QAV Engineer

Ireland is a hive of activity for the Life Sciences Sector at present with global players setting up new/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 one of their existing manufacturing facilities on the West Coast of Ireland. 

Located 30 minutes from an 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.

This position will specifically be accountable for Continuing Validation/Qualification for Utilites and Production Equipment (Upstream / Downstream).

Essential Duties and Responsibilities include, but are not limited to, the following:

• Assists in projects by helping to develop appropriate plans, schedules and other project deliverables as required
• Based on engineering specification, performs validation projects which include authoring protocols, executing validation protocols and writing reports of validation results.
• Reviews Validation protocols and summary reports generated by the Validation team against standard operating procedures and policies.
• Reviews Change Control test plans generated by the Engineering/Automation/Manufacturing teams against standard operating procedures and policies.
• Collaborates with functional departments to resolve issues.
• Excellent communication skills.

Education and Experience:

• Requires a BS/BA in Engineering, Chemistry, or Life Sciences with strong related experience within the field.

To be considered for this position, please apply with a copy of your up to date CV today!

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