(TEMP) Manufacturing Associate V

Job Locations US-GA-Union City
Job ID


The Temporary Manufacturing Associate V is responsible for aseptic manufacturing and assembly of clinical and commercial human blood derived components in a clean-room environment (Class 10,000/ISO7, and Class 100,000/ISO8).



  • Weighs, measures and checks raw materials to ensure batches manufactured contain proper ingredients and quantities.
  • Maintains records to comply with regulatory requirements and acts as subject matter expert for revisions or improvements to manufacturing documents.
  • Works with other Cell Processing Associates utilizing good manufacturing practices during aseptic processing of clinical and commercial products using Standard Operating Procedures.
  • Represents department in cross-functional teams, projects and GXP-related problem resolution.
  • Posts weights and shipping charges, and prepares goods for final shipment.
  • Prepares and maintains records of merchandise shipped.
  • Prepares goods for final shipment and unpacks and checks goods received against purchase orders and invoices, maintains records of received goods, rejecting unsatisfactory items if necessary.
  • Examines, stocks, and distributes GMP and non-GMP materials to inventory and manufacturing lines.
  • Other duties as assigned
  • Applies job skills and company policies and procedures to complete a wide range of tasks.
  • Works on assignments that are moderately complex in nature where judgment is required in resolving problems and making routine recommendations.
  • Normally receives general instructions on routine work, detailed instructions on new assignments.
  • Uses ability as a skilled specialist in accordance with company policies and procedures to compete complex tasks in creative and effective ways.
  • Works on assignments that are complex in nature where considerable judgment and initiative are required in resolving problems and making routine recommendations.
  • May determine methods and procedures on new assignments and may provide guidance to other support personnel.




  • Associate’s or Medical Technical degree or equivalent.
  • Typically 2 years related experience in CGMP/FDA regulated industry or 1 year with Medical Technical degree.
  • Proficient in MS Office applications.


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