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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: In the context of a multinational pharmaceutical company undergoing Site development, a new building for aseptic filling is currently under validation to support the production of parenteral products.
As part of the Manufacturing Science and Technology Fill and Finish department, you will participate in the validation of manufacturing processes or cleaning processes related to products transferred to the new production lines.
You will be a member of the validation team which deals mainly with process changes and monitoring of current processes (through establishing Process Control Strategy (PCS) and Continued Process Verification).
You will also be responsible for the preparation, execution and reporting of documentation related to process and cleaning validation including preliminary risk evaluation.
This project function will give you the opportunity to perform the changes from start to end.
This role is an opportunity for large collaboration in several departments and multiple sites of the Company Network.
Who you are: Education level: Pharmacist, CTF, Biotechnologist 1-3 years of experience in the validation topic Experience working with GMP Validation process and statistical knowledge; QbD approach is a plus Fluent in spoken and written English Product Tech Transfer knowledge Experience in Aseptic filling is a plus Regulatory knowledge is a plus 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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