Pharmaceutical Production Operator – OSD

Elvis Eckardt Recruitment; Sully Square (VA); On-site; USD 47,000 - 70,000; Full time

Job summary

Elvis Eckardt Recruitment is hiring a Pharmaceutical Production Operator for their Chantilly, VA facility. The role involves operating advanced production equipment in a cGMP environment, ensuring quality compliance, and participating in continuous improvement initiatives. Ideal candidates have 3–7 years of experience in solid dosage manufacturing and a strong understanding of regulatory requirements.

Benefits

401(k)

Qualifications

• 3–7 years of experience in OSD manufacturing required.
• Strong understanding of cGMP regulations and compliance.
• Ability to lift 50 lbs and work in PPE.

Responsibilities

• Operate and maintain pharmaceutical production equipment.
• Complete documentation and ensure compliance with safety standards.
• Engage in continuous improvement projects and teamwork.

Skills

Knowledge of manufacturing processes

Attention to detail

Strong verbal communication

Education

Minimum 3–7 years of experience in solid dosage pharmaceutical manufacturing

Tools

Fette 3200i

Fette P3030

MG2 Planeta

Korsch XM12

Job description

Pharmaceutical Production Operator – OSD

Pharmaceutical Production Operator – OSD

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Elvis Eckardt Recruitment provided pay range

This range is provided by Elvis Eckardt Recruitment. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$47,000.00/yr - $70,000.00/yr

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Entrepreneur & Founder | Robin Hood meets Recruitment | Fractional TA Leader | Moonshot | Father to a cheeky | Extended Workbench for the Big 4…

Job Title: Pharmaceutical Production Operator – OSD

Location: Chantilly, VA

Job Type: Full-time

Industry: Pharmaceutical Manufacturing

Position Overview:

We are hiring experienced Pharmaceutical Production Operators – OSD with a solid background in Oral Solid Dosage (OSD) manufacturing.

In this role, you will operate pharmaceutical production equipment, perform in-process quality checks, and ensure compliance with cGMP regulations and SOPs. This is a hands-on, team-oriented role in a fast-paced and highly regulated environment.

Key Responsibilities:

Manufacturing Operations

• Operate and maintain pharmaceutical production equipment for weighing, blending, granulation, drying, milling, compression, encapsulation, and coating.
• Perform changeovers and clean equipment according to established SOPs.
• Verify and stage raw materials, ensuring correct identification and documentation.
• Perform in-process checks and ensure adherence to production schedules and routers.
• Sample batches for QA testing as needed.

Documentation & Compliance

• Accurately complete batch records, logbooks, weight tickets, and related documentation.
• Ensure all documentation meets cGMP and company quality standards.
• Update production boards and participate in operational debriefs.
• Participate in troubleshooting and minor maintenance of equipment.
• Engage in lean initiatives and continuous improvement projects.
• Collaborate with cross-functional teams to meet production and quality targets.

Safety & Housekeeping

• Follow all safety protocols, wear required PPE, and maintain a clean and safe workspace.
• Participate in safety discussions, incident reviews, and start-up meetings.

Qualifications & Experience:

• Minimum 3–7 years of experience in solid dosage pharmaceutical manufacturing under cGMP.
• Strong knowledge of manufacturing processes and OSD equipment.

Technical Requirements:

• Solid experience with equipment such as Fette 3200i, Fette P3030, MG2 Planeta, and Korsch XM12.
• Proficiency in operations including Compression, Granulation, Encapsulation, Wurster Coating, Fluid Bed Drying, and Bead Towers.
• Familiarity with FDA regulations, GMP, Lean Manufacturing, and Six Sigma principles.
• Basic math, mechanical aptitude, and computer literacy.

Physical Requirements:

• Ability to stand for extended periods (up to 12 hours).
• Must be able to lift 50 lbs, climb ladders, and work in PPE, including respirators, safety glasses, and steel-toed shoes.

Preferred Skills:

• Forklift certification (may be required for some positions).
• Strong written and verbal communication.
• Commitment to accuracy, safety, and quality.

Shift Options:

• 1st Shift: 7:00 AM – 3:30 PM EST
• 2nd Shift: 3:00 PM – 11:30 PM EST

Must be available for initial training: Monday–Friday, 8:30 AM – 5:00 PM for approximately 1 month

Apply now to join a mission-driven team producing high-quality solid dosage pharmaceuticals in a world-class cGMP facility.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Production and Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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Inferred from the description for this job

401(k)

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