Senior Validation Engineer – Pharma

Andrew Bolton at CK Engineers is currently recruiting for a Senior Validation Engineer to join a leading Pharmaceutical Manufacturer at their site in Suffolk on a full time, permanent basis. This role is based commutable from Suffolk, Cambridgeshire & Essex regions.

As a Senior Validation Engineer, you will be responsible for:
– Leading validation & qualification (IQ/OQ/PQ) activities across the manufacturing site including coldchain projects, large-scale API manufacturing plant, production equipment & automated control systems as well as processes.
– Review, prepare, execute & report validation documentation (Incl. IQ/OQ/PQ, ASTM, FDA, MHRA & cGMP).
– Support change projects through completion of revalidation activities.
– Participate in HAZOP & Quality reviews.
– Carrying out temperature mapping of facilities, systems & equipment.
– Advising on-site teams on any validation or related issues & activities.

As a Senior Validation Engineer, you will have the following qualifications, skill sets & experience:
– A qualification in an Engineering or relevant discipline (or equivalent) or equivalent experience.
– Demonstrated experience in a Validation Engineer / Validation Officer function including application of IQ/OQ/PQ principals.
– Experience gained within a Pharmaceutical Manufacturing or related environment.

This is an excellent opportunity for a Senior Validation Engineer to join a leading Pharmaceutical Manufacturer, who in return offers a salary of £33,600 – £44,280depending on experience, coupled with excellent benefits.

CK Engineers is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.