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Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry 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. Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Summary of purpose of role. Responsible for developing, implementing, and optimizing production processes to ensure efficient, safe, and cost-effective operations. Minimize equipment downtime and enhance productivity by leading continuous improvement initiatives driven by performance data and root cause analysis. • Work with maintenance and production associates to resolve manufacturing and quality problems related to methods, processes, tooling, equipment, and product design., • Use root cause analysis to solve complex manufacturing and quality issues, • Develop manufacturing and/or testing processes with focus on safety, quality, and repeatability for New Product Introduction/Sustainment projects., • Follow best practices around Process Development (PD), Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) with a goal to develop Safe and Quality Processes, • Create standard operating procedures (SOP) or work instructions and provide training and guidance to others, • Hold formal qualifications (Bachelors Degree) in an Engineering discipline or time served in a Process/Manufacturing role., • Strong Process Engineering background and a detailed understanding of process validation requirements in a manufacturing environment., • Works well under time-bound pressure as part of a team, and independently., • Strong documentation skills (work instructions, manufacturing plans etc) with a keen eye for detail, • Self-motivated and committed to upholding high standards of Safety, Quality and Delivery. For more information, visit

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. The Regulatory Affairs Specialist for Cytiva is responsible for supporting regulatory compliance of Medical Devices placed on the market in EMEA. This position is part of Medical Regulatory Affairs located in Portsmouth, UK and will be on-site. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: • Compile all aspects of Technical Documentation for product certification under Regulation (EU) 2017/745 for Medical Devices., • Submit Technical Documentation to Notified Bodies for review and approval., • Support RA related QMS documentation, Complaints Assessment, Vigilance Reports and Change Controls., • Support medical device Regulatory Intelligence process and customer requests., • Provide support as required for UK Responsible Person with regard to the requirements set out in the UK MDR 2002 relating to medical devices., • You have a Life Sciences degree or equivalent., • You have at least 2-3 years experience in a healthcare / life sciences industry in a regulatory or technical field., • Working knowledge of Medical Device regulations (EU MDR, MDCG guidelines, other EMEA), ISO 13485 and ISO 14971., • Experience with Quality Management System documentation., • Ability to communicate effectively across all departments and functions, • Good attention to detail., • Have excellent English oral and written communication. For more information, visit

Proven experience in product development, engineering design, or innovation within a manufacturing environment. Innovation & Development Engineer. Conduct research and analysis to identify market trends, customer needs, and regulatory changes influencing product innovation.

You’ll inherit and lead a team of 8 (product designers, content designer, visual designers, and user research), empowering them to shape products, marketing, communications and services used by millions of UK households. We’re looking for a Head of Experience Design to lead our multidisciplinary

Product Catalog & Research Analyst. Product Catalog & Research Analyst at Uvation. Product Research of North America/Global Catalogue.