OSD Manufacturing Technician

Nease Personnel

Greenville (NC)

Vor Ort

USD 40.000 - 60.000

Vollzeit

14 Tage+

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Zusammenfassung

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.

Qualifikationen

  • 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.

Aufgaben

  • 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.

Ausbildung

High School Diploma or equivalent

Jobbeschreibung

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.

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