Manufacturing Associate

SGS Consulting
Massachusetts

Job Responsibilities:

  • Manage own time and professional development, be accountable for own results and begin to prioritize own workflow.
  • Cross-functional communication with tech transfer team, quality and engineering as necessary.
  • Implement {Current} Good Manufacturing Practices {part of GxP} procedures and safe handling techniques for solid dosage processing within the continuous manufacture /PCMM work stream.
  • Ability to follow Standard Operating Procedures and work under minimal supervision.
  • Identify and support continuous improvement initiatives and root cause analysis tools.
  • Generate, assist and execute documentation associated with solid dosage manufacture, such as, working batch record documentation, in-process run sheets.
  • Complete activities identified as Operator care tasks associated with the maintenance and operation of complex pharmaceutical manufacturing equipment.
  • Actively participate in shift exchange activities and communication channels.
  • Complete training to take part in safety inspections within the facility.
  • Manage solution preparation and laboratory consumables.
  • Understand and comply with the policies, procedures and working practices of Environment, Health & Safety and where necessary contribute to the review and implementation of the practices in the plant.
  • Help to coordinate shipments of solutions and medias to other sites.

Skills:

  • Demonstrated experience in a biotechnology manufacturing or laboratory environment
  • Operational knowledge of computerized systems, Familiarity with Production Control Systems, Enterprise Resource Planning Systems and other business systems
  • Maintains a safe work environment
  • Demonstrated capability to work as a team member in a matrix development team
  • Excellent oral and written communication skills
  • Strong computer skills in Microsoft Office required, especially MS Word, MS Excel

Education/Experience:

  • High School
Posted 2026-04-22

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