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Biotech Quality Control Jobs (NOW HIRING)

Legend Biotech US

QC Analyst I/II

Raritan, NJ · On-site

$24.50 - $33/hr

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Role Overview The QC Analyst is an exempt level position with responsibilities for performing QC ...

BioPhase Solutions

QC Inspector

San Diego, CA · On-site

$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 ...

LegendBiotech

WI · On-site

$60 - $80/hr

As a QC analyst, you will play a critical role in ensuring the highest quality of life-saving cell ... Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting ...

Legend Biotech USA, Inc.

$24.50 - $33/hr

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Role OverviewThe QC Analyst is an exempt level position with responsibilities for performing QC ...

Legend Biotech USA

QC Analyst I/II

Raritan, NJ · On-site

$60 - $80/hr

Legend Biotech is seeking a QC Analyst as part of the Quality Operations team based in Raritan, NJ. Role Overview The QC Analyst is an exempt level position with responsibilities for performing QC ...

Legend Biotech USA, Inc.

$63K - $83K/yr

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... The QC Specialist is encouraged to work independently on routine tasks and have conceptual ...

Gator Bio

Quality Control Biochemist

Palo Alto, CA

$33 - $35/hr

Gator Bio is a growing biotech company located in Palo Alto, CA. We develop, manufacture and market ... Performing QC testing and validation following written procedures using GMP compliance.

Gator Bio

Quality Control Biochemist

Palo Alto, CA · On-site

$33 - $35/hr

Gator Bio is a growing biotech company located in Palo Alto, CA. We develop, manufacture and market ... Performing QC testing and validation following written procedures using GMP compliance.

Gator Bio

Quality Control Biochemist

Palo Alto, CA · On-site

$33 - $35/hr

Gator Bio is a growing biotech company located in Palo Alto, CA. We develop, manufacture and market ... Performing QC testing and validation following written procedures using GMP compliance.

Ardena

Scientist - Quality Control (QC)

Somerset, NJ · On-site

Ardena supports pharmaceutical and biotechnology companies in bringing innovative, complex ... Quality Control Location: Somerset, New Jersey FLSA Status: Exempt Employment Type: Full-Time ...

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 ...

Califesciences

Quality Control Scientist

Vista, CA · On-site

$60 - $80/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 ...

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Biotech Quality Control information

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$30.5K

$81.3K

$129.5K

How much do biotech quality control jobs pay per year?

As of Sep 9, 2026, the average yearly pay for biotech quality control in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

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 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 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.

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Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $81,324 per year, or $39.1 per hour.

Senior Manager, Quality Control

San Francisco, CA • On-site

Vir Biotechnology
Biotechnology Research and Development • 51 - 200 employees
Learn more about Vir Biotechnologyexternal

$142K - $199K/yr

Full-time

Medical, Retirement, PTO

Re-posted 13 days ago

Key responsibilities

  • Execute and operationalize QC strategy for assigned programs and external testing networks.

  • Manage day-to-day QC operations, including overseeing release and stability testing, review of analytical data, and supporting documentation.

  • Coordinate and oversee vendor performance, external lab activities, and method lifecycle activities.

Job description

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.

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