Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
As Quality Excellence Manager, you will have a significant impact on the Quality performance of the Integrated Supply Chain Organisation (ISCO). You will develop and implement programs, processes and tools to establish and drive high quality standards and risk mitigation across ISCO. This will involve working closely with internal stakeholders to prioritize and execute change management. You will also lead projects with a focus on data analysis and digital solutions to support complex problem solving, robust investigations, root cause analysis and effective quality improvement plans to drive continuous Quality improvement at all levels of the organisation.
You will lead the Life Science (LS) Data Integrity program to drive best practice sharing across our manufacturing network and deliver improvement opportunities. You may also provide targeted inspection readiness support ahead of site Regulatory inspections. As Quality Business Partner to the ISCO Head of Engineering and Technology, and their Leadership Team, you will support the development and delivery of the ISCO digital roadmap by providing Quality governance to ensure compliance throughout this digital transformation.
Preferred Locations:
- St. Louis, USA
- Darmstadt, Germany
- Livingston, UK
Who you are:
- Graduate degree (e.g. Pharmacist, Chemist, Microbiologist, Engineer), or equivalent, with extensive knowledge of quality regulations and industry requirements to support a diverse product mix.
- Experience developing Quality Management Systems, solving complex problems and implementing Quality Improvement Programs preferably in the Life Science sector (approximately 5 years as a guide)
- Proven experience in project co-ordination, project plan execution and change management both within a team and in a matrix organisation
- Practical experience of Data Integrity compliance within an Operational environment (approximately 2 years as a guide)
- Strong understanding and experience in the Quality and Regulatory requirements, including validation, of SMART manufacturing and digital systems, for example LIMS and Electronic Batch Records.
- Excellent communication and leadership skills with the ability to work with stakeholders across a matrix structure in a global environment
- Highly motivated, self-driven individual able to work with limited supervision
- Experience of Palantir, Tableau, PowerBI, AERA and other analytics tools beneficial
- The ability to travel, including international travel to global Life Science Manufacturing and Distribution sites
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!
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