Biopharma GMP Manufacturing Technician

Actalent; Plainville (CT); On-site; USD 43,000 - 48,000; Part time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance (Voluntary Life & AD&D)

Short and long-term disability

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

Time Off/Leave (PTO, Vacation or Sick)

Job summary

Actalent in Plainville, MA, is seeking a contract manufacturing professional with technical expertise in biopharmaceutical manufacturing equipment and GMP compliance. You will navigate a dynamic environment, balance priorities, and learn new software tools while reporting to operators or management.

This role requires at least 1 year of manufacturing-related experience; cGMP exposure is preferred. The position is fully onsite in Plainville, with benefits including medical, dental, vision,

Qualifications

• Minimum of 1 year of work experience in manufacturing, operations, production, lab setting or related field.
• Preferred: Experience in a cGMP environment.

Responsibilities

• Apply technical expertise in biopharmaceutical manufacturing equipment and processes with attention to GMP standards.
• Make decisions for moderately complex GMP manufacturing activities with minimal to moderate supervision and communicate with operators or management.
• Maintain accurate operational documents to support GMP compliance and traceability.

Skills

1 year manufacturing experience

Job description

Actalent in Plainville, MA, is seeking a contract manufacturing professional with technical expertise in biopharmaceutical manufacturing equipment and GMP compliance. You will navigate a dynamic environment, balance priorities, and learn new software tools while reporting to operators or management.

This role requires at least 1 year of manufacturing-related experience; cGMP exposure is preferred. The position is fully onsite in Plainville, with benefits including medical, dental, vision,