Biopharma GMP Manufacturing Technician – Night Shift

Kelly Services; Plainville (MA); On-site; USD 25,000 - 36,000; Part time

Job summary

Kelly Services is seeking a Manufacturing Associate for a premier client in Plainville, MA 02762. The role emphasizes executing work instructions, maintaining batch records, and ensuring GMP compliance.

Daily duties include inspecting products, assisting with batch reconciliation, and adhering to quality systems. You will spend about 90% of time in manufacturing suites, support training, and follow GDP and cleanroom gowning protocols.

Qualifications

• High school diploma or equivalent required.
• Minimum 1 year experience in manufacturing, operations, production, lab setting or related field.
• Experience in a cGMP environment preferred.
• PPE provided; no steel toes, but closed-toed shoes; GMP regulations followed.
• Ability to read/write GMP documentation and follow GDP/cleanroom gowning.
• Able to aseptically gown as needed and maintain safety practices.
• Regularly spend time in manufacturing suites and maintain batch records.
• Strong attention to quality, safety and regulatory requirements.

Responsibilities

• Execute work instructions and complete assignments.
• Maintain inventory records and batch records.
• Inspect finished products for adherence to specifications.
• Assist with batch record reconciliation and preventative maintenance.
• Adhere to Quality Management Systems and CAPA closures.
• Identify and escalate items requiring attention.
• Maintain a clean and safe work environment.
• Follow safety, GDP, and cleanroom gowning policies.
• Spend 90% of time in manufacturing suites.

Skills

Biopharma equipment

GMP knowledge

Dynamic environment

Learning software/tools

Decision making

Written/verbal communication

Aseptic gowning

Documentation review

Safety compliance

Gowning GMP regs

Education

High school diploma or equivalent

Job description

Kelly Services is seeking a Manufacturing Associate for a premier client in Plainville, MA 02762. The role emphasizes executing work instructions, maintaining batch records, and ensuring GMP compliance.

Daily duties include inspecting products, assisting with batch reconciliation, and adhering to quality systems. You will spend about 90% of time in manufacturing suites, support training, and follow GDP and cleanroom gowning protocols.