Manufacturing Technician (cGMP) - Multiple Shifts

BioPharma Consulting JAD Group

Norton (MA)

On-site

USD 30,000 - 41,000

Full time

13 days ago

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Benefits offered by this job

Contract position with possible ext

Job summary

BioPharma Consulting JAD Group seeks Manufacturing Technicians with strong late‑stage manufacturing floor experience in a cGMP environment in Norton, MA. The role supports routine production activities across first, second, and third shifts.

You will operate, monitor, and clean production equipment, complete batch records, and assist in changeovers and in‑process checks while maintaining strict GDP documentation and safety guidelines.

Qualifications

  • Experience in a cGMP manufacturing environment.
  • Hands-on experience with late-stage floor operations.
  • Ability to work 1st, 2nd, or 3rd shift.
  • High attention to detail and adherence to regulated procedures.
  • High school diploma required; technical credentials preferred.

Responsibilities

  • Perform late-stage manufacturing operations following cGMP, SOPs, and safety guidelines.
  • Operate, monitor, and clean production equipment.
  • Complete batch records and GDP-compliant documentation.
  • Support material handling, line changeovers, and in-process checks.
  • Report deviations and assist in troubleshooting routine issues.
  • Collaborate with cross-functional teams to maintain production flow.
  • Follow environmental, health, and safety requirements at all times.

Skills

cGMP experience
Manufacturing floor ops
Shift flexibility
Attention to detail

Education

High School Diploma
Technical certificate or degree

Job description

We are seeking Manufacturing Technicians with strong late‑stage manufacturing floor experience in a cGMP environment. This role supports routine production activities across 1st, 2nd, and 3rd shift operations.

Responsibilities
  • Perform late‑stage manufacturing operations following cGMP, SOPs, and safety guidelines.
  • Operate, monitor, and clean production equipment.
  • Complete batch records and documentation according to GDP standards.
  • Support material handling, line changeovers, and in‑process checks.
  • Report deviations and assist in troubleshooting routine issues.
  • Collaborate with cross‑functional teams to maintain efficient production flow.
  • Follow environmental, health, and safety requirements at all times.
Qualifications
  • Previous experience as a Manufacturing Technician or similar role in a cGMP environment.
  • Hands‑on experience with late‑stage floor operations.
  • Ability to work 1st, 2nd, or 3rd shift as needed.
  • Strong attention to detail and adherence to regulated procedures.
  • High school diploma required; technical certificate or degree preferred.
Preferred Skills
  • Experience with electronic batch records or GMP documentation systems.
  • Strong communication and teamwork skills.
  • Ability to work in fast‑paced, highly regulated environments.
  • Contract position with possible extension
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