QC Planner (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: 

An exciting new opportunity has arisen to join our production site in Aubonne as QC Planner (m/f/d). With the management of the QC analytical support & technology manager and QC senior associate director, you manage the analytical Planning Strategy and execution for Drug Substance and Drug Product manufactured at Aubonne Site, and you drive accordingly the QC projects needed in the frame of legacy products release and lifecycle management.
You ensure appropriate fitness for purpose of the different QC projects (planning, LCM, compliance, efficiency, business continuity, reorganization), ensuring appropriate understanding and respect of stakeholders needs.
Being one of the key contact person for this analytical planning and project management expertise, you foster a strong and positive collaboration within the QC and beyond, sharing your expertise and ensuring accountability of the different stakeholders. You ensure reliability of QC commitment and liaise with SNO, Site Planning, Production teams, maintaining and communicating the QC testing schedule.

Who your are:

• BSc in Management/Industrial Engineering or related discipline with minimum of 3 years hands on experience in a GMP Environment, preferred Quality Control or Manufacturing.
• Experience of planning analytical activities and use of related planning tools
• Experience of project management in Quality Control, and in Pharmaceutical Production
• Proven experience of operational excellence project, and of validation processes in a GMP environment
• Demonstrated leadership skills and outstanding interpersonal, communication and motivation skills.
• Excellent written and verbal communication skills and experience of working with teams and influencing decisions.
• Have experience leading cross-functional teams and knowledge of project management/operational excellence tools.
• Theoretical knowledge of the different analytical technologies (UPLC, Biochemistry, Chemistry, Microbiology)
• Languages : French and English (oral and writing)

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!