Pharmaceutical Manufacturing Operator

Umanist NA; Cranbury Township (NJ); On-site; USD 65,000 - 90,000; Full time

Job summary

Umanist NA is seeking an experienced Pharmaceutical Manufacturing Operator specializing in Oral Solid Dosage (OSD) production. The role requires hands-on operation, setup, cleaning, and troubleshooting of cGMP equipment with emphasis on tablet compression and granulation.

The ideal candidate will perform dispensing, granulation, sifting, milling, drying, encapsulation, coating, and compression while maintaining strict batch records and documentation in English.

Qualifications

• Hands-on experience in Oral Solid Dosage (OSD) pharmaceutical manufacturing.
• Experience with tablet compression and granulation processes.
• Ability to read, understand, and complete cGMP documentation in English.

Responsibilities

• Execute OSD manufacturing activities according to production schedules.
• Set up, operate, clean, and troubleshoot cGMP equipment.
• Perform dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and cleaning tasks.
• Complete batch records and other cGMP documentation accurately.
• Follow SOPs, batch records, safety procedures, and PPE requirements.
• Perform in-process checks during manufacturing.
• Participate in Quality Investigations as required.
• Maintain cleanliness and good housekeeping in cGMP areas.
• Work with Production Management, Quality, Engineering, and site support.

Skills

documentation

granulation

pharmaceutical manufacturing

troubleshooting

manufacturing

batch records

checks

osd

cgmp manufacturing

compression

Education

High School Diploma/GED

Bachelor's degree in Physical Sciences, Pharmaceutical Sciences, Life Sciences, or related field

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.

Skills: documentation,granulation,pharmaceutical manufacturing,troubleshooting,manufacturing,batch records,checks,osd,cgmp manufacturing,compression