We are currently looking for a CQV Engineer to join a leading pharmaceutical consultancy working on projects across the UK on a permanent basis. 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. Utilize Kaye and Vaisala equipment for accurate and efficient validation processes. Provide technical support and troubleshooting for filling lines, lyophilizers, and biotech equipment such as bioreactors. ROLE REQUIREMENTS: 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 is a bonus. Key Words:
CQV Engineer / Commissioning / Qualification / Validation / Autoclaves / CTUs / Depyro Tunnels / Kaye / Vaisala / Filling Lines / Lyophilizers / Biotech Equipment / Bioreactors Seniority Level
Mid-Senior level Employment Type
Full-time Job Function
Engineering, Production, and Manufacturing Industries
Pharmaceutical Manufacturing and Biotechnology Research
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