Process Plant Cqv Engineer

Summary : Our client is a biopharmaceutical company in Waterford looking for a Validation Engineer to to support a new project.

The Validation Engineer has a key role in ensuring the on-going validation and compliance of new equipment, systems and processes.

Responsibilities : Executing FAT / SAT / IOQ protocols including generation of protocols and reports.

Designing, executing and reporting on validation studies for equipment, systems and processes.

Ensuring validation studies are managed in conjunction with all required Sanofi standards and legal requirements (Health & Safety, c GMP, construction, environmental etc.) Providing technical interpretation and guidance of current US FDA and EU validation requirements for aseptic processing, lyophilisation, sterilisation and dehydrogenation Ensuring that the validation status of equipment and systems are in compliance with c GMP at all times Maintaining validation documentation through the validation lifecycle Participation in external regulatory inspections Support Site Change Control process Qualifications & Experience : Degree in Science (Chemistry, Micro.

or Pharmacy preferred) or Engineering Chemical / Mech / Elec).

Experience : 3-5 years experience working in a Healthcare manufacturing environment ideally part of which would be in the pharmaceutical sector.

Sees projects / tasks through to completion.

Capable of troubleshooting validation issues associated with projects, process development etc.

Competent technical knowledge of pharmaceutical plants.

Previous validation / product development experience would be highly advantageous for the role.

Knowledge of Process Validation regulations, current process validation and technical