At a Glance
- Tasks: Lead quality planning for a major £50M project and review engineering documents.
- Company: Join Purolite, a global leader in resin-based technology, making the world cleaner and safer.
- Benefits: Impactful work, diverse team, and opportunities for career growth in a dynamic environment.
- Other info: Collaborative culture with a flat management structure encouraging innovative ideas.
- Why this job: Shape your career while tackling meaningful challenges in the pharmaceutical and life sciences sectors.
- Qualifications: Scientific degree and experience in regulated environments; quality system knowledge is a plus.
The predicted salary is between 50000 - 60000 £ per year.
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.
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
How You’ll Make an Impact:
- 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
Qualifications:
- 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
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
Ecolab’s Commitment to Diversity, Equity and Inclusion (DE&I)
Ecolab’s commitment to diversity, equity and inclusion (DE&I) reflects our longstanding value of working together to integrate diverse perspectives to challenge ourselves, reach our goals and do what’s right.
Project Quality Lead - 9 month FTC in Llantrisant employer: Dormont Manufacturing Co
At Purolite, an Ecolab company, we pride ourselves on being a world leader in resin-based separation and purification technology, offering a dynamic and entrepreneurial workplace at our cutting-edge manufacturing site in Llantrisant, Wales. Our commitment to employee growth is evident through our diverse, multinational team and the opportunity to tackle meaningful challenges that contribute to a cleaner, safer, and healthier world. Join us to make a significant impact while enjoying a supportive culture that values innovation and collaboration.
StudySmarter Expert Advice🤫
We think this is how you could land Project Quality Lead - 9 month FTC in Llantrisant
✨Get Familiar with Temporary Roles in Pharma
Temporary positions in the pharmaceutical industry often arise during specific periods, like product launches or seasonal hiring sprints. Keep an eye on timelines and be proactive in reaching out to companies, especially around these busy times!
✨Join Pharma Networking Events
Participate in local and virtual pharmaceutical networking events or job fairs. This is a fantastic way to get in front of hiring managers and learn more about temporary opportunities directly from those in the know.
✨Leverage Your University Career Services
If you’re a student or recent grad, tap into your university’s career services which often have specific connections to pharma companies looking to fill temporary roles. They might even have exclusive internship programmes that lead to temp jobs!
✨Be Visible Online and Offline
Utilise platforms like LinkedIn to share your interests in temporary roles and connect with industry professionals. Plus, consider writing about relevant pharmaceutical topics to showcase your knowledge and enthusiasm—this can help you stand out to hiring companies like Dormont Manufacturing Co.
We think you need these skills to ace Project Quality Lead - 9 month FTC in Llantrisant
Some tips for your application 🫡
Highlight Your Relevant Experience:In the pharmaceutical industry, it's crucial to showcase any relevant experience you have, whether it's internships, lab work, or coursework. Let’s emphasise your familiarity with drug development processes and any hands-on experience you've had with lab equipment or clinical trials in your CV.
Mention Certifications and Training:If you’ve got any certifications relevant to pharmaceuticals, like Good Clinical Practice (GCP) or a certification in pharmacovigilance, make sure to include them. These show your commitment to the field and can make a positive impact on your application for a temporary role at Dormont Manufacturing Co.
Show Your Flexibility and Availability:Temporary positions often require immediate availability and flexibility in working hours. In your cover letter, make it clear when you can start and your ability to adapt to changing schedules, as this is key to a successful application.
Express Your Learning Goals:Since this is a temporary role, we suggest discussing what you hope to learn or gain from the experience at Dormont Manufacturing Co. This not only shows your eagerness but also helps employers see you as someone who’s ready to make the most out of the opportunity.
How to prepare for a job interview at Dormont Manufacturing Co
✨Know Your Regulations
In the pharmaceutical industry, it’s crucial to understand key regulations like GMP (Good Manufacturing Practices) or GCP (Good Clinical Practices). Brush up on these standards and be ready to discuss how they influence your work approach during your interview with Dormont Manufacturing Co.
✨Emphasise Adaptability
Since this is a temporary role, show that you're ready to hit the ground running. Share examples from your past experiences that demonstrate your ability to adapt quickly to new environments or changes, especially in a fast-paced setting like pharmaceuticals.
✨Highlight Relevant Skills and Tools
Whether it’s laboratory techniques or software like LabWare or SAS, make sure you can confidently talk about your technical skills. If you have experience with any specific tools used in previous roles, relate that directly to how it can help Dormont Manufacturing Co achieve its goals.
✨Prepare for Technical Questions
Be ready for technical questions related to drug development processes or quality assurance. We should expect scenarios where you might have to troubleshoot a problem or suggest improvements on a project—this shows your problem-solving capability in a temporary role.
