Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Group revenues in 2022 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). We are guided by our five core values, that shape the way we work, every day: Improve Care, Deliver Results, Grow Together, Own It and Do What’s Right. As a Quality Specialist, you will be in charge of reviewing product documentation, batch review/release, ensuring GMP compliance, and supporting QA Leads in NC / CAPA investigations. Key Responsibilities: • Intermediate product batch review/release • Conduct NC investigations • Support CAPA investigation activities • Complete material dispositions & DAR • Documenting and approving rework activities • GMP Spot checks • Cover for Quality Technicians where required Key requirements Outline the essential competencies and characteristics that candidates must demonstrate to contribute to our diverse, inclusive culture and succeed in the role. These may include: • Good numeracy and literacy skills, capable of performing calculations such as defect percentages. • Capable of using Office spreadsheet packages for data entry and basic calculations • Constructive working attitude and diplomatic approach • Understanding of medical device GMP requirements is highly desirable. Working conditions On-site working 100% at lineside within and outside cleanroom environments. Working shifts: Working 12h nights from 6 pm until 6 am. Monday to Thursday.