Ingénieur Aq Operationnelle H/f - Cdd De 4 Mois

GlaxoSmithKline

Evreux, France
Good manufacturing practices compliance
Batch release review and approval
Deviation and incident investigations
The role involves ensuring operational quality on the production floor to guarantee manufacturing compliance with Good Manufacturing Practices

Job Summary

  • The role involves ensuring operational quality on the production floor to guarantee manufacturing compliance with Good Manufacturing Practices.
  • Candidates will be responsible for revising and contributing to batch releases within their delegated scope while managing deviations and out-of-specification results.
  • GSK Evreux is a major pharmaceutical site producing respiratory medications, employing approximately 1,000 people and contributing significantly to the company's global revenue.

Matching Summary

The role involves ensuring operational quality on the production floor to guarantee manufacturing compliance with Good Manufacturing Practices.

Skills & Requirements

Must-have

  • Good Manufacturing Practices compliance
  • Batch release review and approval
  • Deviation and incident investigations
  • CAPA tracking and verification
  • On-site quality surveillance

Nice-to-have

  • Internal audit experience
  • Regulatory inspection preparation
  • Continuous improvement projects
  • Data analysis skills
  • Veeva or SAP knowledge

Key Requirements

  • Minimum 1 year experience in GMP manufacturing environment
  • Degree in pharmacy, engineering (chemistry/biology), or equivalent
  • Experience with lot dossier review and release activities
  • Fluency in French (oral and written)

Work Rights

Not specified

Tailored Resume

Cover Letter