QC Validation Analyst - 12 month FTC

• 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.

• 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.

• 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 validation 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 validation reports in a timely manner.
• To collate and trend data associated to the validation procedures.

• 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 have experience performing tasks associated to method validation.
• 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.

Ecolab