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Manager Biotech Quality Control Jobs (NOW HIRING)

Legend Biotech US

Sr. QC Analyst

Raritan, NJ · On-site

$24.50 - $33/hr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Employs good project management principles to appropriately align time, resources, and budgets.

Precigen, Inc

QC Manager

Germantown, MD · On-site

$95K - $120K/yr

Job Title: QC Manager Department: Quality Control - Analytical GENERAL DESCRIPTION: * QC Manger is ... biotech industry under GMP guidelines, with demonstrated expertise in multiple disciplines and ...

Cristcot

Senior Quality Manager

Oversee quality systems including CAPA, deviations, change control, and document management ... pharmaceutical/biotech QA roles, with leadership responsibility * Strong knowledge of cGMP ...

Frontage Laboratories

QC Manager

Exton, PA · On-site

Quality Control (QC) Manager Department: Biomarker & Biologics Location: Exton, PA ( Onsite ... Bachelor's or Master's in Biology, Biochemistry, Immunology, Biotechnology, or related field.

BioPhase Solutions

QC Inspector

San Diego, CA

$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 ...

Bachem

Quality Control Project Manager

Torrance, CA

$98K - $135K/yr

Bachelor's degree in chemistry or a related life sciences field * 5+ years' QC experience in biotech/pharma * 3+ years' experience in a biotech/pharma CDMO setting * 4+ years of project management ...

Granules

Quality Control Manager

Chantilly, VA · On-site

Requires minimum BA/BS in Biochemistry, Chemistry or related field with 10-15 years' experience in the biotech or pharmaceutical industry. Management experience in Quality Control required MS/MA.

Thorne

Manager, Quality Control

Summerville, SC · On-site

Manager, Quality Control Department: Quality Control - Corporate Employment Type: Full Time ... Previous experience in pharmaceutical, biotechnology, dietary supplement, or food manufacturing ...

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All JobsManager Biotech Quality Control Jobs

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:
Manager Biotech Quality Control jobs near you
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.

Sr. QC Analyst

Legend Biotech US

Raritan, NJ • On-site

$24.50 - $33/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago

Key responsibilities

  • Perform QC testing related to the manufacturing of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment.

  • Conduct analytical testing of raw material, utility, in-process, or final product samples submitted to the QC laboratories.

  • Create, review, and approve relevant QC documents, SOPs, and work instructions.

Job description

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.
Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.
Legend Biotech is seeking a Sr. QC Analyst as part of the Quality team based in Raritan, NJ.
Shift: 3rd shift Wed-Sat
Role Overview
The Sr. QC Analyst is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment.
Key Responsibilities
  • Be responsible for the completion of QC testing related to the manufacturing of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment.
  • Ensure testing is completed in compliance with all applicable procedures, standards and GMP regulations.
  • Conduct analytical testing of raw material/utility, in-process, or final product samples submitted to the QC laboratories.
  • Perform peer review/approval of laboratory data.
  • Utilize electronic systems (LIMS) for execution and documentation of testing.
  • Create, review and approve relevant QC documents, SOP's and WI's.
  • Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
  • Work in a collaborative team setting with quality counterparts that include Quality Assurance, Manufacturing Operations, and Analytical/Process Development.
  • Job duties performed require routine exposure to and handling of biological materials and hazardous chemicals.

Requirements
  • Bachelor's Degree in Science, Engineering or equivalent technical discipline is required.
  • Minimum of 1 year relevant work experience, preferably within a biological and/or pharmaceutical industry is required.
  • Experience in a Quality Control setting is preferred.
  • Experience with processing samples in biosafety cabinets utilizing aseptic technique is strongly preferred.
  • Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products is strongly preferred.
  • Knowledge of Good Tissue Practices is required.
  • Knowledge of CAR-T QC test methods and related equipment is preferred.
  • Excellent written and oral communication skill are required.
  • Candidates must be able to accommodate shift schedule. Shifts include routine weekend and evening work as required by the manufacturing process.
  • Candidates must be able to accommodate unplanned overtime (including nights and weekends) on little to no prior notice.
  • The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision.
  • Comfortable with speaking and interacting with regulatory inspectors.
  • This position may require occasional travel to partner sites in NJ or PA as business demands.
  • This position may require up to 5% domestic or international travel as business demands.
  • Takes responsibility for one's results and deliverables; sets and achieves goals to support organizational priorities.
  • Takes initiative; willing to take unpopular positions/actions when necessary; courageous and assertive.
  • Works effectively in the face of ambiguity, shifting priorities, and rapid change; maintains a positive outlook in difficult situations; a change agent.
  • Identifies and focuses on activities of highest value and impact; makes informed decisions quickly.
  • Results oriented; defines goals, metrics and actionable plans and manages work to deliver desired outcomes; has a sense of urgency.
  • Considers resources, alternatives, constraints and desired outcomes to make effective decisions.
  • Employs good project management principles to appropriately align time, resources, and budgets.
  • Appreciates diverse perspectives and is actively inclusive of others' input and ideas; treats others with respect.
  • Articulates ideas clearly and succinctly in a variety of settings and styles; can get messages across that have the desired effect.
  • Leverages personal credibility and interpersonal skills to help others make better decisions and positively impact outcomes; able to develop/maintain effective working relationships internally and externally.
  • Employs a global mindset in decision-making and errs on the side of over-communicating to create organizational transparency, trust and alignment.
  • Takes initiative, actively shares knowledge, builds skills, promotes new ideas and embraces change.
  • Generates new solutions to problems by challenging the status quo and conventional thinking.

#Li-RP1
#Li-Onsite
The base pay range below is what Legend Biotech USA Inc. reasonably expects to offer at the time of posting. Actual compensation may vary based on experience, skills, qualifications, and geographic location. The company reserves the right to modify this range as needed and in accordance with applicable laws.
Other Types of Pay: Performance-based bonus and/or equity is available to employees in eligible roles.
Benefits and Paid Time Off: Medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer eight (8) weeks of paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and eleven (11) company holidays. Additional voluntary benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
Pay Range (Base Pay):
$83,711-$109,870 USD
Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.
EEO Statement
It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances.
Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company.
For information related to our privacy notice, please review: Legend Biotech Privacy Notice.

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