Autoclave Validation Lead

Ireland is a hive of activity for the Life Sciences Industry at present with no shortage of major expansion/ new build facilities. We have an exciting opportunity for an Autoclave Validation Lead to join a start-up project for a global pharmaceutical organisation with great longevity of employment possibility.


Located within a commutable distance of one of Ireland’s international airports, this position would suit both local candidates or those wishing to commute from outside of Ireland.

Who are we looking for?

We are looking for an Autoclave Validation Lead with pharmaceutical leadership experience to join this new project for a period of 6 months initially.


Roles & Responsibilities include:

• Ensure CD/PQ readiness
• Execute all CD/PQ protocols (CD runs, air detector runs, GMP air filter SIP runs and empty chamber & full chamber runs)
• Manage Biological Indictors (expiry, incubation etc.)
• Define & Configure Loads (including rack modification if required)
• Prepare Loads for all the cycle runs
• Temperature Map (KAYE equipment – 2 validators to allow for parallel activities)

Experience & Competency:

• Requirement to have successfully undertaken a similar project management role previously
• 5 – 10 years of project management experience in a regulated environment 
• Excellent communication skills (written and oral).
• Excellent collaboration skills and teamwork mind-set.
• Excellent trouble shooting and problem-solving skills, as well as an ability to work through complex problems.

For more information on this project / position, please apply with a copy of your up to date CV today!       



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

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