Pharmaceutical Manufacturing Operator Job Township of Cranbury New Jersey USA,Manufacturing / Production

Location: Township of Cranbury

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