JOB DESCRIPTION
Purolite, an Ecolab company, the world leader in resin-based separation, purification and extraction technology, is seeking a Project Quality Lead 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 Project Quality Lead 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:
Lead the creation of the Project Quality plan for a major capital project worth over > £50M.
Review & approve all engineering generated project documents including, but not limited to, User Requirement Specifications, Validation Execution Plans, Trace Matrices, Qualification protocols, etc.
Work closely with both Purolite process engineers and 3rd party engineers to provide quality input & decisions into the design of the facility
Work closely with both Purolite C&Q engineers and 3rd party C&Q engineers to develop the CQV strategy for project execution.
Partner with Site Operations & Engineering organizations to develop and formally document the Process Qualification and Process Validation Strategies
Leverage the existing process’ quality risk assessments to lead the development of new quality risk assessments for the new manufacturing facility
Establish & report out on quality metrics for the project
Measurement of quality metrics & reporting
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.
Our Commitment to Diversity and Inclusion
Ecolab is committed to fair and equal treatment of associates and applicants and furthering the principles of Equal Opportunity to Employment. Our goal is to fully utilize minority, female, and disabled individuals at all levels of the workforce. We will recruit, hire, promote, transfer and provide opportunities for advancement based on individual qualifications and job performance. In all matters affecting employment, compensation, benefits, working conditions, and opportunities for advancement, Ecolab will not discriminate against any associate or applicant for employment because of race, religion, color, creed, national origin, citizenship status, sex, sexual orientation, gender identity and expressions, genetic information, marital status, age, or disability.
