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Quality Control Biology Jobs (NOW HIRING)

Union Agener

QC Biologist II

Augusta, GA · On-site

... of the QC Manager. • Assists in coordinating FDA inspections and responses to FDA-483 ... S. Degree in Microbiology or other Biological Science required. Experience: • Familiar with ...

Frontage Laboratories

QC Manager

Exton, PA · On-site

Biomarker & Biologics Location: Exton, PA ( Onsite) Position Summary The QC Manager is responsible for oversight of the Quality Control function supporting compliant biologics and biomarker testing ...

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How much do quality control biology jobs pay per hour?

As of Jul 9, 2026, the average hourly pay for quality control biology in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

What do QC scientists do?

Quality Control (QC) scientists in biology are responsible for testing and analyzing biological samples to ensure products meet quality standards and regulatory requirements. They perform experiments, use laboratory instruments, and document results to identify any deviations or contamination. Their work supports product safety, efficacy, and compliance in industries like pharmaceuticals, biotech, and food production.

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

To thrive as a Quality Control Biology professional, you need a strong background in biological sciences, laboratory techniques, and data analysis, typically supported by a relevant degree in biology or a related field. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and analytical instruments like HPLC and PCR is essential. Attention to detail, problem-solving abilities, and effective communication are standout soft skills in this role. These competencies ensure accurate testing, regulatory compliance, and the delivery of safe, high-quality biological products.

What does a QC specialist do in biotech?

A QC (Quality Control) specialist in biotech is responsible for testing and inspecting biological products to ensure they meet quality standards and regulatory requirements. They perform assays, analyze data, and document results using laboratory instruments and techniques, often working with GMP (Good Manufacturing Practice) protocols. Their role helps ensure product safety, efficacy, and compliance throughout the manufacturing process.

What is Quality Control Biology?

Quality Control Biology refers to the process of ensuring that biological products, such as pharmaceuticals, vaccines, or laboratory reagents, meet established standards for safety, efficacy, and quality. Professionals in this field perform tests on biological samples to detect contaminants, verify potency, and confirm that products comply with regulatory requirements. Their work is critical in the manufacturing process to prevent the release of faulty or unsafe products. Quality Control Biologists use a variety of analytical techniques and must maintain detailed records to support compliance with industry regulations.

How to become a biotech quality control specialist?

To become a biotech quality control specialist, candidates typically need a bachelor's degree in biology, microbiology, biochemistry, or a related field. Relevant skills include knowledge of laboratory techniques, quality assurance protocols, and familiarity with regulatory standards such as GMP or ISO. Certifications like ASQ Quality Auditor can enhance job prospects, and experience with laboratory instruments and data analysis is often required.

What are some common challenges faced by professionals in Quality Control Biology, and how can they be managed?

Professionals in Quality Control Biology often face challenges such as tight deadlines for sample analysis, managing multiple testing priorities, and ensuring strict compliance with regulatory standards. Effective time management and strong organizational skills are essential to handle overlapping projects and urgent requests. Additionally, clear communication and collaboration with other departments, such as production and quality assurance, can help resolve discrepancies quickly and maintain high testing accuracy. Ongoing training and staying updated on evolving industry regulations also contribute to managing these challenges successfully.

What is the difference between Quality Control Biology vs Quality Assurance Biology?

AspectQuality Control BiologyQuality Assurance Biology
CertificationsTypically requires a Bachelor's degree in Biology or related fieldRequires similar degrees; certifications like ASQ may be beneficial
Work EnvironmentLaboratories, manufacturing plants, testing facilitiesQuality management departments, compliance offices
Industry UsageUsed in biotech, pharmaceutical, food industries for testing productsUsed in developing and maintaining quality systems and standards
Search & Comparison IntentFocuses on testing and product quality checksFocuses on system processes and compliance standards

While both roles involve ensuring product quality, Quality Control Biology primarily focuses on testing and inspecting biological products, whereas Quality Assurance Biology emphasizes developing and maintaining quality systems and standards within the industry.

What biology jobs pay over $100k?

In the field of biology, roles such as senior research scientist, biotech director, or regulatory affairs manager often have salaries exceeding $100,000 annually. These positions typically require advanced degrees, specialized skills, and experience in areas like molecular biology, biochemistry, or laboratory management.
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Quality Control Biology jobs near you
Infographic showing various Quality Control Biology job openings in the United States as of July 2026, with employment types broken down into 76% Full Time, 21% Part Time, 1% Temporary, and 2% Contract. Highlights an 81% Physical, 1% Hybrid, and 18% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.
Supervisor, Quality Control Biology

Supervisor, Quality Control Biology

Artiva Biotherapeutics, Inc.

San Diego, CA

$135K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago

Job description

About Artiva:

We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate,AlloNK, is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.


For more information, visit
www.artivabio.com.


Job Summary:

Artiva Biotherapeutics is seeking a skilled and motivated Quality Control Supervisor who will be reporting to the Senior Manager, Quality Control. This individual will supervise the Bio Team and support QC biology testing. The individual will additionally perform routine cGMP release and stability testing of Artiva's products.

Duties/Responsibilities:

  • Write and revise SOPs/Test methods that support Artiva's cell therapy products.
  • Operate and test ELISA, Flow Cytometers, automated cell counters, and other analytical instruments and equipment, as needed.
  • Serve as primary QC Biology point of contact for cross-functional teams including Manufacturing, QA, and Regulatory Affairs for release and investigation activities.
  • Lead training and qualification of Bio team members on equipment use and biological test methods.
  • Support activities for QC equipment IQ/OQ/PQs.
  • Lead and perform routine cGMP release and stability testing of Artiva's products; including biological tests, biochemistry, chemistry-based tests as needed.
  • Lead evaluation of QC systems and/or implementation of system improvements.
  • Perform laboratory investigations and write reports for deviations.
  • Ensure data integrity practices (ALCOA+ principles) are followed by the Bio team; support LIMS/ELN implementation and administration as applicable.
  • Assist in laboratory investigations for Out of Specification results.
  • Assist in biological method qualification and validation as needed.
  • Perform periodic trending of QC testing data; identify adverse trends and initiate CAPAs as appropriate.
  • Perform all work according to company policies, SOPs, and cGMP practices.
  • Planning and scheduling for GMP in-process and release testing.
  • Reviewing biology data and investigating OOS and OOT results.
  • Write technical QC protocols and reports as needed.
  • Assist QC and AD team for analytical qualification and validation, as necessary.
  • Develop an in-depth understanding of NK and CAR-NK products, testing, and safety.
  • Maintain records and databases in accordance with procedures.

Qualifications:

  • Bachelor's degree (BS/BA) in Biology, Biochemistry, Immunology, or a related life science field required.
  • Experience with NK cell or CAR-modified cell therapy products preferred; familiarity with viability, cytotoxicity, identity, and potency assays for cell therapy products.
  • Minimum 8 years of cGMP QC experience in a cell therapy/biotech/pharmaceutical setting is required.
  • At least 1 year of Supervisory or team lead experience is required.
  • Knowledge and experience in supporting cGMP deviations, OOS, etc.
  • Basic knowledge of method transfers, qualifications, and validations; current industry practices; and strong experience with guidance interpretation and application
  • Excellent critical thinking and technical writing skills.
  • Computer skills required to operate Microsoft Word, Project, Visio, and Excel programs.


In addition to a great culture, we offer:

  • A beautiful facility
  • An entrepreneurial, highly collaborative, and innovative environment
  • Comprehensive benefits, including:
  • Medical, Dental, and Vision
  • Group Life Insurance
  • Long Term Disability (LTD)
  • 401(k) Retirement Plan
  • Employee Assistance Program (EAP)
  • Flexible Spending Account (FSA)
  • Paid Time Off (PTO)
  • Company paid holidays, including the year-end holiday week
  • Our recognition program, Bonus.ly, is where you can trade in points earned for things you want.

If all this speaks to you, come join us on our journey!

Base Salary: $ 110,000 - $135,000. Exact compensation may vary based on level, skills and experience.

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