Production Operator II/III; Relocate to Virginia,
Job in
Bas-St-Laurent-Est (Sainte-Luce), Province de Québec, G0K, Canada
Listed on 2026-05-31
Listing for:
Bilinguallink
Full Time
position Listed on 2026-05-31
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Quality Engineering, Validation Engineer -
Pharmaceutical
Pharmaceutical Manufacturing, Quality Engineering, Validation Engineer
Job Description & How to Apply Below
Location: Bas-St-Laurent-Est (Sainte-Luce)
Production Operator II / III – OSD Pharmaceutical Manufacturing
Open to Canadian Citizens Eligible for TN Visa Sponsorship
Full-Time | On-site | Multiple Shifts Available
Relocation assistance and temporary accommodation support are available for qualified candidates relocating to Virginia.
Shift Availability
2nd
Shift: 4:00 PM – 12:30 AM
3rd
Shift: 12:00 AM – 8:30 AM
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 Overview
We are seeking experienced Production Operators Level II & III with strong hands‑on experience in Oral Solid Dosage (OSD) pharmaceutical manufacturing environments.
Candidates should have experience in one or more of the following areas:
Compression | Granulation | Encapsulation (Hard-Gel) | Coating | Wurster Coating | Fluid Bed Dryers | Bead Tower | Tablet Printing / Ackley Laser Drill
Key Responsibilities
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
Required Qualifications
Level II Operator
Minimum 3–7 years of OSD pharmaceutical manufacturing experience
Level III 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
Hands‑on experience with equipment such as:
Fette 3200i
Fette P3030
MG2 Planeta
Korsch XM 12
Knowledge of:
FDA regulations
cGMP
Lean Manufacturing
Six Sigma
Ability to independently operate, clean, set up, and dismantle pharmaceutical manufacturing equipment.
We are specifically seeking candidates with:
Tablet Compression
Hard‑Gel Encapsulation
Granulation
Coating
Wurster Coating
Fluid Bed Processing experience
Compensation & Benefits
Relocation assistance
Temporary accommodation support
Medical, Dental & Vision benefits
401(k) matching
Paid time off & holidays
Long‑term career growth opportunities
Interview Process
Virtual MS Teams Interview
On‑site Interview Visit
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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