Jobs · Management · Virginia

Pharmaceutical Production Operator

Umanist NA · Chantilly, VA · 1 mo ago
On-siteManagementFull-time

Location: Chantilly, VA

Job Type: Full-Time

Experience: 3+ years OSD/Solid Dose Pharmaceutical Manufacturing

Job Summary

We are seeking experienced Pharmaceutical Production Operators with hands‑on OSD (Oral Solid Dose) / solid‑dose manufacturing experience. The ideal candidate will have direct experience operating, setting up, cleaning, and troubleshooting pharmaceutical manufacturing equipment in a cGMP/FDA‑regulated environment. Candidates with experience in Compression, Granulation, Encapsulation, Coating, or Wurster Coating are encouraged to apply. Soft‑gel‑only manufacturing experience will not be considered.

Key Responsibilities

  • Operate pharmaceutical manufacturing equipment according to SOPs and cGMP requirements.
  • Perform weighing, dispensing, blending, granulation, drying, milling, compression, encapsulation, and/or coating processes.
  • Set up, clean, dismantle, and operate production equipment.
  • Perform equipment changeovers between batches.
  • Complete Batch Production Records, logbooks, and other manufacturing documentation accurately.
  • Perform in‑process quality checks and batch sampling.
  • Troubleshoot manufacturing/process issues and escalate deviations appropriately.
  • Verify raw materials, labels, QC release tags, and batch documentation before production.
  • Maintain a clean and organized manufacturing area.
  • Participate in continuous improvement and safety initiatives.
  • Follow all FDA, cGMP, SOP, safety, and company requirements.

Required Experience

  • OSD / Solid Dose pharmaceutical manufacturing experience is mandatory.
  • Level II: 3–7 years of pharmaceutical manufacturing experience.
  • Level III: 7+ years of pharmaceutical manufacturing experience.
  • Hands‑on experience in at least one of the following: Compression, Granulation, Encapsulation, Coating, Wurster Coating, Tablet Printing / Ackley Laser Drill, Fluid Bed Dryers, Bead Tower.
  • Strong understanding of cGMP and FDA requirements.
  • Ability to follow SOPs and accurately complete batch documentation.
  • Ability to clean, set up, dismantle, and operate pharmaceutical manufacturing equipment.

Skills

  • Compression
  • Granulation
  • Encapsulation
  • OSD processes
  • Documentation
  • Deviations handling
  • In‑process checks
  • Continuous improvement
  • Pharmaceutical manufacturing

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