Quality Control Associate Role at Bio-Techne USA
Bio-Techne is hiring a Quality Control Associate in Newark, California, for a full-time role supporting product release testing in life sciences and clinical diagnostics. This quality control job is ideal for candidates with hands-on laboratory experience who want to work in a GMP and ISO 13485 regulated environment. Join Bio Techne and contribute to high-impact research that helps treat and prevent diseases worldwide.
Job Details:
- Job Title: Quality Control Associate
- Location: Newark, California, USA
- Employment Type: Full Time
- Job Requisition ID: JR101444
- Industry: Life Sciences & Clinical Diagnostics
- Pay Range: $46,100.00 – $75,800.00 per year
- Work Environment: Quality Control laboratory and office setting
About the Company:
Bio-Techne is a global life sciences company dedicated to enabling cutting-edge research in life sciences and clinical diagnostics. Through its diverse portfolio of brands, Bio Techne provides high-quality tools and solutions that help researchers advance science, treat diseases, and improve patient outcomes worldwide. Explore more quality control job offers in USA.
Educational Requirements:
- B.S./B.A. in Molecular Biology, Biochemistry, Cell Biology, or a related field with 1+ years of relevant laboratory experience
OR - Associate’s degree in Molecular Biology, Biochemistry, Cell Biology, or a related field with 2+ years of relevant laboratory experience
Key Responsibilities for Quality Control Associate Role:
- Perform analytical and functional testing for in-process and finished goods
- Conduct analytical and functional testing on incoming raw materials
- Carry out stability product testing to extend product dating
- Perform slide imaging and scanning for functional assays
- Review QC data and assess results against acceptance criteria
- Record, track, and maintain quality control data in logs and spreadsheets
- Prepare QC reference standards, control stocks, and cultures
- Initiate nonconformance and deviation reports
Skills Required for Quality Control Associate Role:
- Experience in molecular biology techniques, microscopy, and imaging
- Strong attention to detail with excellent organizational skills
- Ability to work independently and as part of a team
- Excellent written and verbal communication skills
- Experience in a Quality Control environment preferred
- Familiarity with Leica BOND III, BOND Rx, or Roche Ventana Ultra is a plus
- Experience with slide imaging scanners is an advantage
- Knowledge of ISO 13485 and GMP environments is a plus
Benefits of the Quality Control Associate Role:
- Competitive medical, dental, and vision insurance from day one
- Life, short-term disability, long-term disability, pet, legal, and ID protection plans
- 401(k), Employee Stock Purchase Plan (ESPP), HSA, FSA, and Dependent Care FSA
- Career development through mentorship, training, tuition reimbursement, and promotions
- Paid holidays, paid time off, and paid parental leave
- Employee resource groups, volunteer PTO, and community events
- Inclusive and innovative workplace culture
