Production Operator II/III; Relocate to Virginia,
Listed on 2026-06-16
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Manufacturing / Production
Pharmaceutical Manufacturing, Validation Engineer, Quality Engineering, Operations Engineer -
Pharmaceutical
Pharmaceutical Manufacturing, Validation Engineer, Quality Engineering
Production Operator II / III – OSD Pharmaceutical Manufacturing
Relocation Opportunity to Chantilly, Virginia, USA
Open to Canadian Citizens Eligible for TN Visa Sponsorship
Full-Time | In office | Multiple Shifts Available
Relocation assistance and temporary accommodation support are available for qualified candidates relocating to Virginia.
Candidates must be flexible for overtime and shift schedules:
- 2nd Shift: 4:00PM – 12:30AM
- 3rd Shift: 12:00AM – 8:30AM
Are you an experienced pharmaceutical manufacturing professional looking for an opportunity to grow your career in the United States?
We are actively hiring skilled Oral Solid Dosage (OSD) Manufacturing Operators from Canada who are interested in relocating to Virginia under the TN Visa program.
This is an excellent opportunity to join a modern pharmaceutical manufacturing environment offering relocation support, strong benefits, career growth, and exposure to advanced manufacturing technologies.
Position OverviewWe are seeking experienced Production Operators Level
II &III with strong hands‑on experience in Oral Solid Dosage (OSD) pharmaceutical manufacturing environments.
- Compression
- Granulation
- Encapsulation (Hard‑Gel)
- Coating
- Wurster Coating
- Fluid Bed Dryers
- Bead Tower
- Tablet Printing / Ackley Laser Drill
- Operate pharmaceutical manufacturing equipment in a cGMP environment
- Perform equipment setup, cleaning, dismantling, and changeovers
- Execute manufacturing processes according to SOPs and batch records
- Conduct in‑process quality checks and documentation
- Troubleshoot equipment and process issues
- Maintain compliance with FDA and cGMP regulations
- Support continuous improvement and operational excellence initiatives
- Ensure safety, quality, and productivity standards are consistently met
Level
II Operator
Minimum 3–7 years of OSD pharmaceutical manufacturing experience
LevelIII Operator
Minimum 7+ years of pharmaceutical manufacturing experience
Must‑Have Experience- Strong Oral Solid Dosage (OSD) manufacturing background
- Experience with Compression, Granulation, Encapsulation, or Coating operations
- Fette 3200i
- Fette P3030
- MG2 Planeta
- Korsch XM12
- FDA regulations
- cGMP
- Lean Manufacturing
- Six Sigma
- Tablet Compression
- Hard‑Gel Encapsulation
- Granulation
- Coating
- Wurster Coating
- Fluid Bed Processing
- Relocation assistance
- Temporary accommodation support
- Medical, Dental & Vision benefits
- 401(k) matching
- Paid time off & holidays
- Long‑term career growth opportunities
Drug screen and background check required after offer stage.
Skills- OSD Manufacturing
- Tablet Compression
- Granulation
- Encapsulation
- Pharmaceutical Manufacturing
- cGMP
- FDA Compliance
- Coating
- Wurster Coating
- Fluid Bed Dryer
- Lean Manufacturing
- Six Sigma
- Fette
- MG2
- Korsch XM12
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