laboratory ...

Supervisor, Quality Control

El Segundo, CA · On-site

$107K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Experience supervising/managing analytical labs within the biotechnology or pharmaceutical industry ... 211), Quality Control, GMPs, GLP. * Comfortable in a fast-pace company environment with minimal ...

Quality Control Analyst

Thousand Oaks, CA

$34.29 - $72.46/hr

  • Medical

  • Dental

  • Vision

  • Retirement

Support various activities within the QC department. * Key responsibilities are to execute ... Experience in quality operations, biotechnology, pharmaceutical or similar GMP manufacturing ...

New

Showing results 21-40

Biotech Quality Control information

See California salary details

$30.1K

$80.3K

$127.8K

How much do biotech quality control jobs pay per year?

As of Aug 16, 2026, the average yearly pay for biotech quality control in California is $80,259.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,700.00 and $98,700.00 per year, depending on experience, location, and employer.

What does a biotech quality control do?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

What is a biotech quality control?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What are the key skills and qualifications needed to thrive in biotech quality control?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

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

The most popular types of Biotech Quality Control jobs in California are:

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

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

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

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

What cities in California are hiring for Biotech Quality Control jobs?

Cities in California with the most Biotech Quality Control job openings:

Infographic showing various Biotech Quality Control job openings in California as of August 2026, with employment types broken down into 50% Temporary, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $80,259 per year, or $38.6 per hour.

Supervisor, Quality Control Biology

Artiva Biotherapeutics, Inc.

San Diego, CA • On-site

$110K - $135K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago


Job description

About Artiva:
We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate, AlloNK®, is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.
For more information, visit
www.artivabio.com.
Job Summary:
Artiva Biotherapeutics is seeking a skilled and motivated Quality Control Supervisor who will be reporting to the Senior Manager, Quality Control. This individual will supervise the Bio Team and support QC biology testing. The individual will additionally perform routine cGMP release and stability testing of Artiva's products.
Duties/Responsibilities:
  • Write and revise SOPs/Test methods that support Artiva's cell therapy products.
  • Operate and test ELISA, Flow Cytometers, automated cell counters, and other analytical instruments and equipment, as needed.
  • Serve as primary QC Biology point of contact for cross-functional teams including Manufacturing, QA, and Regulatory Affairs for release and investigation activities.
  • Lead training and qualification of Bio team members on equipment use and biological test methods.
  • Support activities for QC equipment IQ/OQ/PQs.
  • Lead and perform routine cGMP release and stability testing of Artiva's products; including biological tests, biochemistry, chemistry-based tests as needed.
  • Lead evaluation of QC systems and/or implementation of system improvements.
  • Perform laboratory investigations and write reports for deviations.
  • Ensure data integrity practices (ALCOA+ principles) are followed by the Bio team; support LIMS/ELN implementation and administration as applicable.
  • Assist in laboratory investigations for Out of Specification results.
  • Assist in biological method qualification and validation as needed.
  • Perform periodic trending of QC testing data; identify adverse trends and initiate CAPAs as appropriate.
  • Perform all work according to company policies, SOPs, and cGMP practices.
  • Planning and scheduling for GMP in-process and release testing.
  • Reviewing biology data and investigating OOS and OOT results.
  • Write technical QC protocols and reports as needed.
  • Assist QC and AD team for analytical qualification and validation, as necessary.
  • Develop an in-depth understanding of NK and CAR-NK products, testing, and safety.
  • Maintain records and databases in accordance with procedures.

Qualifications:
  • Bachelor's degree (BS/BA) in Biology, Biochemistry, Immunology, or a related life science field required.
  • Experience with NK cell or CAR-modified cell therapy products preferred; familiarity with viability, cytotoxicity, identity, and potency assays for cell therapy products.
  • Minimum 8 years of cGMP QC experience in a cell therapy/biotech/pharmaceutical setting is required.
  • At least 1 year of Supervisory or team lead experience is required.
  • Knowledge and experience in supporting cGMP deviations, OOS, etc.
  • Basic knowledge of method transfers, qualifications, and validations; current industry practices; and strong experience with guidance interpretation and application
  • Excellent critical thinking and technical writing skills.
  • Computer skills required to operate Microsoft Word, Project, Visio, and Excel programs.

In addition to a great culture, we offer:
  • A beautiful facility
  • An entrepreneurial, highly collaborative, and innovative environment
  • Comprehensive benefits, including:
  • Medical, Dental, and Vision
  • Group Life Insurance
  • Long Term Disability (LTD)
  • 401(k) Retirement Plan
  • Employee Assistance Program (EAP)
  • Flexible Spending Account (FSA)
  • Paid Time Off (PTO)
  • Company paid holidays, including the year-end holiday week
  • Our recognition program, Bonus.ly, is where you can trade in points earned for things you want.

If all this speaks to you, come join us on our journey!
Base Salary: $ 110,000 - $135,000. Exact compensation may vary based on level, skills and experience.