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Assistant Biotech Quality Control Jobs (NOW HIRING)

Insight Global

Quality Control Assistant

Muskogee, OK · On-site

$50K - $60K/yr

Coordinate with field teams and QC personnel to collect project information * Assist with document distribution and version control * Support audits and quality compliance efforts * Generate reports ...

Legend Biotech US

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 Raritan, NJ . Role Overview The QC Analyst (IPL) is an exempt level position with responsibilities for ...

Top Guy Shoes

Quality Control Assistant

Walnut, CA · On-site

$20 - $24/hr

The Quality Control Assistant supports the Shipping and Purchasing team in ensuring that all footwear and apparel products meet Top Guy Shoes' standards for quality, safety, and compliance before ...

Top Guy Shoes

Quality Control Assistant

Walnut, CA · On-site

$20 - $24/hr

The Quality Control Assistant supports the Shipping and Purchasing team in ensuring that all footwear and apparel products meet Top Guy Shoes' standards for quality, safety, and compliance before ...

Precigen, Inc

QC Manager

Germantown, MD · On-site

$95K - $120K/yr

... and biotech industry under GMP guidelines, with demonstrated expertise in multiple disciplines and assays. * 2+ years of supervisory experience. * Advanced experience with QC testing in ...

Top Guy Shoes

Quality Control Assistant

Walnut, CA · On-site

The Quality Control Assistant supports the Shipping and Purchasing team in ensuring that all footwear and apparel products meet Top Guy Shoes' standards for quality, safety, and compliance before ...

Bruker

QC Inspector

Bothell, WA · On-site

$41K - $66K/yr

At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...

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Assistant Biotech Quality Control information

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How much do assistant biotech quality control jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for assistant biotech quality control in the United States is $22.84, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $23.08 per hour, depending on experience, location, and employer.

What is the difference between Assistant Biotech Quality Control vs Laboratory Technician?

AspectAssistant Biotech Quality ControlLaboratory Technician
CredentialsAssociate degree or equivalent, relevant certificationsAssociate degree or diploma, technical training
Work EnvironmentBiotech labs, quality assurance settingsResearch labs, clinical or industrial labs
Employer & IndustryBiotech companies, pharmaceutical firmsResearch institutions, healthcare, manufacturing
Common TasksSample testing, data recording, quality checksSample preparation, equipment operation, data collection

Assistant Biotech Quality Control and Laboratory Technicians both work in laboratory settings, often with overlapping skills. However, quality control roles focus more on ensuring product standards and compliance, while laboratory technicians may be involved in broader research or testing tasks. Understanding these differences helps job seekers target the right roles in the biotech industry.

More about Assistant Biotech Quality Control jobs
What cities are hiring for Assistant Biotech Quality Control jobs? Cities with the most Assistant 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 Assistant Biotech Quality Control jobs? States with the most job openings for Assistant Biotech Quality Control jobs include:
What job categories do people searching Assistant Biotech Quality Control jobs look for? The top searched job categories for Assistant Biotech Quality Control jobs are:
Assistant Biotech Quality Control jobs near you
Infographic showing various Assistant Biotech Quality Control 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 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $47,500 per year, or $22.8 per hour.

Supervisor, Quality Control Biology

Artiva Biotherapeutics, Inc.

San Diego, CA • On-site

$110K - $135K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 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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