Overview
Job Title: Production Operator II / III / Sr. Operator (OSD Manufacturing)
Work Location: Chantilly, VA (Must be willing to relocate to work location)
Employment Type: Full-Time | Onsite
Required Citizenship:
Shifts Available
- 2nd Shift: 4:00 PM – 12:30 AM
- 3rd Shift: 12:00 AM – 8:30 AM
- (Must be flexible to work overtime when required)
About the Role
We are hiring experienced Production Operators (II/III/Senior) with Oral Solid Dosage (OSD) manufacturing experience to join our growing team in Chantilly, VA. In this role, you will be responsible for operating, cleaning, and maintaining pharmaceutical manufacturing equipment while ensuring compliance with Good Manufacturing Practices (cGMP) and company Standard Operating Procedures (SOPs).
You will work on processes such as Compression, Coating, Granulation, and Encapsulation, supporting production goals while upholding the highest safety and quality standards.
Key Responsibilities
- Operate, clean, and set up pharmaceutical production equipment (e.g., tablet press, encapsulation, fluid bed dryers, granulation, coating).
- Execute written SOPs and ensure product compliance with cGMP requirements.
- Perform machine changeovers, in-process checks, and batch documentation accurately.
- Inspect raw materials, verify product ID labels, and maintain proper documentation.
- Support troubleshooting of equipment and process-related issues.
- Participate in continuous improvement projects to enhance efficiency and quality.
- Maintain a clean and safe work environment, following OSHA and company safety standards.
- Collaborate with cross-functional teams to meet production schedules and goals.
Qualifications
- Must have Oral Solid Dosage (OSD) manufacturing experience.
- Experience in one or more of the following: Compression, Granulation, Encapsulation, Coating, Wurster Coating, Fluid Bed Dryers, Bead Tower.
- Proficiency in cleaning, dismantling, and operating state-of-the-art equipment such as: Fette 3200i, Fette P 3030, MG2 Planeta, Korsch XM 12, Glatt systems
- Knowledge of cGMP standards, FDA regulations, and SOP compliance
- Ability to lift up to 50 lbs, stand for extended periods, and wear PPE.
- High School Diploma or GED required; Associate’s Degree preferred.
- Level II: 2–5 years of pharma manufacturing experience
- Level III/Senior: 5+ years of pharma manufacturing experience
- Competitive hourly pay
- Full healthcare coverage (Medical, Dental, Vision)
- 401(k) with company match
- Paid Time Off (PTO), sick leave, and holidays
- Relocation support & temporary accommodation available
- Career growth in a cGMP-regulated environment
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