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Biotechnology Quality Control Analyst Jobs (NOW HIRING)

$24.50 - $33/hr

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

QC Analyst I

Sellersville, PA · On-site

$23.25 - $31.25/hr

The QC Analyst I will support laboratory operations through accurate testing, documentation ... Experience in pharmaceutical, biotechnology, or other regulated laboratory environments.

QC Analyst I

Sellersville, PA · On-site

$23.25 - $31.25/hr

The QC Analyst I will support laboratory operations through accurate testing, documentation ... Experience in pharmaceutical, biotechnology, or other regulated laboratory environments.

Quality Control Analyst

Charlotte, NC · On-site

$22.50 - $30/hr

Quality Control Analyst Candidates shall work to support requirements for PR0001 Program Support and will review and analyze the curriculum and substance of in-person, Webinar, and small group ...

QC Analyst IV

Portsmouth, NH · On-site

$24.50 - $32.75/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Analyst IV Location: Portsmouth, NH 03801 Duration: 8 Months Job Type: Temporary ...

QC Analyst I/II

Raritan, NJ · On-site

$24.50 - $33/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 ...

Quality Control Analyst II

Rensselaer, NY · On-site

$23.75 - $32/hr

Quality Control Analyst II in Rensselaer, NY - Nights Build your future at Curia, where our work ... biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to ...

Quality Control Analyst II

Rensselaer, NY · On-site

$23.75 - $32/hr

Quality Control Analyst II in Rensselaer, NY - Nights Build your future at Curia, where our work ... biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to ...

Quality Control Analyst II

Rensselaer, NY · On-site

$23.75 - $32/hr

Quality Control Analyst II in Rensselaer, NY - Nights Build your future at Curia, where our work ... biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to ...

Quality Control Analyst II

Rensselaer, NY · On-site

$23.75 - $32/hr

Quality Control Analyst II in Rensselaer, NY - Nights Build your future at Curia, where our work ... biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to ...

QC Analyst (Pharma)

Ventura, CA · On-site

$39 - $41/hr

Perform routine QC laboratory testing using analytical techniques including pH, Osmolality, and FT ... biotechnology, or life sciences laboratory environment preferred. * Knowledge of laboratory ...

QC Analyst I/II

Raritan, NJ · On-site

$24.50 - $33/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 ...

New

Quality Control Analyst

Smithfield, PA · On-site

$24.50 - $32.75/hr

Quality Control Analyst Location: Smithfield, PA At Johnson Matthey, your work will matter. As a Quality Control Analyst,you'lljoin a world leader in platinum group metals with over 200 years of ...

Quality Control Analyst

Smithfield, PA · On-site

$24.50 - $32.75/hr

Quality Control Analyst Job title: Quality Control Analyst Location: Smithfield, PA At Johnson Matthey, your work will matter. As a Quality Control Analyst, you'll join a world leader in platinum ...

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 ...

New

QC Analyst III

Portsmouth, NH · On-site

$25 - $30/hr

Our client is a leading biotechnology company that combines technological expertise with world ... Job Title: QC Analyst III Location: Portsmouth, NH 03801 Duration: 12 months Job Type: Temporary ...

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Quality Control Analyst

Memphis, TN · On-site

$20.13 - $21.13/hr

The Quality Control Analyst I for the QC Microbiology Department will be responsible for performing processing of routine environmental monitoring samples, product-release testing, and raw material ...

Quality Control Analyst

Holly Springs, NC · On-site

$20.75 - $28/hr

Quality Control Analyst Location: Holly Springs, Wake County, North Carolina Job Type: Contract Duration: 12 months * Responsibilities: * Perform raw material compendia chemistry testing for QC ...

Quality Control Analyst

Covington, GA · On-site

$20.25 - $27.25/hr

The Quality Control Analyst is responsible for performing quality assurance and quality control activities across assigned projects to ensure mechanical systems and installations meet design ...

Showing results 21-40

Biotechnology Quality Control Analyst information

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$16

$27

$41

How much do biotechnology quality control analyst jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for biotechnology quality control analyst in the United States is $27.92, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $31.01 per hour, depending on experience, location, and employer.

What is the difference between Biotechnology Quality Control Analyst vs Microbiologist?

AspectBiotechnology Quality Control AnalystMicrobiologist
Required CredentialsBachelor's in biology, microbiology, or related field; GMP and GLP training often preferredBachelor's or higher in microbiology, biology, or related field; specialized microbiology certifications
Work EnvironmentLaboratories focused on product testing, quality assurance, and compliance in biotech/pharmaceutical industriesResearch labs, healthcare settings, or environmental testing labs, often involving microbial analysis
Employer & Industry UsageBiotech, pharmaceutical, and biotech manufacturing companiesResearch institutions, healthcare, environmental agencies, and biotech firms

The Biotechnology Quality Control Analyst primarily focuses on testing and ensuring the quality of biotech products, adhering to regulatory standards. In contrast, a Microbiologist often conducts research or analyzes microbial samples across various settings. While both roles require microbiology knowledge and lab skills, the QC analyst emphasizes compliance and product safety, whereas microbiologists may engage in broader scientific research.

What cities are hiring for Biotechnology Quality Control Analyst jobs?

Cities with the most Biotechnology Quality Control Analyst job openings:

What are popular job titles related to Biotechnology Quality Control Analyst jobs?

For Biotechnology Quality Control Analyst jobs, the most frequently searched job titles are:

Infographic showing various Biotechnology Quality Control Analyst job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $58,065 per year, or $27.9 per hour.

$24.50 - $33/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago


Job description

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases. From our global network of research and development sites, we are committed to discovering and developing safe, effective, and cutting-edge therapies for patients worldwide.Legend Biotech entered into a global collaboration agreement with Johnson & Johnson to jointly develop and commercialize CARVYKTI® (ciltacabtagene autoleucel; cilta-cel). Through this strategic partnership, we combine complementary expertise and capabilities to advance innovative immunotherapies for patients living with multiple myeloma.Legend Biotech is seeking a QC Analyst as part of the Quality Operations team based in Raritan, NJ.Role OverviewThe 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 ResponsibilitiesBe 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.RequirementsBachelor'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-BZ1#Li-OnsiteThe 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): $68,045—$89,308 USDPlease note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.Work Authorization & Employment EligibilityApplicants must be authorized to work in the United States. As part of our commitment to maintaining a lawful workforce and ensuring compliance with federal employment regulations, we participate in the E-Verify program. If you are selected for employment, you will be required to complete the Form I-9 process, and your employment eligibility will be verified through E-Verify in accordance with applicable federal law. We are committed to providing a fair, transparent, and welcoming hiring experience for all candidates.EEO StatementIt 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. Salary: . Date posted: 09/03/2026