Working with an international, award winning CDMO based near the coast of Ireland, I am supporting the senior operations team appoint several validation / qualification experts on an interim basis, in order to oversee a critical expansion project.
With the project underway and equipment procured, qualification processes are expected to begin in May and June and will last approximately three to four months.
Bringing in significant experience in pharmaceutical GMP settings, you will support a small permanent team with key qualification activities. Given, the size of the team, you will most certainly be hands on in all aspects and also have the experience to build key stakeholder relationships quickly and effectively.
The role is expected to be on site full time and will need someone based within a commutable area. There is a competitive hourly rate on offer.
Key experience:
* Validation and/or qualification engineering professional with extensive GMP experience in a pharmaceutical setting
* Stakeholder management skills
* To be hands on and drive processes forwards
* Available from end of May/early June
* To be based on site full time
To learn more about this opportunity, please contact Mark Bux-Ryan.
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