Upstream Biotech Manufacturing Specialist — Single-Use Systems

JMD Technologies Inc.; Milford (MA); On-site; USD 48,000 - 59,000; Full time

Job summary

JMD Technologies Inc. in Massachusetts seeks an Upstream Manufacturing Associate III to support upstream/cell culture and single-use manufacturing in a cGMP cleanroom.

The role follows an overnight 6:00 PM–6:30 AM schedule, including weekends as required. You will perform upstream/biologics operations, aseptic processing, BSC work, and sampling, while documenting batch parameters and production records per GDP/GMP.

Qualifications

• 5+ years of upstream manufacturing experience in biopharma.
• Single-use manufacturing experience is required.
• Knowledge of cGMP, aseptic techniques and cleanroom operations.
• Experience with cell culture, process equipment, tanks, autoclaves, or chromatography equipment.
• High school diploma with 7+ years related experience, or Associate/Bachelor's degree in Life Sciences/Engineering.

Responsibilities

• Perform upstream and biologics manufacturing operations using process equipment and single-use systems.
• Perform aseptic processing, BSC operations, and sampling per cGMP requirements.
• Monitor and document batch parameters, computer data, and production records according to GDP/GMP standards.
• Troubleshoot process issues, respond to alarms, and document unplanned events.
• Support training, continuous improvement, and cross-functional manufacturing discussions.
• Maintain production areas and handle manufacturing supplies and equipment as required.

Skills

GMP documentation

Upstream manufacturing

Aseptic/cleanroom

Batch documentation

Process equipment knowledge

Education

High school diploma with 7+ years related experience

Associate/Bachelor's degree in Life Sciences/Engineering

Tools

Microsoft Word

Microsoft Excel

Job description

JMD Technologies Inc. in Massachusetts seeks an Upstream Manufacturing Associate III to support upstream/cell culture and single-use manufacturing in a cGMP cleanroom.

The role follows an overnight 6:00 PM–6:30 AM schedule, including weekends as required. You will perform upstream/biologics operations, aseptic processing, BSC work, and sampling, while documenting batch parameters and production records per GDP/GMP.