The Opportunity

We're looking for a Quality Control Analyst, working in the Pharmaceuticals & Medical Products industry in Swiftwater, Pennsylvania, United States.

  • Provides QC facilities support and provides material receipt/distribution, waste removal, product inventorying, and GMP documentation preparation/certification.
  • Performs cycle count/inventory, orders, receives, stocks, and distributes materials for use in/by QC laboratories on a timely basis to ensure laboratory operations are able to continuously operate.
  • Handles and discards laboratory waste, including boxing up in biohazard boxes/buckets, autoclaving and delivering the waste to the dock for disposal and initiating transportation requests.
  • Monitors inventory of product in a GMP environment, including making adjustments in various systems (LIMS/SAP) as needed.
  • Performs Preparation/Certification of laboratory logbooks and follows proper GMP and HSE practices for handling of materials, including company products and biohazard, and will also be required to document activities such as autoclave operation, in accordance with good documentation practices.
Details

The pay range we are offering is 10 to 13 per hour. This position may present an opportunity to go permanent.

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
  • HS diploma
  • 1-3 years of experience in a GMP environment with knowledge of biosafety practices preferred
  • Ability to follow proper GMP and HSE practices for handling of materials, including company products and biohazard material
  • Ability to document activities such as autoclave operation, in accordance with good documentation practices
  • Ability to handle/lift up to 50 lbs. required 
  • Ability to use dock and material handling equipment, such as pallet jacks, to transport larger quantities of materials is also required
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 here.

Not exactly? Join Our Talent Community, and we'll let you know of additional opportunities.

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