Job Description

　　When your part of Thermo Fisher Scientific, you’ll do exciting work, and be part of a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best. With revenues of $40 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.

　　The job:

　　We are a growing Validation Team, based across multiple sites in the UK, looking to bring in a new team leader. The role falls with the Quality function, and works alongside colleagues in other departments, including manufacturing and engineering. In Validation, every day is different, and with varied day-to-day responsibilities, there is always the opportunity to learn something new, develop your skills in this area and meet different people.

　　What will you do?

　　As the Validation Supervisor for the UK sites, you will be managing a team to prepare and execute validation documentation, covering equipment, cleaning and computer system validation, and we also provide support to the process validation team, working closely with them to produce a complete validation package.

　　In this role, you will also manage and mentor the validation team and system owners with the correct approach leading to the successful validation to meet the regulatory standards across multiple sites and processes/equipment.

　　An important part of this position is successful management of senior managers expectations across each site this includes Site Directors, Production Managers and QA managers. This will also include being the point of contact for the UK sites for internal, external, and regulatory audits.

　　Other responsibilities include:

　　· Ensure compliance with safety, health and environment (SHE) legislation.

　　· Ensure annual validation plans area generated, communicated, approved, and reviewed.

　　· Management of External contractors when required.

　　· Connect and communicate with all persons across the business, relaying information on our performance and ongoing projects.

　　Who are we looking for?

　　To fill this role, we are looking for a candidate who has proven experience within a GMP environment, occupying managerial roles in validation, QA or engineering. The role would suit a candidate with validation experience in a medical device ISO13485, biopharmaceutical, consumer health care, microbiology or related industry.

　　Do you excel in planning and time management? Or have problem solving skills you are proud of? Are you a good communicator across the board? Then please come forward as we would like to talk to you. We are looking to engage someone who has the ability to adapt to rapid changes in project priorities and meeting targets.

　　What’s in it for you?

　　• Work within a very close team

　　• Good pension scheme & flexible benefits

　　• An excellent opportunity for career development

　　At Thermo Fisher Scientific, each one of our 120,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.

　　Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.