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Validation Engineer - Ireland

We are currently looking for 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:
Your duties as the CQV Engineer will be varied; however, the key duties and responsibilities are as follows:
1. Oversee the commissioning, qualification, and validation of Autoclaves, CTUs, and Depyro Tunnels.
2. Collaborate with cross-functional teams to ensure compliance with industry standards and regulatory requirements.
3. Utilize Kaye and Vaisala equipment for accurate and efficient validation processes.
4. Provide technical support and troubleshooting for filling lines, lyophilizers, and biotech equipment such as bioreactors.

ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the CQV Engineer, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or engineering discipline.
2. Proven industry experience in commissioning, qualification, and validation within the pharmaceutical sector.
3. A working knowledge and practical experience with Kaye and Vaisala validation equipment.

Key Words: CQV Engineer / Commissioning / Qualification / Validation / Autoclaves / CTUs / Depyro Tunnels / Kaye / Vaisala / Filling Lines / Lyophilizers / Biotech Equipment / Bioreactors

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.

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