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Manager Biotech Quality Control Jobs (NOW HIRING)

Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next ... The Manager, Quality Control is responsible for providing oversight for the GMP testing of cell ...

Manager, Quality Control

Bridgewater, NJ · On-site

$90K - $210K/yr

Create/Review and approve quality control operation procedures * Manage the validation of ... biotech environment * At least 2 years in a managerial role * Prior experience related to method ...

Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next ... The Manager, Quality Control is responsible for providing oversight for the GMP testing of cell ...

The Quality Control (QC) Manager is responsible for leading and managing Quality Control laboratory ... biotech, or related) * Strong working knowledge of cGMPs, FDA regulations, and FDA guidance ...

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 ...

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 ...

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 ...

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 ...

QC Analyst

Chapel Hill, NC · On-site

$33.65 - $36.06/hr

Bachelor's degree in Biology, Microbiology, Biochemistry, Biotechnology, Chemistry, or another related life science field OR * 3+ years of relevant Quality Control, Analytical Development, GMP, 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 ...

QC Inspector

Bothell, WA · On-site

$41K - $66K/yr

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 ...

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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 Jun 29, 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 June 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.
Manager, Quality Control

Full-time

Posted 25 days ago


Key responsibilities

  • Provide Quality Control oversight of all cGMP testing of raw materials, in process, product release, clean utility, and environmental monitoring testing.

  • Review and approve all QC related investigations, including deviations, OOS/OOT, and environmental monitoring investigations, with internal and external laboratories.

  • Manage and develop the professional and technical skills and performance of department members.


PCI Pharma Services rating

6.7

Company rating: 6.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

426th of 521 rated manufacturers


Job description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.


We are PCI.


Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

This position is responsible for the daily QC oversight of PCI's laboratory functions. This includes all operational and technical activities in delivering quality chemical, biopharmaceutical and microbiologic testing services to our customers. This position oversees core activities such as in process testing and micro testing. The role includes oversight of raw material, in process, and reviewing release testing of GMP products to support our clients, interacting with Clients concerning project specific QC issues, approving department cGMP documents, contributing to cGMP reports, and managing QC staff as necessary to achieve these tasks.

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ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Provides Quality Control oversight of all cGMP testing of raw materials, in process, product release, clean utility and environmental monitoring testing. Review and approve all QC related investigations (deviations, OOS/OOT, EM Investigations, etc.) both with internal and external laboratories
  • Maintains good relations and communications with clients as a primary technical interface
  • Interact with customers to identify opportunities to improve quality and establish feedback with manufacturing personnel
  • Interface with supplier and customer quality representatives concerning problems with quality control and assure that effective corrective action is implemented
  • Working with project teams to represent Quality Control, conducting risk assessments and introducing best practices into the Quality Control processes
  • Leading customer interaction on all QC related projects including routine testing updates
  • Manage and develop professional and technical skills and performance of department members
  • Assure all QC functions and testing are being performed according to FDA, EMA, ICH and other international regulations, as deemed necessary
  • Supporting regulatory information requests from customers as it pertains to QC. Supporting Operations, Project Management Staff and Quality Assurance as needed
  • Drive technical troubleshooting, operational improvements, and efficiency improvements while working within cGMP and global regulatory compliance
  • Demonstrate substantial knowledge of subject matter, industry best practices and trends
  • Other tasks as assigned by management.

QUALIFICATIONS:

Required:

  • BS in Chemistry, Biochemistry, Microbiology, Biology or related life sciences field. Advanced level degree preferred
  • 5+ years of Pharmaceutical or Biotechnology industry experience
  • Experience in leading a commercial, aseptic drug product quality control team,
  • 5+ years previous QC management experience
  • Quality leadership experience working on cross-functional teams to harmonize operational, testing and compliance processes
  • Experience in the Management of +5 people

Preferred:

  • Prior experience in a CMO or dealing with CMOs preferred
  • Demonstrates excellent verbal, written, and interpersonal communication skills
  • Demonstrated ability to perform in a fast-paced environment
  • Highly developed leadership capabilities to motivate and inspire teams
  • Independently motivated, detail oriented and good problem-solving ability.
  • Demonstrates a strong customer service orientation with effective follow through
  • Driven to excellence while encouraging others to engage in process improvement and innovation
  • A leader who inspires and motivates, through excellent listening skills and a willingness to mentor team members

#LI-RS1

Join us and be part of building the bridge between life changing therapies and patients. Let's talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.


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