Senior Cell Therapy Manufacturing Associate – Aseptic Processing
JMD Technologies Inc. · Boston, MA
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Contract
Posted Sep 22, 2026
40–47 an hour
Job Description
Title: Senior Cell Therapy Manufacturing Associate – Aseptic Processing
Location: Greater Boston Area, MA (Onsite)
Employment Type: Contract
Hours: 40 Hours a week, 9pm - 7:30AM, Sunday-Wed or Wed-Saturday
Status: Accepting Candidates (Multiple opening)
About the role
Support the manufacturing of clinical cell therapy products in a cGMP environment. This hands-on role focuses on aseptic processing, cleanroom operations, raw material preparation, and accurate batch record execution.
Key Responsibilities
• Perform clinical cell therapy manufacturing activities according to cGMP standards.
• Execute aseptic processing, raw material preparation, SOPs, and batch records.
• Demonstrate and assist others with aseptic technique.
• Transfer and sanitize raw materials within the cleanroom suite.
• Report deviations and support technology transfer and process development activities.
• Support SOP and manufacturing documentation activities with Development and Quality teams.
Qualifications
• 2–4 years of manufacturing experience required.
• Hands-on aseptic technique / aseptic processing experience.
• Experience working in a regulated cGMP manufacturing environment.
• Experience with SOPs and batch record execution.
• Ability to work in a cleanroom and move about during processing activities.
• Ability to occasionally move equipment and materials weighing up to 50 pounds.
Compensation (MA Pay Transparency):
• Estimated hourly range: $40–$47/hr (W-2).
• Final rate within this range will be based on skills, experience, and interview results.
Location: Greater Boston Area, MA (Onsite)
Employment Type: Contract
Hours: 40 Hours a week, 9pm - 7:30AM, Sunday-Wed or Wed-Saturday
Status: Accepting Candidates (Multiple opening)
About the role
Support the manufacturing of clinical cell therapy products in a cGMP environment. This hands-on role focuses on aseptic processing, cleanroom operations, raw material preparation, and accurate batch record execution.
Key Responsibilities
• Perform clinical cell therapy manufacturing activities according to cGMP standards.
• Execute aseptic processing, raw material preparation, SOPs, and batch records.
• Demonstrate and assist others with aseptic technique.
• Transfer and sanitize raw materials within the cleanroom suite.
• Report deviations and support technology transfer and process development activities.
• Support SOP and manufacturing documentation activities with Development and Quality teams.
Qualifications
• 2–4 years of manufacturing experience required.
• Hands-on aseptic technique / aseptic processing experience.
• Experience working in a regulated cGMP manufacturing environment.
• Experience with SOPs and batch record execution.
• Ability to work in a cleanroom and move about during processing activities.
• Ability to occasionally move equipment and materials weighing up to 50 pounds.
Compensation (MA Pay Transparency):
• Estimated hourly range: $40–$47/hr (W-2).
• Final rate within this range will be based on skills, experience, and interview results.
Additional Details
- City
- Boston
- State
- Massachusetts
- Country
- US
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