Purolite, an Ecolab company, the world leader in resin-based separation, purification and extraction technology, is seeking a Quality Control Stability Analyst 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 Control Stability Analyst who will work within the Quality Control department contributing to the efficient day-to-day operation within the lab, supporting the Llantrisant manufacturing site.  

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:

• All QC Analyst level 2 responsibilities.
• To perform routine analysis of finished products in an efficient and effective manner in full compliance with relevant documented procedures to support the stability program.
• To be able to plan and prioritise own day to day workload. 
• To assist in preparation of technical documentation within the department, as required. 
• To assist in training of others, as required. 
• To ensure that all work carried out complies with departmental procedures.
• To assist in the performance of project work within the team, as required. 
• To review analytical and laboratory data within the team for accuracy, completeness, and compliance with documented procedures. 
• Generation of stability reports in a timely manner.

What you'll need:

• A scientific degree in the field Chemistry or related subject.
• Experience in using HPLC, GC and UV/Vis analytical techniques.
• IT literate with a good level of experience using Microsoft Office, particularly Excel.
• Excellent communication skills are required, with the ability to liaise effectively with colleagues at all levels.
• Be highly self-motivated and have the ability to work with the minimum supervision, whilst at the same time being a strong team player.
• Experience working in an ISO: 9001, FDA, MHRA regulated laboratory.
• Understanding the ICH guidelines and having experience performing tasks associated to the stability program.
• Knowledge or experience of downstream process chromatographic material would be beneficial.
• Experience of packing chromatographic material into columns would be beneficial.
• Experience of using FPLC systems would be beneficial.