CQV Engineer

We are currently looking for a CQV Engineer to join a leading Pharmaceutical company based in Denmark. As the CQV Engineer you will be responsible for covering the process from equipment arrival on site over qualification to production.

Your duties as the CQV Engineer will be varied however the key duties and responsibilities are as follows:

1. Carrying out integrity testing

2. Carrying out particle counting

3. Documentation & Testing (SAT)

4. IQ / OQ / PQ

To be successful in your application to this exciting opportunity as the CQV Engineer we are looking to identify the following on your profile and past history:

1. Relevant degree in a Pharmaceutical/Engineering discipline.

2. Proven industry experience in Commissioning, Qualification and Validation.

3. A working knowledge and practical experience with validation of process equipment, black and grey utilities.

Key Words: CQV Engineer / Commissioning, Qualification and Validation / C&Q / Commissioning and Qualification / Validation Engineer / Validation / Validation Consultant / Validation Contractor / GMP / cGMP / Lab Equipment Validation / Laboratory Equipment Validation / Process Equipment Validation / HVAC