Description
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.