Beschreibung
Title: CQV Engineer
Rate: Negotiable
Location: Frankfurt, Germany
Type: Contract (12 Months)
A Fantastic new role has just opened up at one of our leading Hessen based clients offering the successful candidate the opportunity to join a hard-working team working on exciting projects in the pharmaceutical sector.
The proposed start date is ASAP - We need YOU
Responsibilities include:
- Full qualification and validation of on-site utilities and equipment in a pharmaceutical manufacturing environment (inc. autoclaves)
- Working with the Director to review/update the Validation Master Plan.
- Writing and executing of FAT, SAT, DQ, IQ, OQ protocols of equipment and utilities.
- Analysis and validation of third-party protocols and processes. This includes performing gap analysis and risk assessments of documentation procedures.
- Prepare protocols, progress and final reports on all validation project.
Requirements
- A bachelor's degree in science, pharmacy, or engineering field is preferred.
- A wide range of qualification experience across different equipment and utility types.
- An experience and the ability to carry out full IQ, DQ, CQ, OQ, and PQ.
- Basic German skills
If you are interested by this role then get in touch with me!
(see below)