Ireland is a hive of activity for the Life Sciences Sector at present with global players setting up new and expanding existing manufacturing facilities all over the Country. An exciting opportunity has arisen to work via Quanta on the client’s side for a global Pharmaceutical organisation on a major expansion project based in the picturesque Munster region of Ireland.
Located just 20 minutes from the nearest international airport, the manufacturing site is workable for those wishing to commute to/from Ireland for a contract position. You will be required on site for 5 days per week Monday – Friday working 45 hours.
Essential Duties and Responsibilities for this Quality Assurance Validation role include, but are not limited to, the following:
- Execution, review & approval of SIP/ CIP and continuing validation protocols and closure
- Extensive experience on writing and approving Deviations
- Technical writing experience has written a number of white papers and site reports.
Desirable Experience:
• Experienced Technical writer,
• Experience in Deviation and investigaton writing,
• Experience in Validation specifically CIP/SIP and continuing validation
• Experience in assessment of CIP/SIP issues during study runs and closeout of deviations
• Experience in KAYE validator reporting review beneficial
If this seems like something you would be interested in, apply today!The candidate must have the rights to work in the location stated in the job advert.
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