Pharmaceutical Manufacturing Operator

Umanist; Cranbury Township (NJ); On-site; USD 52,000 - 76,000; Full time

Job summary

Umanist is seeking an experienced Pharmaceutical Manufacturing Operator for Oral Solid Dosage (OSD) operations. The role requires hands-on work with tablet compression and granulation in a cGMP environment.

The ideal candidate will read and complete documentation in English, and hold a High School Diploma/GED with a degree in Physical/Life Sciences preferred. On-site duties include setup, operation, cleaning, troubleshooting, and batch record completion.

Qualifications

• Must have hands-on experience in OSD manufacturing.
• Experience with tablet compression and granulation.
• Read and complete documentation in English.
• Experience in a cGMP-regulated facility.
• High School Diploma/GED required; degree preferred.

Responsibilities

• Execute commercial and non-commercial OSD manufacturing activities per production schedules.
• Set up, operate, clean, and troubleshoot cGMP manufacturing equipment.
• Perform dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and cleaning tasks.
• Complete batch records and cGMP documentation accurately.
• Follow SOPs, batch records, safety procedures, and PPE requirements.
• Conduct in-process checks during manufacturing and support quality investigations.
• Maintain cleanliness and good housekeeping in cGMP areas.
• Collaborate with Production Management, Quality, Engineering, and site support.
• Complete scheduled activities safely, efficiently, and on time.
• Work independently with minimal supervision.

Skills

OSD manufacturing experience

Tablet compression

Granulation

cGMP environment

English literacy

Diploma/GED

Education

High School Diploma/GED

Bachelor’s in Physical/Life Sciences

Tools

Tablet press equipment

Granulation equipment

Coating/drying equipment

cGMP documentation handling

Job description

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.