Process / Equipment Engineer

Pfizer

Ireland
**
Equipment technical support and troubleshooting
Root cause analysis and capa implementation
Cgmp re-validation and periodic review
** Pfizer is seeking a Process/Equipment Engineer to provide technical support for its Bio-Vaccine Suites in Ireland. The ideal candidate will have a background in engineering or science, with 5-8 years of relevant industry experience, particularly in biopharmaceuticals. **

Job Summary

  • Provide process engineering/technical support to support the ongoing requirements of the Bio-Vaccines Suites, ensuring equipment is robust, reliable and all issues are resolved to support the effective and efficient manufacture and disposition of product.
  • Generate and implement documentation for cGMP re-validation and periodic review of systems, equipment and manufacturing processes including Annual Re-Validation Plans and Risk Assessments and IQ/OQ/PQ/QV Protocols and Reports to ensure equipment remains validated.
  • Use Integrated Manufacturing Excellence (IMEx) and the Digital Operations Centre (DOC) to drive success in the Safety, Quality, Supply, Finance and People metrics, identifying process & equipment improvements and safety initiatives.

Matching Summary

Match Score: 75

** Pfizer is seeking a Process/Equipment Engineer to provide technical support for its Bio-Vaccine Suites in Ireland. The ideal candidate will have a background in engineering or science, with 5-8 years of relevant industry experience, particularly in biopharmaceuticals. **

Skills & Requirements

Must-have

  • Equipment technical support and troubleshooting
  • Root cause analysis and CAPA implementation
  • cGMP re-validation and periodic review
  • Regulatory agency inspections
  • Integrated Manufacturing Excellence (IMEx)
  • Digital Operations Centre (DOC)

Nice-to-have

  • Continuous Improvement culture
  • Partnerships with Operations and Core Engineering
  • Proactive equipment reliability concerns
  • Patient-centric company values
  • Diverse and inclusive workforce

Key Requirements

  • 5-8 years' experience in Biopharmaceutical/pharmaceutical
  • Experience with validation/revalidation systems
  • Experience with compliance systems eQMS and QTS
  • Working knowledge of MCS and PI
  • Experience of regulatory inspections
  • Third level Qualification in Science, Engineering or equivalent preferred

Work Rights

Must have authorization to live and work in Ireland

Tailored Resume

Cover Letter