CQV Engineer - Pharmaceuticals - 12-Month Contract - Limburg, Netherlands
Our client, a leading partner to pharmaceutical, biotech and nutrition markets, has an exciting opening for a CQV Engineer for their new Capex investment project. As a scientific and technology innovator, this is a superb opportunity to onboard as our client continues to make strides towards a healthier world for all.
Responsibilities:
- Prepare validation documents including URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ, IOQ, OQ, PQ).
- Execution of IQ/OQ and PQ for equipment, systems and utilities.
- Write reports of completed CQV activities
- Stay informed of industry regulatory changes as it applies to equipment / facility validation.
- Support in writing and/or revising procedures applicable to the Engineering activities.
- Support the Engineering group to prepare the validation, requalification and maintenance program.
Required experience:
- Bachelor degree or equivalent in a relevant subject area.
- Flexibility and adaptability, able to perform in an ever-changing environment.
- Demonstrable (3-6 years) experience within a validation role.
- Experience in GMP environment or similar, familiar with GDocP, Data Integrity and ALCOA++
- Strong planning skills and self-motivated, able to work autonomously.
- Business-level fluency in English; other languages are nice to have but not required.
If this role is of interest to you, please apply now! #LI-CB1