QA Validation Specialist

Ireland - Athloneonsitemid

Posted 2 days ago · via Workday

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About this role

This is what you will do: The QA Validation Specialist performs review and approval activities to support validation activities in Alexion ARDU cGMP commercial and clinical requirements for the Alexion Manufacturing Facility. The responsibilities will include performing review and approval of validation documents such as policies, master plans, procedures, specifications, investigations, protocols and reports. You will be responsible for: Maintenance of a strong Quality culture throughout the project through operational activities. Provide QA support for risk based verification activities in the capacity of Quality Assurance Subject Matter Expert. Review and approval equipment/utilities verification documentation from design to post execution.…

Read the full description on BP01 Alexion Pharmaceuticals Inc's site →

What we'd score you on

reqspace match rubric

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Skills match

For this role: vault, linear

Level fit

This role is mid-level. We check your trajectory against it.

Domain experience

Your work in the role's domain matters more than your years total. We weight recent and direct experience.

Recency

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Location fit

This role is based in Ireland - Athlone. We weight your proximity and willingness to relocate.

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Skills in this role

Pulled from the job description. These are the keywords we'll weight when scoring your fit.

vaultlinear

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