Production Operator

Inteletech Global Inc; Chantilly (VA); On-site; USD 47,000 - 70,000; Full time

Benefits offered by this job

Relocation support

Healthcare benefits

401(k) matching

Paid time off (PTO)

Job summary

A leading pharmaceutical company in Chantilly, Virginia, seeks Production Operators (Level II/III/Senior) for its manufacturing facility. The ideal candidates will have hands-on experience with OSD processes and knowledge of cGMP. Key responsibilities include operating specialized equipment, ensuring compliance, and maintaining documentation. Benefits include relocation support, healthcare coverage, and retirement plans. Join us in delivering high-quality pharmaceutical products to improve patient health and well-being.

Qualifications

• Hands-on experience operating and maintaining pharmaceutical equipment in a cGMP-regulated environment.
• 2–5 years experience for Level II, or 5+ years for Level III in pharmaceutical manufacturing.

Responsibilities

• Operate equipment for Compression, Granulation, Coating, Encapsulation, and Fluid Bed Drying.
• Complete batch records and ensure workspace compliance.
• Participate in continuous improvement projects.

Skills

OSD manufacturing experience

Knowledge of Good Manufacturing Practices (cGMP)

Basic English communication skills

Ability to work overtime

Education

High School Diploma, GED, or Associate Degree

Tools

Fette 3200i

MG2 Planeta

Korsch XM 12

Job description

Job Title: Production Operator II / III / Sr. Operator

Location: Chantilly, Virginia, USA

Positions: 10

Job Type: Full-Time

Salary Range: $47,000 - $70,000 annually ($23 - $35/hour)

Shift Availability: 2nd (4:00pm – 12:30am) & 3rd (12:00am – 8:30am)

Work Authorization: U.S. Citizen or Permanent Resident only

Job Summary

Granules Pharmaceuticals is hiring Production Operators (Level II/III/Senior) for its Oral Solid Dosage (OSD) manufacturing facility in Chantilly, VA. The ideal candidate will have hands‑on experience operating and maintaining state‑of‑the‑ pharmaceutical equipment in a cGMP‑regulated environment.

Key Responsibilities

• Operate equipment for processes such as Compression, Granulation, Coating, Encapsulation, Wurster Coating, and Fluid Bed Drying.
• Perform equipment setup, operation, cleaning, and dismantling.
• Follow cGMPs, SOPs, and FDA regulatory guidelines.
• Accurately complete batch records, logbooks, and production documentation.
• Sample and inspect product batches.
• Maintain a clean, safe, and compliant workspace.
• Participate in continuous improvement projects and cross‑functional collaboration.
• Troubleshoot and upscale process/equipment issues.

Must‑Have Qualifications

• OSD manufacturing experience is required.
• Knowledge of Good Manufacturing Practices (cGMP).
• Experience with tablet presses and encapsulation equipment:
  • Fette 3200i / P 3030
  • MG2 Planeta
  • Korsch XM 12
• Hands‑on expertise in one or more of the following: Compression, Granulation, Encapsulation, Coating, Wurster Coating, Bead Towers, Fluid Bed Dryers.
• Basic English communication skills (reading/speaking).
• Ability to work overtime and different shifts as needed.

Preferred Qualifications

• Familiarity with Lean Manufacturing, Six Sigma practices.
• Experience working with potent compounds.
• Forklift certification (may be required for certain roles).
• High School Diploma, GED, or Associate Degree.
• 2–5 years (Level II) or 5+ years (Level III) of experience in pharmaceutical manufacturing.

Physical Requirements

• Must stand for extended periods (up to 12 hours).
• Able to lift/move 50 lbs, climb ladders, wear respirators/PPE.
• Work in regulated environments (lab/manufacturing areas).
• Relocation support and temporary accommodation.
• Full‑time healthcare benefits, 401(k) matching, PTO.
• Drug screening & background check post‑offer.

Benefits

• Relocation support and temporary accommodation.
• Full‑time healthcare benefits.
• 401(k) matching.
• Paid time off (PTO).
• Drug screening & background check post‑offer.