OSD Manufacturing Technician

Nease Personnel; Greenville (NC); On-site; USD 40,000 - 60,000; Full time

Job summary

JobRx, Inc. is seeking a Pharmaceutical Manufacturing Technician to join our GMP-compliant production team in the Greenville area.

The role focuses on end-to-end production of oral solid dosage products, operating complex machinery and ensuring quality through strict adherence to cGMP and SOP standards. The position requires a high school diploma or equivalent, 1+ year GMP experience, and the ability to obtain forklift certification.

Qualifications

• Education: High School Diploma or equivalent required; technical certification preferred.
• Experience: 1+ years in a GMP pharmaceutical environment; granulation or compression experience preferred.
• Certifications: Ability to obtain internal forklift certification.
• Physical Demands: Lift up to 40 lbs unassisted; stand/walk for shift; respirator medical evaluation; work around chemicals/machinery.

Responsibilities

• Equipment Operation: Setup, operate, teardown, and clean manufacturing machinery (blenders, tablet presses, encapsulators, coaters).
• Production Support: Handle dispensing, sifting, granulation, and compression of materials.
• Documentation: Maintain precise batch logs per cGMP and SOP standards.
• Maintenance & Safety: Monitor equipment, troubleshoot, and enforce PPE and gowning protocols.

Education

High School Diploma or equivalent

Job description

Job Description

Are you a detail-oriented professional with a passion for precision? We are looking for a Pharmaceutical Manufacturing Technician to join a team in the production of high-quality oral solid dosage (OSD) products.

In this role, you will be at the heart of our facility, operating the advanced machinery that transforms raw active ingredients into the life-enhancing tablets and capsules our patients rely on. This isn't just a job on a line; it's a career in a highly regulated, tech-forward environment where your commitment to Current Good Manufacturing Practices (cGMP) ensures the safety and efficacy of every dose.

This role is responsible for the end-to-end production of oral solid dosage (OSD) products in a strictly regulated GMP/FDA environment.

Core Responsibilities

• Equipment Operation: Setup, operate, teardown, and clean manufacturing machinery (blenders, tablet presses, encapsulators, and coaters).
• Production Support: Handle dispensing, sifting, granulation, and compression of materials.
• Documentation: Maintain precise, "right-first-time" records in batch logs per cGMP and SOP standards.
• Maintenance & Safety: Monitor equipment for issues, perform basic troubleshooting, and ensure strict adherence to PPE and gowning protocols.

Job Requirements

• Education: High School Diploma or equivalent (required); Technical certification (preferred).
• Experience: 1+ years in a GMP pharmaceutical environment; specific experience in granulation or compression is highly preferred.
• Certifications: Must be able to obtain an internal forklift certification.
• Physical Demands:
  • Lift up to 40 lbs unassisted; push/pull 100+ lbs.
  • Ability to stand and walk for the majority of the shift.
  • Must pass a medical evaluation to wear a respirator.
  • Comfortable working around chemicals, dust, and moving machinery.

Additional Information

Training will start as first shift (6:00 AM - 4:00 PM) and then transition to second shift (4:00 p.m. - 2:30 a.m.) after training is complete.

MAY WORK FRIDAYS IF THERE IS A BUSINESS NEED.

Successful completion of temporary assignment could result in transition to the company.