Expert management risks and changes - m/f/d

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.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your Role:

As a member of the Quality System & Compliance group, your role involves acting as the process owner for change control and risk quality processes. You'll be responsible for ensuring that these processes are designed, implemented, and maintained in accordance with regulations and industry standards. Additionally, you'll oversee the implementation of associated training to ensure effective execution of these systems at the site level. Integration of these systems into all aspects of site operations falls under your purview, as does conducting regular monitoring and analysis of their performance. Furthermore, you'll provide support during inspections and audits in your capacity as process owner.

As member of the Quality System and Compliance group, you will also: support the continuous improvement of the site Quality Systems and contribute to ensure state of compliance of other quality systems act as Key User and administrator of computerized Quality management systems (back-up) implement new regulatory or Quality standards and/or quality systems requirements support continuous improvement in digital transformation and digital roadmap support Quality and Performance metrics

Projects:

Automatization of routine tasks (with tools like Power Apps, Power Automate) and processus

Continuous improvement of area under your responsibilities

Contribute to site digitalization roadmap and future eQMS

Your Profile:

University degree (min Bachelor) in scientific education.

5+ years of experience in the pharmaceutical industry, including Quality Systems management and manufacturing processes.

Experience in change control/risk management.

Experience in Health Authorities Inspections is a plus.

Digital mindset and knowledge, promoting continuous improvement and innovation.

Ability to drive collaborations with cross-functional teams, demonstrating good project management skills.

Personal accountability for results and integrity, with a solution-based thinking and risk-based approach.

Strong organizational skills, including time management and planning, with fluency in French and English.

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!