Pharmaceutical Production Operator

Umanist Staffing LLC

Chantilly (VA)

On-site

USD 60,000 - 90,000

Full time

6 days ago
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Job summary

Umanist Staffing LLC is seeking experienced Pharmaceutical Production Operators for a full-time role in Chantilly, VA. The position focuses on OSD manufacturing, compression, coating, and related processes in a cGMP/FDA-regulated environment.

The ideal candidate has hands-on experience operating, setting up, cleaning, and troubleshooting pharmaceutical manufacturing equipment, with 3+ years in OSD/Solid Dose production and a strong understanding of cGMP and FDA requirements.

Qualifications

  • OSD / Solid Dose pharmaceutical manufacturing experience is mandatory.
  • Level II requires 3–7 years of pharmaceutical manufacturing experience; Level III requires 7+ years.
  • Hands-on experience operating, setting up, cleaning, and troubleshooting manufacturing equipment in a cGMP/FDA environment.
  • Experience with compression, granulation, encapsulation, coating, or Wurster coating is preferred.

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.

Skills

OSD Manufacturing
Solid Dose
cGMP compliance
FDA compliance

Job description

Position: Pharmaceutical Production Operator II/III — OSD / Compression / Coating
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 escalates 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.
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