Validation Engineer – CSV/IT

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Job PIN:
SBR48081
Job Status:
permanent
Location:
Midlands, West, South
Job Title:
Validation Engineer – CSV/IT
Job Type:
Scientific
Salary:
€50,000 - €55,000
Job Description

 

Validation Engineer – CSV/IT  

This company is one of the largest pharmaceutical companies in the world with operations in Munster. Due to expansion, an exciting opportunity has arisen in their manufacturing facility in the Munster.

Responsibilities of the role will include: 

  • Co-ordination, implementation and active participation in the site validation programme for  computer systems and cleaning.
  • Provide input into all project phases i.e. from design through to the commissioning and qualification execution phases of the project.
  • Develop validation documentation as required (e.g. specifications, plans, protocols, procedures etc.).
  • Review and approve documents prepared by the validation team, other departments and contractor organisations (e.g. commissioning test plans, impact assessments, change controls).
  • Execute qualification protocols as required and prepare reports of executed protocols.
  • Resolve and assist in the closure of deviation initiated during qualification execution.
  • Initiate and implement change control activities in accordance with site procedures.
  • Co-ordinate re-validation activities and generate SOP’s / other documentation as applicable.
  • Conduct training in validation methodologies and related procedures as required.
  • Present validation systems at internal and external audits and support quality assurance programmes.
  • Conduct validation activities in compliance with US and EU regulations, global procedures and EHS requirements.

Candidates for the role should have the following education, skills and experience:

  • Relevant 3rd Level Qualification in science or engineering.
  • A minimum of 3 years IT validation experience in an established QA function preferably in the healthcare industry.
  • Strong knowledge of CSV/GAMP,21CFR Part 11,Project Life Cycle and cGMP Regulations.
  • Cleaning validation experience would be an advantage.
  • Strong statistical skills and process capability are required along with excellent interpersonal, communication, facilitation and team working skills.

For immediate consideration for this role please apply online or contact:

Shane Browne - (01) 632 1865

HRM Science Selection Team

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