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The Opportunity

We're looking for a Manufacturing/Laboratory Associate, working in the Pharmaceuticals & Medical Products industry in Minneapolis, Minnesota, United States.

  • Performs and documents daily manufacturing operations according to SOPs in a cGMP environment.
  • Operates biologics production equipment (bioreactors, filtration units, chromatography systems and fixed/portable vessels).
  • Performs basic troubleshooting and assists with processing steps and/or manufacturing activities by monitoring process parameters in batch record and control systems.
  • Documents cGMP data and information for processing steps and/or equipment activities while following standard operating procedures which includes batch records, work orders, and equipment logbooks.
  • Executes batch records and validation protocols under supervision/direction of others and would perform inventory transaction and data entry into SAP and LIMS.

We are offering Competitive Compensation and Benefits. 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
  • Bachelor's degree in Science or Engineering; or Associate's degree in Science-related area with 1+ year of relevant experience; or High school diploma/GED with 3+ years of relevant experience
  • Experience in a regulated environment preferred
  • Understanding of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) preferred
  • Familiar or experience with cGMP within Biotech or Pharmaceutical operations preferred
  • Knowledge of non-manufacturing functions such as QC, Regulatory, QA, and/or Materials Management preferred
  • Prior experience with lab equipment preferred
  • Ability to perform basic computer operations, such as the ability to navigate in MS Office, use email, and complete training using Web-Based Training (WBT)
  • Ability to work assigned shift (day or night)
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.