Bristol-Myers Squibb is a global
Biopharma company committed to a single mission : to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.
Join us and make a difference.We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development.
Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.
In this role, you are responsible to perform all type of analytical testing that is required for release of packaging materials and all the environmental sampling.
The role includes the documentation management for the QC Laboratory, the sample management and the management
of the consumable (Reagent & others) by purchasing, receptioning and providing the Couvet
Laboratory in time with materials. The management of the standards for the analytical testing is under your responsibility.
As a QC team member, you support all activities to continuously maintain the GMP status of the QC Laboratory.
The main tasks include (but are not limited to) :
You have :
Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.
Working with Us
By fostering a culture of inclusion, we empower this 21st century workforce to achieve our company's mission of helping patients to prevail over serious diseases.
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A clear purpose. An inclusive culture. The chance to work at the top of your field. These are a few of the reasons Bristol-Myers Squibb is the right choice for your next career move.
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