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CQV Engineers 12-month Contract
Are you looking to take you career to the next level?
Our Client is a leading global healthcare company with a state-of-the-art pharmaceutical facility in Denmark.
The role, which involves non-shift rotation and requires on-site presence Monday-Friday, offers an opportunity to contribute to a significant new build project. While initially set for 12 months, the contract is likely to extend.
Ideal candidates will possess the following qualifications and experience:
- Proficiency in commissioning, qualification, and validation processes
- Extensive engineering expertise in relevant domains such as process and building services
- Experience validating various products and processes including bio reactors, chromatography kits, and fill and finish equipment
- Demonstrated ability to meet project deadlines
- In-depth familiarity with system startup procedures for new builds
- Competence in protocol generation and execution, including DQ, IQ, OQ, and PQ
- Proven track record in delivering Validation Lifecycle projects, especially on Fast Track Capital Projects
- Skilled in Root Cause Analysis and Problem Solving
- Strong understanding of cGMP requirements and regulatory standards
- Experience conducting FAT and SAT protocols, as well as utilities and process validation
- Familiarity with computer systems validation, Delta V, and change management processes
- Proficient in organizing, reviewing, and reporting daily tasks, along with effective communication with stakeholders across project phases
Requirements:
- Bachelor's degree in science or engineering
- Minimum of 8 years of relevant CQV experience
If you want to learn more... the complete job description and company insights await you upon applying. So why wait? Take the first step towards a transformative career by clicking the "Apply" button below.
This role is being managed by Rebeka Cercizi at Meet, please call me on: +4420 3310 1247
Or email me directly at Rebeka@peoplewithchemistry.com if there is anything you want to discuss.