Purolite, an Ecolab company, the world leader in resin-based separation, purification and extraction technology, is seeking a Quality Validation Specialist at our state-of-the-art manufacturing site in Llantrisant, Wales!

At Purolite, we manufacture products which help our customers around the globe, mainly in pharmaceutical and life science sectors, with technology which are critical to safe manufacture of their products. It’s an exciting business which helps make the world cleaner, safer and healthier.

Purolite is seeking a Quality Validation Specialist who will work within the UK quality team and contribute to the efficient support of the review of the validation documentation for a new project build.

What’s in it For You:

• The opportunity to take on some of the world’s most meaningful challenges, helping customers achieve clean water, safe food, abundant energy and healthy environments
• The ability to make an impact and shape your career with a company that is passionate about growth
• The support of an organization that believes it is vital to include and engage diverse people, perspectives and ideas to achieve our best

Why choose Purolite?

• A world-leading international organization, benefitting from a diverse, multinational team
• A fast-paced, dynamic, and rapidly growing environment
• Manufacture of high-quality technical products, developed hand-in-hand with leading minds in the industry
• Entrepreneurial workplace culture with a flat management structure, encouraging new approaches and ideas

What you’ll do:

• Support the establishment of the Quality plan for the project.
• Conduct a review of the validation document.
  • URS, FRS, TRS FAT/SAT, IQ, OQ, and PQ for manufacturing processes.
  • Verify that all quality key attributes are correctly managed and tested.
  • Ensure that a green light is coming from quality to move to the next step.
  • Review all validation reports.
• Ensure all modifications are captured and managed correctly.
• Ensure the communication between all stakeholders is aligned.
• Ensure documents are approved on time by Quality management.

What you'll need:

• A scientific degree, or equivalent.
• Experience in a global regulated environment with a sound understanding of quality system requirements. (cGMP and ISO9001 advantageous)
• Experience with equipment, process, and/or cleaning validation.
• Experience of working in several roles within quality
• Software and technical skills, all Microsoft Office applications. (Q-Pulse or other electronic QMS software an advantage)
• Confident and flexible working attitude; work within an environment that has quickly changing priorities and deadlines to satisfy validation requirements.