QC specialist

Posted 18 Jan 2023

Aubonne, Vaud - Switzerland

Req Id 258806


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 Specialist (m/f). With the management of the QC analytical support & technology manager, you manage projects related to QC systems (equipment and softwares) needed in the frame of legacy products release and lifecycle management.
You ensure appropriate fitness for purpose of our different QC systems, with the help of our internal and external stakeholders. Thus, you address project management and gather expertises with regards to related requirements (e.g. definition of URS, qualification, cGMP, data integrity, inspection readiness, SOP writing) to maintain automation, innovation and the highest standards of compliance of QC activities.
Being one of the key contact person for this project management expertise, you foster a strong and positive collaboration within the QC analytical & support team (30 people) and beyond, sharing your expertise and scientific background (e.g investigation, troubleshooting).


Who your are :

• Master or Bachelor in Biotechnology/Life Sciences/Chemistry or equivalent with one to five years of relevant experience, respectively

•Languages : French and English (oral and writing)

•Knowledge of qualification/validation activities for equipment, systems

•Experience of project management would be considered as a plus

•Knowledge of laboratory analysis in a GMP environment

•Knowledge of Trackwise, SAP, ManGo softwares, and IT infrastructure knowledge would be considered as a plus

•Theoretical knowledge of the different analytical technologies (HPLC, Biochemistry, Chemistry, Microbiology)

•Ease and appetite to work in a team and in laboratory environment, with international stakeholders and issue related documentation

•Comfortable with delivering timely commitments, being accountable for them to her/his manager and customers, and communicate on their related status


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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