CQV Engineer

We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Athlone. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. The CQV Engineer will be responsible for life cycle qualification documentation. This specific role is for Process Equipment in a solid dosage environment. They will work with the Equipment Project Lead to ensure the system is commissioned and qualified as expected. The role is client-side, and will be accountable for c...

Location: Roscommon,

Validation Engineer Intermediate

Validation Engineer Intermediate Onsite RK5634 Contract 12 months Dublin We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Key Responsibilities: Provide expert technical validation support to meet site objectives, comprising of the full validation lifecycles process from initial design through qualification to validation maintenance (eg. Periodic review) Coor...

Location: Dublin,

MSAT Validation Engineer

We’re currently recruiting for an exciting opportunity with an award-winning biopharmaceutical organization based in Dundalk. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Key Responsibilities: Lead/Execute/Participate in Equipment and System Validation Lifecycle processes, Qualification (IQ/OQ/PQ), Revalidation, Requalification and Equipment Periodic Reviews, for Equipment and Systems. Coordinate with and guide other departments or outside contractors/vendors to co...

Location: Cork,