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: 

INCOMING MATERIAL RELEASE

Raw materials release management :

To perform the release of raw materials according to approved specifications and continuously improve the process and update SOPs related to material release.

To perform the review and approval of materials specifications or update of materials specifications.

To manage deviations, CAPA and CCP related to material release.

Suppliers and materials:

To manage and evaluate Change Notifications related to material release in collaboration with SQM.

CLEAN UTILITIES RELEASE

To manage the release of clean Utilities in collaboration with QC, TDO, QA Engineering and Manufacturing: coordinate activities related to the release (validation of analytical results, manage the deviation related to the release, perform the follow-up of related CCP and trends) and lead the Water/Gas committee.

To collaborate under improvement projects (Pipeline Pilot) for Clean Utilities Release to digitalize the release reports in collaboration with Global functions.

Your profile : 

Chemistry, biology, microbiology or pharmacy master degree with minimum 3 years of experience in Pharmaceutical industry.

Experience in Quality Assurance, Quality Assurance operation or Quality Control is a plus.  

Expertise in cGMP best practices.

Experience in Utilities is a plus.

Good knowledge on laboratory equipment and software (like SAP, Glims, Trackwise…) is a plus

Fluent in French and English

Having a team spirit and being collaborative and curious are essential.  

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!