Pharmaceutical Manufacturing Operator

Pharmaceutical Manufacturing Operator – Oral Solid Dosage (OSD)

Job Type: Full-Time
Industry: Pharmaceutical Manufacturing
Experience: OSD Pharmaceutical Manufacturing Experience Required

Job Summary

We are seeking an experienced Pharmaceutical Manufacturing Operator with hands-on experience in Oral Solid Dosage (OSD) pharmaceutical manufacturing.

The ideal candidate will have practical experience operating, setting up, cleaning, and troubleshooting cGMP manufacturing equipment, with strong hands-on experience in tablet compression and granulation.

Mandatory Requirements

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  Must have hands-on experience in Oral Solid Dosage (OSD) pharmaceutical manufacturing

  
  


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  Hands-on Tablet Compression experience, including:

  
  
  
  
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    Tablet press setup

    
    
  
  
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    Equipment operation

    
    
  
  
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    In-process checks

    
    
  
  
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    Troubleshooting

    
    
  
  
  
  


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  Hands-on Granulation experience, including:

  
  
  
  
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    Wet or dry granulation

    
    
  
  
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    Equipment setup and operation

    
    
  
  
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    Troubleshooting

    
    
  
  
  
  


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  Must have worked in an actual cGMP-regulated pharmaceutical solid dosage manufacturing facility

  
  


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  Must be able to read, understand, and complete documentation in English

  
  


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  High School Diploma/GED required

  
  


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  Bachelor's degree in Physical Sciences, Pharmaceutical Sciences, Life Sciences, or related field preferred/required based on company requirements

  
  

Key Responsibilities

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  Execute commercial and non-commercial OSD manufacturing activities according to production schedules.

  
  


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  Set up, operate, clean, and troubleshoot cGMP pharmaceutical manufacturing equipment.

  
  


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  Perform activities related to dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and cleaning.

  
  


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  Complete batch records and other cGMP documentation accurately, thoroughly, and legibly.

  
  


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  Follow approved SOPs, batch records, safety procedures, and PPE requirements.

  
  


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  Perform required in-process checks during manufacturing.

  
  


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  Participate in Quality Investigations as required.

  
  


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  Maintain cleanliness and good housekeeping within cGMP manufacturing areas.

  
  


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  Work closely with Production Management, Quality, Engineering, and other site support personnel.

  
  


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  Complete scheduled manufacturing activities safely, efficiently, and on time.

  
  


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  Work independently with minimal supervision.