Posted: 18 June
The role
Senior Process Engineer – Aseptic Manufacturing - Cork - Contract Opportunity
We are supporting a major aseptic manufacturing expansion project and are seeking an experienced Senior Process Engineer to provide technical leadership across sterile filling, isolator technology and process design activities within a live GMP manufacturing environment.
This is a key role within a high-profile brownfield capital project, supporting the development, integration, commissioning and startup of sterile drug product manufacturing operations.
Key Responsibilities:
Lead process engineering activities relating to sterile filling, isolator systems and associated process interfaces.
Support process design, equipment selection, technical specifications and process development activities.
Define process requirements, contamination control strategies, material flows and operational design considerations.
Partner with Engineering, C&Q, Automation, QA, Validation and Operations teams throughout project delivery.
Support commissioning, qualification, startup and troubleshooting activities for aseptic manufacturing systems.
Requirements:
Degree qualified in Chemical, Mechanical, Pharmaceutical, Bioprocess Engineering or a related discipline.
Significant experience within sterile drug product manufacturing, aseptic processing or fill‑finish operations.
Previous aseptic manufacturing experience is essential.
Strong knowledge of isolator technology, sterile process design and contamination control principles.
Experience supporting capital projects within GMP-regulated pharmaceutical or biopharmaceutical environments.
#J-18808-Ljbffr
