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Production Operator Ii Iii

  • ... Posted on: Nov 04, 2025
  • ... Unizontechnology
  • ... Chantilly, Virginia
  • ... Salary: Not Available
  • ... Full-time

Production Operator Ii Iii   

Job Title :

Production Operator Ii Iii

Job Type :

Full-time

Job Location :

Chantilly Virginia United States

Remote :

No

Jobcon Logo Job Description :

Job Summary (List Format) Production Operator II / III Oral Solid Dosage (OSD)

- Operate, set up, clean, and maintain pharmaceutical manufacturing equipment for OSD processes (compression, coating, granulation, encapsulation, blending, drying)
- Follow cGMPs and SOPs to ensure compliance with FDA and company quality standards
- Weigh, blend, dispense, and process raw materials per batch records
- Conduct in-process quality checks and maintain accurate production documentation
- Perform equipment changeovers, troubleshooting, and routine maintenance
- Participate in continuous improvement initiatives for safety, efficiency, and quality
- Maintain cleanliness and organization of the manufacturing area
- Support adherence to safety standards (FDA, OSHA, company policies)
- Work full-time on 2nd or 3rd shift; flexible to work overtime as needed
- Requires hands-on OSD/pharmaceutical manufacturing experience and physical ability for manual tasks
- Opportunities for growth, relocation support, and comprehensive benefits available

Let me know if you need a shorter or more detailed summary!

Jobcon Logo Position Details

Posted:

Nov 04, 2025

Employment:

Full-time

Salary:

Not Available

Snaprecruit ID:

SD-CIE-cca4fe310a6051e20b726089e2e95489142edba39f360b41e66c2ee8ee03eb47

City:

Chantilly

Job Origin:

CIEPAL_ORGANIC_FEED

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Job Summary (List Format) Production Operator II / III Oral Solid Dosage (OSD)

- Operate, set up, clean, and maintain pharmaceutical manufacturing equipment for OSD processes (compression, coating, granulation, encapsulation, blending, drying)
- Follow cGMPs and SOPs to ensure compliance with FDA and company quality standards
- Weigh, blend, dispense, and process raw materials per batch records
- Conduct in-process quality checks and maintain accurate production documentation
- Perform equipment changeovers, troubleshooting, and routine maintenance
- Participate in continuous improvement initiatives for safety, efficiency, and quality
- Maintain cleanliness and organization of the manufacturing area
- Support adherence to safety standards (FDA, OSHA, company policies)
- Work full-time on 2nd or 3rd shift; flexible to work overtime as needed
- Requires hands-on OSD/pharmaceutical manufacturing experience and physical ability for manual tasks
- Opportunities for growth, relocation support, and comprehensive benefits available

Let me know if you need a shorter or more detailed summary!

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