C&Q / Validation Manager - South Ireland

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My Client, a Pharmaceutical Manufacturer in the Cork area is currently looking for a Validation Manager to join the company on a rolling contract basis.The site is currently undergoing an expansion and as such you would have a strong technical input on the Project.Duties:

'€¢Leading a team of 10 Engineers to develop and implement a CQV programme'€¢Providing technical direction on projects'€¢Develop project URS's'€¢Implement and manage the Commissioning, Qualification & Validation documentation process

Experience Required:

'€¢Implementation and execution of equipment qualification (IQ, OQ, PQ) will also be a responsibility'€¢Previous managerial experience, specifically in a Validation or C&Q role'€¢Performing Validation studies

'€¢Thermal Sterilisation'€¢Autoclave Validation'€¢SIP Validation'€¢Current/recent experience in a GMP Pharmaceutical/Biotech environment

If this role is of interest and you fit the specifications listed above then do not hesitate in getting in touch. My Client is realistically looking at interviews from next week onwards but is collecting CVs this week to review. Ideally they would require someone in the position by mid-February but may be flexible for the right person too.  CIP / PHARMACEUTICAL / BIO / VALIDATION / C&Q / GMP / URS / CQV / AUTOCLAVE