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Pharmaceutical Manufacturing Operator

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Onsite

Pharmaceutical Manufacturing Operator

Umanist

Pharmaceutical Manufacturing Operator

1 month ago

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Important information


Contract type:

Permanent

Location:

New Jersey, USA

Work mode:

Onsite

Published on:

24 September 2026

What they need


Pharmaceutical Manufacturing Operator – Oral Solid Dosage (OSD)

Job Type: Full-Time
Industry: Pharmaceutical Manufacturing
Experience: OSD Pharmaceutical Manufacturing Experience Required

Job Summary

We are seeking an experienced Pharmaceutical Manufacturing Operator with hands-on experience in Oral Solid Dosage (OSD) pharmaceutical manufacturing.

The ideal candidate will have practical experience operating, setting up, cleaning, and troubleshooting cGMP manufacturing equipment, with strong hands-on experience in tablet compression and granulation.

Mandatory Requirements

  • Must have hands-on experience in Oral Solid Dosage (OSD) pharmaceutical manufacturing
  • Hands-on Tablet Compression experience, including:
    • Tablet press setup
    • Equipment operation
    • In-process checks
    • Troubleshooting
  • Hands-on Granulation experience, including:
    • Wet or dry granulation
    • Equipment setup and operation
    • Troubleshooting
  • Must have worked in an actual cGMP-regulated pharmaceutical solid dosage manufacturing facility
  • Must be able to read, understand, and complete documentation in English
  • High School Diploma/GED required
  • Bachelor's degree in Physical Sciences, Pharmaceutical Sciences, Life Sciences, or related field preferred/required based on company requirements

Key Responsibilities

  • Execute commercial and non-commercial OSD manufacturing activities according to production schedules.
  • Set up, operate, clean, and troubleshoot cGMP pharmaceutical manufacturing equipment.
  • Perform activities related to dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and cleaning.
  • Complete batch records and other cGMP documentation accurately, thoroughly, and legibly.
  • Follow approved SOPs, batch records, safety procedures, and PPE requirements.
  • Perform required in-process checks during manufacturing.
  • Participate in Quality Investigations as required.
  • Maintain cleanliness and good housekeeping within cGMP manufacturing areas.
  • Work closely with Production Management, Quality, Engineering, and other site support personnel.
  • Complete scheduled manufacturing activities safely, efficiently, and on time.
  • Work independently with minimal supervision.

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