Process / Equipment Engineer

Pfizer Com Ec

Ireland
Hybrid
Equipment technical support and troubleshooting
Root cause analysis and capa implementation
Cgmp re-validation and periodic review
Pfizer is seeking a Process/Equipment Engineer for their Bio-Vaccine Suites in Ireland, responsible for providing technical support to ensure equipment reliability and effective manufacturing processes. The role requires significant experience in the biopharmaceutical industry, focusing on equipment troubleshooting, validation, and continuous improvement initiatives

Job Summary

  • Provide process engineering/technical support to support the ongoing requirements of the Bio-Vaccines Suites, ensuring equipment is robust and reliable.
  • Generate and implement documentation for cGMP re-validation and periodic review of systems, equipment and manufacturing processes to ensure equipment remains validated.
  • Use Integrated Manufacturing Excellence (IMEx) and the Digital Operations Centre (DOC) to drive success in Safety, Quality, Supply, Finance and People metrics.

Matching Summary

Match Score: 80

Pfizer is seeking a Process/Equipment Engineer for their Bio-Vaccine Suites in Ireland, responsible for providing technical support to ensure equipment reliability and effective manufacturing processes. The role requires significant experience in the biopharmaceutical industry, focusing on equipment troubleshooting, validation, and continuous improvement initiatives.

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

  • Culture of Right-First Time
  • Partnerships with Operations and Core Engineering
  • Patient centric company values
  • Digital transformation strategy adoption

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