Process Plant CQV Engineer

Tandem Project Management

  • Waterford
  • Contract
  • Full-time
  • 2 days ago
  • Apply easily
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, cGMP, 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 cGMP 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 transfer industry practices, and experience of interpretation and application of guidelines and regulations.
  • Knowledge of requirements for of GAMP, ISPE Baseline guides.
  • Knowledge of steam and dry heat validation publications such as AAMI/ANSI, PDA and ISO guidelines.
  • Full understanding of relevant quality and compliance regulations
  • Able to execute projects to plan.
  • Ability to use MS Project and SPC packages an advantage
  • Understands KPI's for the site.

Tandem Project Management

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