BE PART OF SOMETHING ALTOGETHER LIFE-CHANGING!

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
Responsible for providing quality assurance leadership and support to the Process Design & Validation Services (PDVS) business unit,. The PDVS team provides laboratory services to our BioPharma customers, as well as supporting internal R&D and manufacturing projects.
This is an on-site position located at the Harbourgate site in Portsmouth, UK.

• Take responsibility for BU QMS documentation and processes to ensure compliance with the Corporate ISO9001 QMS, industry and regulatory requirements.
• Manage deviation and CAPA process. Ensure deviations are correctly captured, investigated, and trended, and that appropriate CAPA activities are initiated and completed within agreed timelines. Monitor effectiveness of CAPA.
• Host customer, third party and internal audits.
• Support the business in delivering against Quality KPIs.
• Support the Global PDVS Quality Leader on global Quality related initiatives.