Ingénieur (e) Qualité Contrôle Pharmaceutique (Chimie)
Bristol Myers Squibb
Couvet, CH
vor 2 Tg.
source : DirectEmployers Association

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change.

We bring a human touch to every treatment we pioneer. Join us and make a difference. Celgene (a wholly owned subsidiary of Bristol-Myers Squibb) is a global biopharmaceutical company committed to changing the course of human health through bold pursuits in science, life-enhancing therapies, and a promise to always put patients first.

At the core of that mission are the talented individuals who contribute their unique skill sets to help us drive innovation and deliver truly life-changing drugs for our patients.

  • As we continue to pursue that mission, we're looking for talented professionals like you to join our team. In this role, you are responsible for managing QC-Methods validation projects and being A key member of Quality Control Laboratory team In this role, you are responsible for (not limited to) : Data Integrity : + Support analysts on QC Technologies + Support analysts on QC IT software + Review of the logbooks + Support & Train analysts on DI Traning& Issues support : + Support analysts on instrument issues + First contact with supplier and Calibration Team + QC first contact for new instrument implementation + QC Investigation + CCR and deviation / CAPA QC Representative Improvements : + Cost saving and cost avoidance initiatives Your Profile : + BS degree in Chemistry and fluent in both English and French + Minimum 5 years' experience in QC-methods validation within Pharmaceuticals;
  • Minimum 2 years' experience in managing QC-Methods validation projects; + Familiarity with current international regulatory regulations, cGxP requirements and best practices, including USP, Ph.
  • Eur,, JP, 21 CFR part 11, 210 and 211, Annex 11 to EU-GMP + Experience in QC-Instruments purchasing & qualification + Good knowledge of pharmaceutical facilities and laboratory systems;
  • Good communication skills in English with laboratory, technical operations, QA, and outside vendor groups; + Team player : ability to interact effectively with team and customers.
  • Celgene, a Bristol-Myers Squibb Company Around the world, we are passionate about making an impact on the lives of patients with serious diseases.

    Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

    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 with the resources to pursue their goals, both at work and in their personal lives.

    Company : Bristol-Myers Squibb Req Number : R1521544 EN Updated : 2020-06-26 00 : 00 : 00.000 UTC Location : Couvet,Switzerland Bristol Myers Squibb is an equal opportunity employer.

    Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

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