Solid Dosage Pharma Operator - GMP Manufacturing Pro

Cephas Consultancy Services Private Limited; Cranbury Township (NJ); On-site; USD 40,000 - 60,000; Full time

Job summary

Cephas Consultancy Services Private Limited in Cranbury, New Jersey, United States, is seeking a Production Operator for solid-dosage pharmaceutical manufacturing. The role covers dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and related documentation in English.

Ideal candidates will have 2–15 years of experience in regulated pharmaceutical production, familiarity with cGMP equipment, and the ability to work with minimal supervision while adhering to

Qualifications

• Familiarity with working in a regulated pharmaceutical solid dosage facility.
• Reading and writing documents in English.
• Familiarity with cGMP solid dosage manufacturing equipment.
• Ability to work with minimal supervision.
• Ability to stand for an 8-hour shift.
• Ability to lift up to 30 lbs (14 kg).
• Maintain hygiene in a cGMP environment.
• Capable of wearing PPE per OSHA guidelines.

Responsibilities

• Assist Production Management with scheduled and requested activities.
• Ensure manufacturing activities are completed on time.
• Set up, operate, and clean cGMP equipment used in production.
• Participate in Quality Investigations as required.
• Follow SOPs, Batch Records and Safety Procedures.
• Maintain clean cGMP area and good housekeeping.
• Wear required PPE during cGMP activities.

Skills

Regulated pharmaceutical environment

Reading & writing English

cGMP equipment familiarity

Self-supervision

Eight-hour stamina

Lifting up to 14 kg

Personal hygiene in cGMP

PPE usage

Education

High School Diploma or GED

Bachelor’s in Physical Sciences or pharmaceutical life science

Job description

Cephas Consultancy Services Private Limited in Cranbury, New Jersey, United States, is seeking a Production Operator for solid-dosage pharmaceutical manufacturing. The role covers dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and related documentation in English.

Ideal candidates will have 2–15 years of experience in regulated pharmaceutical production, familiarity with cGMP equipment, and the ability to work with minimal supervision while adhering to