Manufacturing Operations Senior Associate (Contract) 77777

Atrium WorksBoston, MA
1d$38 - $42

About The Position

We are seeking a detail-oriented Manufacturing Operations Senior Associate with experience in aseptic processing and cleanroom operations. The ideal candidate will have hands-on experience working in Grade B cleanroom environments, executing batch processes, and maintaining accurate documentation in compliance with regulated laboratory and manufacturing standards. Current Shift: Wednesday - Saturday 7:00am - 2:30pm (This maybe updated to Tuesday-Saturday)

Requirements

  • HSD +3 years experience
  • Experience working in a laboratory or biopharmaceutical manufacturing environment
  • Hands-on experience with aseptic techniques and cleanroom operations (Grade B preferred)
  • Familiarity with batch record execution and GMP documentation practices
  • Experience with LIMS and MES systems
  • Proficiency in operating laboratory/manufacturing equipment such as peristaltic pumps, tube welders, and centrifuges
  • Strong attention to detail and ability to follow precise instructions
  • Good organizational and documentation skills

Nice To Haves

  • Experience in cell culture processing or bioprocessing
  • Prior experience in regulated environments such as pharmaceutical or biotech manufacturing

Responsibilities

  • Execute batch processing activities in a laboratory or manufacturing setting following established batch records and SOPs
  • Following Batch Records, SOPs, policies and all other relevant work instructions to ensure the successful and compliant operation of the drug product facility
  • Perform aseptic techniques and aseptic processing in a Grade B cleanroom environment
  • Prepare, process, and transfer media for cell culture operations, including filling, harvesting, filtering, and centrifugation
  • Handle downstream processes such as waste removal and transfer of final product into drug product bags
  • Operate and maintain equipment including peristaltic pumps, tube welders, and balances
  • Accurately document all laboratory and manufacturing activities in compliance with GMP standards
  • Utilize LIMS (Laboratory Information Management Systems) and MES (Manufacturing Execution Systems) for data entry, tracking, and reporting
  • Ensure adherence to safety, quality, and regulatory requirements at all times
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