We are currently seeking a CQV Engineer to join a leading pharmaceutical company based in the London area. As the CQV Engineer, you will be responsible for ensuring the commissioning, qualification, and validation of critical equipment.
Key Duties and Responsibilities
* Oversee the commissioning, qualification, and validation of Autoclaves, CTUs, and Depyro Tunnels.
* Collaborate with cross-functional teams to ensure compliance with industry standards and regulatory requirements.
Role Requirements
* A relevant degree in a scientific or engineering discipline.
* Proven industry experience in commissioning, qualification, and validation within the pharmaceutical sector.
* A working knowledge and practical experience with Kaye and Vaisala validation equipment.
To be successful in this role, you should have a strong understanding of industry standards and regulatory requirements. You will be working closely with cross-functional teams to ensure compliance and provide technical support and troubleshooting as needed.
The ideal candidate will have a proven track record of commissioning, qualifying, and validating equipment in a pharmaceutical environment. You should also have a working knowledge of Kaye and Vaisala validation equipment and be able to utilize it effectively.
This is an exciting opportunity for a skilled CQV Engineer to join our team and contribute to the success of our clients.