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Manufacturing Specialist – Cell Therapy
Job in
Boston, Suffolk County, Massachusetts, 02298, USA
Listed on 2026-09-25
Listing for:
JMD Technologies Inc.
Full Time
position Listed on 2026-09-25
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing & Industrial Operations, Production Associate / Production Line, Validation Engineer
Job Description & How to Apply Below
Job Title: Manufacturing Specialist – Cell Therapy
Employment Type: Contract
Hours: 40 Hours/Week | 9:00 PM – 7:30 AM
Status: Accepting Candidates – Multiple Openings
About the RoleWe are seeking a Manufacturing Specialist – Cell Therapy to support the production of clinical cell therapy products within a controlled cGMP manufacturing environment. This role will focus on aseptic processing, cleanroom operations, raw material preparation, and accurate manufacturing documentation.
Key Responsibilities- Support manufacturing activities for clinical cell therapy products.
- Perform aseptic processing activities in a controlled cleanroom environment.
- Prepare, transfer, and stage raw materials and manufacturing components.
- Execute and maintain accurate batch records and manufacturing documentation.
- Follow approved SOPs, GMP procedures, and safety requirements.
- Demonstrate proper aseptic technique and cleanroom practices.
- Identify and report deviations or manufacturing issues in a timely manner.
- Support technology transfer and process development activities as needed.
- Collaborate with Manufacturing, Quality, and Process Development teams.
- Maintain a clean, organized, and compliant manufacturing workspace.
- 2–4 years of hands-on manufacturing experience
, ideally in biotech, biopharma, or cell therapy settings. - Practical experience performing aseptic manufacturing or aseptic techniques
. - Working knowledge of cGMP practices and regulated manufacturing environments
. - Experience operating within cleanroom environments
, including proper gowning and material handling. - Ability to accurately complete batch records, SOPs, and other GMP-related documentation
. - Strong focus on accuracy, compliance, and following established manufacturing procedures.
- Capable of safely lifting and moving materials weighing up to 50 lbs.
- Effective communication skills with the ability to work collaboratively within cross-functional teams.
- Comfortable working a night/overnight shift and following the assigned schedule.
- Estimated hourly range: $50–$55/hr (W-2).
- Final rate within this range will be based on skills, experience, and interview results.
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