Pharma Manufacturing Operator III - Solid Dose Expert

Gregory Pharmaceutical Holdings Inc

Bristol (TN)

On-site

USD 25,000 - 36,000

Full time

9 days ago

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Job summary

Gregory Pharmaceutical Holdings Inc is seeking a Manufacturing Operator III to join the Bristol, TN manufacturing team. You will perform manufacturing processes for solid dose tablets, capsules, and liquid dose forms in accordance with SOPs, batch records, and cGMP procedures.

Responsibilities include setting up and operating equipment, conducting in-process tests, maintaining batch records and logs, cleaning, troubleshooting, and supporting training and quality initiatives within a fast-paced

Qualifications

  • 10 years experience in a manufacturing/packaging environment, or 7 years of applicable pharmaceutical experience.
  • High School diploma or GED is required.
  • Experience with solid dose and semi-solid manufacturing equipment desirable.
  • Ability to read and interpret safety rules, SOPs, batch records.

Responsibilities

  • Weighs and samples development and commercial manufacturing batches per SOPs.
  • Sets up, operates, breaks down and cleans equipment per SOPs and equipment specs.
  • Performs scheduled manufacturing activities per approved batch records.
  • Performs in-process and verification tests during manufacturing.
  • Maintains batch records, equipment and room use logs, and inventory records per SOPs.
  • Cleans equipment and facility per SOPs and cGMP procedures.
  • Troubleshoots equipment during manufacturing.
  • Provides departmental training on equipment and processes.
  • Performs other duties as assigned.

Skills

cGMP compliance
Equipment operation
Documentation
Safety and quality

Education

High School diploma or GED

Tools

Tablet presses
Encapsulators
Fluid bed systems
Blending equipment
Spray coaters

Job description

Gregory Pharmaceutical Holdings Inc is seeking a Manufacturing Operator III to join the Bristol, TN manufacturing team. You will perform manufacturing processes for solid dose tablets, capsules, and liquid dose forms in accordance with SOPs, batch records, and cGMP procedures.

Responsibilities include setting up and operating equipment, conducting in-process tests, maintaining batch records and logs, cleaning, troubleshooting, and supporting training and quality initiatives within a fast-paced

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