Validation Engineer

Our leading global Pharmaceutical client is currently looking for a Validation Engineer, for 3-6 months, to support the completion of a large sterile project. This individual will join a team of Validation Engineers to perform a number of duties in order for the project to finish on time and in budget.

Responsibilities
Writing and/or executing IQ/OQ/PQ protocols & validation documentation
Ensuring all documentation is prepared, authorised and completed in a timely manner.
Warranting all tasks are carried out efficiently and effectively.
Complying with GMP requirements and company rules, policies and procedures.

Requirements
A background in sterile manufacturing, installing new filling lines and working with Vial or syringe lines.
Working knowledge in Sterilisation Tunnels, VHP, Hydrogen Peroxide Methods, Autoclaves, Disinfectants, Inspection Machinery.
Experience with working towards EMEA regulations.
A strong background in writing and execution of validation documentation.
An excellent track record of Validation Engineering roles throughout career.
Good people/communication skills.

If you are looking to join this international dominating company please apply today with an email highlighting your key skills and relevant experience aligned to this opportunity.