Quality Assurance Validation Consultant

Quality Assurance Validation engineer required to work on a global biotech facility.

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.

They are looking for an individual experienced in executing clean hold protocols and experience writing and approving Deviations/ GMP documents. 

The role will entail activities such as taking Clean hold rinse and swab samples on process equipment and small parts, whilst working closely with manufacturing to ensure the CIP/SIP and holds are achieved and samples are taken.

If you wish to find out more, apply today!!

The candidate must have the rights to work in the location stated in the job advert.

Please note, Quanta Consultancy Services does not sponsor Visa applications.

To view Quanta's privacy policy, please visit our website