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Quality Control Associate

Location: Somerville, NJ, United States
Job Type: Full Time
Job Category: Pharmaceutical and Biotech
Job Industry: Pharmaceuticals and Medical Products
Salary: We offer competitive compensation and benefits.
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The Opportunity


We're looking for Quality Control Associate, working in Pharmaceuticals and Medical Products industry in Somerville, New Jersey, 08876, United States.

  • Performs inspections following procedures, specifications and applicable standards and regulations.
  • Provides technical support to cross-functional teams as needed, identifies potential discrepancies and non-conformance and alert management.
  • Performs porcine and human tissue receipt, and inspection, in-process inspections i.e. ebeam), and performs product discard as per procedures in an electronic data system.
  • Supports and partners with cross-functional teams to resolve any issues or non-conformance encountered.
  • Performs applicable actions for Non-conformance Reports (NCRs), Supplier Issues (SIs), Engineering Change Orders (ECOs), etc.

Our Client

Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.

Experience Required for Your Success

  • Associate's or Bachelor’s degree preferred.
  • 1 to 2 years of experience in a GMP environment performing Quality Inspection
  • Ability to carry and lift boxes weighing up to 50 lbs.
  • Ability to work varied schedule with some potential weekend, early morning or late evening hours, if needed.
  • Majority of work performed in a warehouse or manufacturing setting.
  • Must be willing to work with potentially biohazardous materials, including cadaveric tissue.
  • Ability to walk, lift, bend, climb, squat, stoop, stretch, stand, and sit for long periods of time.
  • Must be willing to work with potentially biohazardous materials.
  • AATB certification preferred.
  • Advanced computer skills - high knowledge and understanding of Windows based computer systems such as Microsoft Office Suite.
  • Experience with Current Good Manufacturing Practices (cGMPs) and working in a regulated industry;
  • Familiarity with AATB, ISO, FDA, and/or USP regulations guidelines.
  • Experience with Enterprise Resource Planning (ERP) software, such as Oracle or SAP.
  • Demonstrated knowledge of Quality Control inspection techniques.
  • Basic knowledge of statistical techniques and quality tools.
  • Strong organizational abilities and problem-solving skills.

What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply Now

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