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. Your health wellbeing are important to us and together we will not compromise on safety in the workplace or the environment.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.

• Leading continuous improvement initiatives to ensure Cytiva’s compliance processes are operationalized, fit for purpose and easy to apply.
• Working with the Commercial Compliance team to improve the internal standard work across all key areas (Customer Interactions, Channel Partners, KYC, KYS, Audit & Monitoring, Training, Agreement Templates) to drive consistent and effective execution globally
• Collaborating closely with the COLR team to align compliance initiatives with legal priorities and with the Operations (COO) teams to identify other areas of improvement to mitigate risk effectively.
• Collaborating with OPCO and Regional Compliance directors to improve and deliver effective commercial compliance training through the GTM and NEO training programs
• Executing compliance projects and countermeasures to successful completion and sustainment by applying strong project management and DBS principles and tools