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Manager Biotech Quality Control Jobs (NOW HIRING)

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that ... Our client is a leading biotechnology company that combines technological insight with world-class ...

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that ... Our client is a leading biotechnology company that combines technological insight with world-class ...

This position reports into the Sr. Quality Manager which is part of Quality organization and ... Minimum Experience : 3-5 years quality-related experience in biotech, the pharmaceutical or ...

This position reports into the Sr. Quality Manager which is part of Quality organization and ... Minimum Experience : 3-5 years quality-related experience in biotech, the pharmaceutical or ...

The Director, Quality Control will provide strategic leadership in managing a growing team of ... Who is Omeros? Omeros is an innovative biotechnology company that discovers, develops, and ...

QC, Analyst I

Raritan, NJ · On-site

$24.50 - $33/hr

Legend Biotech is seeking a QC Analyst I (IPL) as part of the Quality Operations team based in ... Employs good project management principles to appropriately align time, resources, and budgets.

Make recommendations to upper management to acquire more equipment. * Comply with ISO policies and ... 6 years of biotech industry experience related to Quality Control * 2 years of experience ...

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Quality Control Manager

Lumberton, NC · On-site

$100K - $115K/yr

Job Summary We're looking for a hands‐on Quality Control Manager to lead inspection activities for assembled basket strainers, cones, and fabricated components. This role oversees the quality team ...

QC Manager

Charleston, SC · On-site

$125K/yr

Description The Manager of Quality Control is responsible for providing strategic leadership ... Previous experience in nutraceutical, pharmaceutical, biotechnology, dietary supplement, or food ...

QC Manager

Charleston, SC · On-site

$125K/yr

Description The Manager of Quality Control is responsible for providing strategic leadership ... Previous experience in nutraceutical, pharmaceutical, biotechnology, dietary supplement, or food ...

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Showing results 1-20

Manager Biotech Quality Control information

See salary details

$30.5K

$81.3K

$129.5K

How much do manager biotech quality control jobs pay per year?

As of Jul 22, 2026, the average yearly pay for manager 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 the difference between Manager Biotech Quality Control vs Quality Control Specialist?

AspectManager Biotech Quality ControlQuality Control Specialist
CredentialsBachelor's/Master's in Life Sciences, Quality Certifications (e.g., CQE)Bachelor's in Life Sciences or related field, Quality Certifications preferred
Work EnvironmentOversees QC teams, manages testing processes, and ensures compliancePerforms testing, data analysis, and reports results
Employer & Industry UsageBiotech companies, pharmaceutical firms, contract labsBiotech, pharma, and manufacturing sectors

The Manager Biotech Quality Control typically oversees testing teams and ensures compliance with quality standards, while the Quality Control Specialist focuses on executing tests and analyzing data. Both roles require relevant scientific credentials, but the manager has additional responsibilities in team leadership and process management.

What does a Manager Biotech Quality Control do?

A Manager Biotech Quality Control oversees the quality assurance processes within a biotechnology company, ensuring that products meet regulatory standards and internal specifications. They manage teams responsible for testing raw materials, in-process samples, and finished products, and analyze data to identify trends or issues. This role also involves setting quality control policies, training staff, and liaising with regulatory bodies to maintain compliance. Managers in this field play a crucial role in product safety and efficacy, directly impacting the success of biotech products in the market.

What are the most common challenges faced by a Manager in Biotech Quality Control, and how are they typically addressed?

Managers in Biotech Quality Control often face challenges such as ensuring regulatory compliance, maintaining rigorous documentation, and managing a team with diverse expertise. Keeping up-to-date with changing industry standards and regulatory requirements is crucial, as is fostering a culture of continuous improvement and clear communication. These challenges are typically addressed through ongoing staff training, implementing robust quality management systems, and close collaboration with other departments like R&D and manufacturing to ensure that quality standards are consistently met.

What are the key skills and qualifications needed to thrive as a Manager Biotech Quality Control, and why are they important?

To thrive as a Manager Biotech Quality Control, you need a strong background in biology or chemistry, extensive knowledge of quality assurance regulations, and typically a bachelor’s or master’s degree in a life science field. Familiarity with laboratory information management systems (LIMS), GMP (Good Manufacturing Practices), and certifications such as ASQ or Six Sigma are highly valued. Leadership, attention to detail, and strong problem-solving and communication skills help you guide teams and ensure compliance. These skills and qualities are critical for maintaining product quality, regulatory adherence, and the overall success of biotech manufacturing operations.
More about Manager Biotech Quality Control jobs
What cities are hiring for Manager Biotech Quality Control jobs? Cities with the most Manager Biotech Quality Control job openings:
What are the most commonly searched types of Biotech Quality Control jobs? The most popular types of Biotech Quality Control jobs are:
What states have the most Manager Biotech Quality Control jobs? States with the most job openings for Manager Biotech Quality Control jobs include:
What job categories do people searching Manager Biotech Quality Control jobs look for? The top searched job categories for Manager Biotech Quality Control jobs are:
Infographic showing various Manager Biotech Quality Control job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 90% Full Time, 1% Part Time, 1% Temporary, and 6% Contract. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.
Quality Control Scientist

Quality Control Scientist

TekWissen LLC

Vacaville, CA • On-site

$20 - $25/hr

Temporary

Re-posted 24 days ago


Job description

Overview:  

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.   Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.  

Job Title:       QC Associate I / Quality Control Scientist
Location:       Vacaville, CA - 95688
Duration:       6 Months
Job Type:       Temporary Assignment     
Work Type:   Onsite

Summary
 
With limited supervision, the QC Associate I / Quality Control Scientist is responsible for performing direct materials testing in compliance with cGMP regulations. The role involves executing laboratory testing, reviewing and trending data, supporting investigations (OOS, OOT, OOE), and contributing to laboratory operations and quality objectives. The position works closely with Quality Control leadership to meet departmental and organizational goals.

Responsibilities

  • Perform basic to moderately complex laboratory testing in compliance with GMP requirements
  • Review, analyze, and assess test data against established acceptance criteria
  • Conduct technical review of peer-generated data
  • Perform trend analysis and assist in establishing limits
  • Identify discrepancies and support quality investigations and CAPA initiatives
  • Troubleshoot technical and testing-related issues
  • Identify gaps in systems, procedures, and laboratory practices
  • Participate in assay transfer, assay validation, and method-related activities
  • Perform equipment qualification, calibration, and routine maintenance
  • Prepare and maintain standards, controls, stocks, cultures, and reagents per procedures
  • Ensure GMP compliance across laboratory operations
  • Support internal and external audits and regulatory inspections
  • Coordinate with internal customers to support multi-site operations
  • Meet assigned schedules, timelines, and deadlines (95% on-time performance expectation)
  • Participate in or lead team projects, process improvements, and continuous improvement initiatives
  • Write protocols, reports, and technical documentation under limited supervision
  • Provide and receive training as required
  • Perform additional duties as assigned to support Quality activities
Required Skills
  • Bachelor’s degree (B.S./B.A.) in a relevant scientific discipline with 1–3 years of industry experience OR
  • Master’s degree with at least 1 year of relevant experience
  • Experience in the pharmaceutical or biopharmaceutical industry
  • Hands-on experience with analytical and/or biological testing procedures
  • Strong understanding of cGMP regulations and quality systems
  • Experience with OOS, OOT, and OOE investigations
  • Exposure to assay transfer, assay validation, and method lifecycle activities
  • Experience supporting regulatory inspections (FDA, EMA, etc.)
  • Familiarity with trend analysis and data integrity practices
  • Prior involvement in process improvement or cross-functional projects
  • Experience working in multi-site or global operational environments
  • Ability to apply scientific principles, theories, and techniques in a QC environment
  • Strong verbal and written communication skills
  • Sound judgment, analytical thinking, and problem-solving abilities
  • Ability to work independently with limited supervision and manage short-term priorities
TekWissen® Group is an equal opportunity employer supporting workforce diversity.

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 


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About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

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