Biopharma Process Engineer: Equipment, Validation & CI

Pfizer

South Dublin

Hybride

EUR 70 000 - 95 000

Plein temps

Il y a 2 jours
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Résumé du poste

Pfizer in Ireland is seeking an Equipment/Process Engineer for the Bio-Vaccine Suites to provide process engineering support, ensure robust and reliable equipment, and resolve issues to sustain manufacturing efficiency. You will lead root cause investigations, CAPA, and participate in validation and periodic reviews with cGMP compliance, supporting audits and continuous improvement through IMEx and DOC.

Hybrid work in Ireland, 3-5 years Biopharmaceutical experience preferred; third level

Qualifications

  • Third level qualification in Science or Engineering.
  • 3-5 years’ experience in the Biopharmaceutical/pharmaceutical industry.
  • Experience with validation/revalidation is advantageous.

Responsabilités

  • Provide routine equipment technical support and troubleshooting for manufacturing issues.
  • Lead root cause investigations and CAPA implementation.
  • Support validation activities and periodic review programs for equipment and processes (IQ/OQ/PQ/QV).
  • Drive continuous improvement and participate in Capital Project teams as SME for end-user requirements.

Connaissances

Root cause analysis
Troubleshooting
CAPA
Communication

Formation

Science/Engineering degree

Outils

eQMS
QTS
MCS
PI

Description du poste

Pfizer in Ireland is seeking an Equipment/Process Engineer for the Bio-Vaccine Suites to provide process engineering support, ensure robust and reliable equipment, and resolve issues to sustain manufacturing efficiency. You will lead root cause investigations, CAPA, and participate in validation and periodic reviews with cGMP compliance, supporting audits and continuous improvement through IMEx and DOC.

Hybrid work in Ireland, 3-5 years Biopharmaceutical experience preferred; third level

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