Cell Therapy Manufacturing Specialist (Aseptic, cGMP)

JMD Technologies Inc.; Boston (MA); On-site; USD 55,000 - 76,000; Full time

Job summary

JMD Technologies Inc. is seeking a Sr. Manufacturing Associate & Manufacturing Specialist to support clinical cell therapy manufacturing in a cGMP environment.

This role serves as a floor SME, focusing on hands-on aseptic processing, batch record and procedure authoring and review, and right-first-time execution. Key responsibilities include assembling materials, following SOPs, reporting deviations, and supporting technology transfer and documentation with Development and Quality teams.

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.

Responsibilities

• 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

Skills

cGMP manufacturing

Aseptic technique

Batch record writing

Cross-functional collaboration

Job description

JMD Technologies Inc. is seeking a Sr. Manufacturing Associate & Manufacturing Specialist to support clinical cell therapy manufacturing in a cGMP environment.

This role serves as a floor SME, focusing on hands-on aseptic processing, batch record and procedure authoring and review, and right-first-time execution. Key responsibilities include assembling materials, following SOPs, reporting deviations, and supporting technology transfer and documentation with Development and Quality teams.