Pharma Quality Auditor — GMP & ISO Focus

West Pharmaceutical Services, Inc

Cidra (PR)

Hybrid

USD 52,000 - 76,000

Full time

13 days ago

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Benefits offered by this job

Generous PTO
Recognition & Rewards
Inclusive culture
Learning & development
Global career opportunities
Community involvement

Job summary

West Pharmaceutical Services, Inc in Cidra, PR is seeking a Quality Auditor to ensure in-process and finished goods meet specifications. The role performs quality inspection, control, sampling, documentation and GDP-compliant record keeping in a cGMP environment.

The position requires a high school diploma (associate degree preferred) and 1+ year of relevant experience; strong attention to detail and basic computer skills are essential. Shift: 12-hour, 2-2-3 rotation.

Qualifications

  • High school diploma or GED required.
  • Associate degree in Science, Math, or related field preferred.
  • 1+ year in a cGMP environment preferred.

Responsibilities

  • Perform sampling, inspections, and testing of in-process and finished goods.
  • Release acceptable products for processing or shipping.
  • Understand and follow ISO standards requirements.
  • Review inspection records for conformance and proper documentation.
  • Retain samples and maintain batch records and disposition.
  • Print documents and manage Quality System records.
  • Segregate nonconforming product and quarantine materials.
  • Generate rejection and deviation reports as directed.
  • Conduct trace-back investigations of nonconforming material.
  • Promote and support a Lean environment.
  • Adhere to safety rules and maintain attendance.

Skills

Attention to detail
Basic computer skills
AQL knowledge
ShopFloor experience

Education

High school diploma or GED
Associate degree preferred

Job description

West Pharmaceutical Services, Inc in Cidra, PR is seeking a Quality Auditor to ensure in-process and finished goods meet specifications. The role performs quality inspection, control, sampling, documentation and GDP-compliant record keeping in a cGMP environment.

The position requires a high school diploma (associate degree preferred) and 1+ year of relevant experience; strong attention to detail and basic computer skills are essential. Shift: 12-hour, 2-2-3 rotation.

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