A Sterilisation Validation Engineer is required by CareerWise Recruitment for our multinational medical device client in Galway for a fulltime on-site role on an initial 17-month contract.
The Sterilisation Validation Engineer will support sterility assurance activities for new products and change control, developing strong partnering relationships with these groups, at both manufacturing and design sites.
The Role
Participate in root cause investigations and continuous improvement in day-to-day activity, initiating appropriate corrective actions and following through to implementation.
Support cross functional teams in design protocols to ensure that new products/ product changes are adequately evaluated/tested to guarantee compliance to all regulatory standards.
Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
Requirements
Bachelor’s Degree (Level 8) in a relevant Science Engineering or other technical discipline.
1-2+ years’ experience in a GMP environment.
Experience in Sterility Assurance or Microbiology ( Endotoxin, Bioburden etc) would be of interest.
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