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Manufacturing Associate

Job in Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: Meet Life Sciences Ltd.
Full Time position
Listed on 2026-10-10
Job specializations:
  • Manufacturing / Production
    Manufacturing & Industrial Operations, Pharmaceutical Manufacturing, Lean Manufacturing / Six Sigma, Production Manager
Salary/Wage Range or Industry Benchmark: 65000 - 90000 USD Yearly USD 65000.00 90000.00 YEAR
Job Description & How to Apply Below

The Manufacturing Associate is responsible for supporting GMP manufacturing operations with a focus on cell culture processes, operational excellence, and compliance. This role requires a hands-on manufacturing professional who can work independently on third shift, support quality-related activities, and provide on-the-job training to manufacturing staff. The ideal candidate has extensive manufacturing experience, strong problem-solving skills, and the ability to ensure safe, efficient, and compliant production operations.

Responsibilities
  • Perform manufacturing operations in accordance with GMP requirements, standard operating procedures (SOPs), and batch records.
  • Execute cell culture processes and support routine manufacturing activities to ensure production goals are achieved.
  • Work independently with minimal supervision while maintaining high standards of quality and compliance.
  • Investigate and document manufacturing deviations and support Quality Management System (QMS) activities, including CAPA-related processes.
  • Identify, troubleshoot, and resolve manufacturing issues to minimize downtime and maintain operational efficiency.
  • Conduct on-the-job training for manufacturing personnel and ensure adherence to established procedures and best practices.
  • Maintain accurate manufacturing documentation and ensure timely completion of production records.
  • Collaborate with cross-functional teams, including Quality, Manufacturing, and Technical Operations, to support continuous improvement initiatives.
  • Promote a safe working environment and ensure compliance with GMP, safety, and company policies.
Qualifications
  • Minimum of 3 years of experience in manufacturing or manufacturing-adjacent roles within a regulated environment.
  • Broad hands-on experience with cell culture manufacturing processes is strongly preferred.
  • Experience with deviation investigations and Quality Management Systems (QMS), including CAPA processes, is highly preferred.
  • Demonstrated ability to work independently with minimal oversight, particularly in an off-shift or third-shift manufacturing environment.
  • Experience training and mentoring manufacturing personnel through on-the-job instruction is highly desirable.
  • Strong understanding of GMP regulations, documentation practices, and manufacturing compliance requirements.
  • Excellent communication, organizational, and problem-solving skills with the ability to manage multiple priorities in a fast-paced manufacturing environment.
Position Requirements
10+ Years work experience
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