Job details
Job type full-time
Full job description
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 healthOur 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 o n challenges that truly matter with people that care for each other, our customers, and their patientsWith 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 termCytiva is proud to work alongside a community of nine fellow danaher life sciences companiesTogether, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
What you’ll do
Lead global programs across cytiva supplier quality with focus on supplier qualification, auditing, capa/rca, change notice management, data analytics, qms, training and standard work
Lead operations management activities within cytiva supplier quality
Identify and develop additional programs to benefit operational excellence, increased rigor and productivity within cytiva supplier quality
Work directly with cross-functional peers to implement or refine input, control and output streams of cross-functional processes
Identify opportunities for continuous improvement of supplier quality process and operations
Who you are
A self-starter who enjoys driving improvement, collaborating with teams and delivering impact
A quality profession with a minimum of 5 years of quality related work experience
Experience in the biotechnology and/or pharmaceutical industry, preferably both.
Knowledge of supplier quality management workstreams including qualification, auditing, change management, capa/rca, qms development and training program development
The desire and ability to travel up to 30%
Ability to develop, communicate and implement a strategy to ensure compliance to cytiva, regulatory and industry requirements
When you join us, you’ll also be joining danaher’s global organization, where 69,000 people wake up every day determined to help our customers winAs an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful danaher business system tools and the stability of a tested organization.
