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Manufacturing Associate

Job in Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: JMD Technologies Inc.
Full Time position
Listed on 2026-10-13
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Validation Engineer
Salary/Wage Range or Industry Benchmark: 40 - 55 USD Hourly USD 40.00 55.00 HOUR
Job Description & How to Apply Below

Title:
Sr. Manufacturing Associate & Manufacturing Specialist

Employment Type:
Contract

Status:
Accepting Candidates

About the Role

We are seeking a Manufacturing Specialist to support clinical cell therapy manufacturing in a cGMP environment. This role serves as a floor SME and focuses on hands-on aseptic processing, batch record and procedure authoring/review, right-first-time execution, technical projects, technology transfer, and accelerated onboarding.

Key Responsibilities Cell Therapy Manufacturing
  • Perform clinical product manufacturing for cell therapy according to cGMP standards
  • Assemble raw materials, follow SOPs, perform aseptic processing, complete batch records, and report deviations
  • Demonstrate and assist others with aseptic technique
  • Ensure cGMP compliance through consistent execution
  • Serve as the floor SME for manufacturing activities
  • Author and review batch records and procedures
  • Support same-day documentation activities
  • Support development of SOPs and other manufacturing documentation in collaboration with Development and Quality groups
Technical Projects & Operations
  • Support technology transfer and final process development from Development to Manufacturing
  • Support technical projects and manufacturing initiatives
  • Ensure raw materials are identified and available in time for manufacturing activities
  • Transfer raw materials inside cleanroom suites using sanitizing reagents
  • Support coordination of resources within the Operations group
  • Work in a cleanroom and office setting
  • Occasionally move lab equipment and materials weighing up to 50 pounds
  • Work with compressed gases and LN2
Qualifications
  • 5–6 years of cGMP cell therapy manufacturing experience
  • Hands-on aseptic technique/aseptic processing experience
  • Experience authoring and reviewing batch records and procedures
  • Strong cGMP manufacturing experience
Preferred Qualifications
  • Leadership experience is a strong plus
  • Experience serving as a manufacturing floor SME
  • Experience supporting technical projects and technology transfer
  • Experience driving right-first-time execution
  • Ability to complete an accelerated onboarding
Compensation
  • $40–$55/hr
  • Tuesday–Saturday, 9:00 PM–7:30 AM
  • 40 hours/week
  • 6+ Month Contract with possibility of extension or conversion
Position Requirements
10+ Years work experience
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