Validation Officer

We are currently looking for a Validation Officer to join a leading pharmaceutical company based in the East Sussex area. As the Validation Officer, you will be responsible for ensuring that all processes, equipment, cleaning methodologies, utilities/facilities, computer systems, and analytical methods are validated.

Your duties as the Validation Officer will be varied however the key duties and responsibilities are as follows:

1. Effectively managing and executing validation projects, providing commissioning, qualification, and validation (CQV) support to new and ongoing projects across the site.

2. Ensuring that validation activities are performed in accordance with company policy and legislative requirements.

3. Composing and reviewing all validation documentation associated with processes, equipment, methods, utilities/facilities, and computer systems.

4. Providing QA input to various other projects on site as required in the maintenance of company Quality Systems with respect to validation and compliance or as deemed necessary by Quality Assurance Management.

To be successful in your application to this exciting role as the Validation Officer we are looking to identify the following on your profile and past history:

1. Relevant degree in an Engineering/Science discipline or equivalent.

2. Proven industry experience in the pharmaceutical sector, preferably with some exposure to validation.

3. A working knowledge and practical experience with Good Manufacturing Practice (GMP).

Key Words:
Validation Officer / CQV / Pharmaceutical / East Sussex/ Quality Assurance / GMP / Validation Projects / Risk Management / Documentation / Compliance / Engineering