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.
What you'll do:
Act as Quality SME and manage daily deployment and priorities of the Quality Technician/Engineering team to support customer and manufacturing complaint investigations and improvement actions
Author and review technical reports providing feedback and coaching on best practice, enabling associate development
Provide skills and career path development and guidance to team members
Work cross functionally with key stakeholder departments such as operations, engineering, supply chain and maintenance to deliver projects, resolve issues and deliver compliant outcomes
Deploy and embed new procedures and policies ensuring compliance to requirements
Maintenance, reporting and escalation as necessary of departmental and supporting site KPIs
Support other functions within the department as necessary
Who you are:
Degree or equivalent in Scientific, Engineering or Quality discipline (or equivalent working experience)
At least 5 years experience of managing teams of professionals working in a manufacturing based quality environment
At least 5 years experience in a relevant Quality Engineering role (e.g. pharma, med device, automotive, aerospace), where compliance in a fast paced business is critical
At least an advanced level of operating within an ISO9001 environment and knowledge of ISO13485, 21CFR820, GxP and Pharma regulations would be advantageous
Experience of writing problem statements and executing best practice in CAPA
Demonstrative experience of using ISO14971 risk management principles and application
Experienced in deploying strategy and setting and delivering objectives within a team
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
