CQV Engineer
Dublinonsitemid
Posted 2mo ago · via Lever
About this role
Are you an experienced CQV Engineer looking to join a dynamic project team delivering complex pharmaceutical or life sciences projects?
We are seeking a driven and collaborative CQV professional to support commissioning, qualification and validation activities across a range of GMP regulated systems, facilities and equipment. This is an excellent opportunity to work on high impact projects in a fast paced and technically challenging environment.
Key Responsibilities
Execute Commissioning, Qualification and Validation (CQV) activities in line with project schedules and GMP requirements.
Support commissioning, startup and qualification of equipment, utilities and process systems.
Prepare, review and execute validation documentation including protocols, reports, and traceability matrices.…
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
We compare your skills against the role requirements.
2
Level fit
This role is mid-level. We check your trajectory against it.
3
Domain experience
Your work in the role's domain matters more than your years total. We weight recent and direct experience.
4
Recency
A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.
5
Location fit
This role is based in Dublin. We weight your proximity and willingness to relocate.
Score yourself on this role.
Free · no card · written explanation included