Validation Engineer

Description

Validation Engineer  Exciting long term contract opportunity available for an experienced validation engineer to work on an expansion project for a world leading pharmaceutical company based in South East England



Key Responsibilities



- Generation, execution and review of life cycle validation documentation for commissioning of facilities, equipment and processes



- To ensure that all documentation is prepared, authorised and completed in a timely manner.



- To ensure that all tasks are carried out in an effective and efficient manner.



- To communicate effectively with others on site and the client associated with the project.



- To maintain an understanding of current international regulatory, ISO, corporate and client requirements relevant to the section.  To ensure compliance with the sections and site procedures.



- To liaise with the various departments involved in the qualification and validation work to ensure the efficient performance of the related tasks.



- To present qualification activities to an auditor



- Comply with GMP requirements and company rules, policies and procedures.



Qualifications/Experience



- Degree



- In-depth knowledge and understanding of cGMP.



- Dynamic, self-motivated, pro-active approach to taking on challenging assignments.



- Creativity, judgement and analytical thinking.



- Ability to work with critical timelines.



- An excellent planner, who can envision short-term milestones which the company must achieve to succeed in the long-term.



- Outstanding communication skills, both written and oral, and the self-confidence to use these skills to convince others to buy-into proposals and plans.



- The drive and maturity to lead combined with the ability to support and interface effectively with projects and motivate cross-functional teams.



 

This is an urgent requirement, please apply immediately for consideration.