Senior Validation Engineer

Collins Mcnicholas Recruitment

Sligo

Senior Validation Engineer. A permanent position has arisen for a Validation Engineer with our client in the Sligo Area. You will work within the QA department of a global pharmaceutical company with responsibility for co-ordination, implementation and participation in the site Validation Program. As Validation Engineer your key responsibilities will include: Validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards. Generation/maintenance of the Validation Master Plans. Generation/maintenance of Project Validation Plans. Generation of validation plans, protocols and final reports to cGMP standard. Review / approval of all protocols and final reports. Management of validation change control process. Adheres to and supports all EHS & E standards, procedures and policies. The ideal candidate will have a proven history of demonstrating a high level of attention to detail, innovative thinking, meeting deadlines, strong work ethic and interpersonal skills. The position has a high level of autonomy and individuals are expected to work on their own initiative with full responsibility for co-ordination and closure of projects assigned in compliance with cGMP procedures & policies and IMB/FDA and company regulations. To apply for this role, all applicants should have obtained a 3rd level qualification in a relevant engineering or scientific discipline. A minimum of 4 years experience in a cGMP regulated environment and a good understanding of regulatory requirements. Excellent remuneration and career prospects aligned to this role. If you fit the above profile, please contact Davin at Collins McNicholas for further details on 071-9142411 or email [email protected] /* */.

3565 days ago