OSD Solid-Dose Production Operator II/III

Umanist Staffing LLC; Chantilly (VA); On-site; USD 60,000 - 90,000; Full time

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 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.