GMP Pharmaceutical Technician I — Solid Dose Manufacturing

Catalent Pharma Solutions; South Carolina; On-site; USD 42,000 - 62,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

Tuition Reimbursement

Paid time off

Onsite wellness programs

Job summary

Catalent is seeking a Pharmaceutical Technician I to support GMP manufacturing for oral solid dose products at our Greenville, NC site. The role covers dispensing, compounding, compressing, encapsulating, coating, and printing with supervision.

You will assemble, disassemble, and clean equipment, assist with troubleshooting, and ensure accurate documentation in line with SOPs and FDA cGMP. Shift: M-F, 2nd Shift; 100% onsite with opportunities for growth in a fast-paced, compliant environment

Qualifications

• High school diploma or equivalent with at least 2 years of experience in pharmaceutical oral solid dose manufacturing.
• Associate degree with at least 1 year of experience in pharmaceutical oral solid dose manufacturing.
• Required to obtain internal forklift operation certification.

Responsibilities

• Perform GMP manufacturing operations in an oral solid dose environment, including dispensing, compounding, compressing, encapsulating, coating, and printing, with minimal supervision.
• Assemble, disassemble, clean and store manufacturing equipment.
• Assist with troubleshooting machinery and equipment and recommend corrective or preventative measures.
• Ensure all batch records and logbook entries are accurately documented and compliant with SOPs and FDA cGMP guidelines.
• With minimal supervision, conduct setup, changeover, and manufacturing activities with adherence to SOPs and safety requirements.
• All Other Duties as assigned

Skills

GMP manufacturing

Oral solid dose

Documentation

Troubleshooting

Safety compliance

Education

High school diploma or equivalent

Associate degree

Tools

Forklift certification

Job description

Catalent is seeking a Pharmaceutical Technician I to support GMP manufacturing for oral solid dose products at our Greenville, NC site. The role covers dispensing, compounding, compressing, encapsulating, coating, and printing with supervision.

You will assemble, disassemble, and clean equipment, assist with troubleshooting, and ensure accurate documentation in line with SOPs and FDA cGMP. Shift: M-F, 2nd Shift; 100% onsite with opportunities for growth in a fast-paced, compliant environment