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Production Operator II​/III; Relocate to Virginia,

Job in Bas-St-Laurent-Est (Sainte-Luce), Province de Québec, G0K, Canada
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
Position: Production Operator II / III (Relocate to Virginia, USA)
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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