Project Quality Lead - 12 month FTC

TN United Kingdom; England; On-site; GBP 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a Project Quality Lead to oversee quality assurance for a major capital project. This role offers the chance to lead the creation of a comprehensive Project Quality plan, ensuring all engineering documents meet stringent quality standards. You will collaborate closely with engineers to develop and implement quality strategies that align with regulatory requirements. Join a dynamic team dedicated to making a positive impact in the pharmaceutical and life sciences sectors, where your contributions will help ensure the highest quality standards in manufacturing processes. This opportunity is ideal for those looking to advance their career in a fast-paced and supportive environment.

Benefits

Opportunities for career growth

Diverse and multinational team

Dynamic work environment

Supportive organizational culture

Qualifications

• A scientific degree or equivalent is required.
• Experience in a global regulated environment with quality system knowledge.

Responsibilities

• Lead the creation of the Project Quality plan for a major capital project.
• Review and approve all engineering generated project documents.
• Establish and report on quality metrics for the project.

Skills

Quality System Requirements

Validation Documentation Review

Process Validation

Cleaning Validation

Microsoft Office

Q-Pulse or Electronic QMS

Education

Scientific Degree

Tools

Microsoft Office

Q-Pulse

Job description

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Project Quality Lead - 12 month FTC, Wiltshire

Client:

Location: Wiltshire, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference:

73d16361289b

Job Views:

111

Posted:

10.04.2025

Expiry Date:

25.05.2025

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:

1. 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.
2. The ability to make an impact and shape your career with a company that is passionate about growth.
3. 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?

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

What you’ll do:

1. Lead the creation of the Project Quality plan for a major capital project worth over > £50M.
2. Review & approve all engineering generated project documents including, but not limited to, User Requirement Specifications, Validation Execution Plans, Trace Matrices, Qualification protocols, etc.
3. Work closely with both Purolite process engineers and 3rd party engineers to provide quality input & decisions into the design of the facility.
4. Work closely with both Purolite C&Q engineers and 3rd party C&Q engineers to develop the CQV strategy for project execution.
5. Partner with Site Operations & Engineering organizations to develop and formally document the Process Qualification and Process Validation Strategies.
6. Leverage the existing process’ quality risk assessments to lead the development of new quality risk assessments for the new manufacturing facility.
7. Establish & report out on quality metrics for the project.
8. Measurement of quality metrics & reporting.
9. Ensure the communication between all stakeholders is aligned.
10. Ensure documents are approved on time by Quality management.

What you'll need:

1. A scientific degree, or equivalent.
2. Experience in a global regulated environment with a sound understanding of quality system requirements. (cGMP and ISO9001 advantageous).
3. Experience with equipment, process, and/or cleaning validation.
4. Experience of working in several roles within quality.
5. Software and technical skills, all Microsoft Office applications. (Q-Pulse or other electronic QMS software an advantage).
6. 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.