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Manager Qc Biotech Jobs (NOW HIRING)

BridgeBio Pharma

Manager, Quality Control

$144K - $159K/yr

... a "moneyball for biotech" approach, pooling projects and promising early-stage research from ... What You'll Do The Quality Control Manager is responsible for ensuring that all activities ...

TransMedics

Manager Quality Control

Andover, MA · On-site

Overall management of quality control activities; oversee the development and implementation of robust systems and procedures to ensure evaluation, measurement and improvement of processes. * Manage ...

Kop-Coat, Inc.

Mgr/Quality Control

Attleboro, MA

The primary result expected from the Quality Manager will be to formulate quality control policies and control quality of laboratory and production efforts by planning, directing, and coordinating ...

New

Newrez

Manager - Quality Control

Bethel Park, PA

The QC Manager plays a key leadership role in developing quality strategies, managing staff, and continuously improving appraisal review processes to maintain integrity and customer confidence.

Newrez LLC

Manager - Quality Control

Bethel Park, PA · On-site

The QC Manager plays a key leadership role in developing quality strategies, managing staff, and continuously improving appraisal review processes to maintain integrity and customer confidence.

Rust-Oleum

Mgr/Quality Control

Attleboro, MA

The primary result expected from the Quality Manager will be to formulate quality control policies and control quality of laboratory and production efforts by planning, directing, and coordinating ...

New

MSD

Manager, Quality Control

West Point, PA · On-site

The Quality Control Manager provides quality oversight of the qualified utilities and facility environmental monitoring sampling at the West Point vaccine manufacturing site. The Manager, with ...

Rust-Oleum

Mgr/Quality Control

Attleboro, MA · On-site

The primary result expected from the Quality Manager will be to formulate quality control policies and control quality of laboratory and production efforts by planning, directing, and coordinating ...

New

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Manager Qc Biotech information

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$81.3K

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How much do manager qc biotech jobs pay per year?

As of Aug 31, 2026, the average yearly pay for manager qc biotech 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 does a manager QC Biotech do?

A Manager QC (Quality Control) Biotech oversees the quality control processes in a biotechnology organization. They are responsible for managing teams that conduct laboratory testing, ensuring products meet regulatory standards, and developing protocols to maintain high-quality results. Their role involves coordinating with other departments, reviewing data, troubleshooting issues, and ensuring compliance with industry regulations such as GMP (Good Manufacturing Practice). Ultimately, they play a crucial part in guaranteeing the safety and effectiveness of biotech products before they reach the market.

What are some typical challenges a manager QC Biotech might face when overseeing quality control in a fast-paced biotech environment?

A Manager QC Biotech often encounters challenges such as maintaining compliance with evolving regulatory standards, managing tight timelines for product release, and ensuring consistent data integrity across multiple projects. Coordinating with cross-functional teams, such as manufacturing and R&D, requires strong communication skills to address unexpected quality issues promptly. Additionally, implementing new technologies and training staff on updated protocols while minimizing disruptions can be demanding but is crucial for continuous improvement and success in the role.

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

To thrive as a Manager QC Biotech, you need a solid background in life sciences, quality control principles, and regulatory compliance, often supported by a relevant degree and experience in biotech or pharmaceutical environments. Familiarity with laboratory information management systems (LIMS), GMP regulations, and analytical instrumentation is crucial. Strong leadership, problem-solving, and communication skills help manage teams and coordinate with cross-functional departments. These skills are vital to ensure product quality, regulatory adherence, and efficient team operations in a highly regulated industry.
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Manager Qc Biotech jobs near you
Infographic showing various Manager Qc Biotech job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.

Senior Manager, Quality Control

Vir Biotechnology

San Francisco, CA • On-site

$142K - $199K/yr

Full-time

Medical, Retirement, PTO

Re-posted 5 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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