STERILISATION VALIDATION ENGINEER required by Career Wise Recruitment for our multinational medical device client in Galway for a fulltime on-site role on an initial 15-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: Bachelors 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.
Please call Laura Gallagher today for further information on or email: Career Wise Recruitment (In Search of Excellence) Established in 1999, Career Wise Recruitment specialises in recruitment of management and technical professionals for the life sciences, ICT, engineering, food and agri sectors.
We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway, Mayo and Dublin.
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Skills: Sterilisation Validation Engineer