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bristol-myers squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.one shared journey is moving us forward at bristol-myers squibb. .....
job descriptionwhen you’re part of the team at thermo fisher scientific, you’ll do important work, like helping customers in finding cures for Cancer, protecting the environment or making sure our Food is safe. your work will have real-world .....
description about baxter baxter provides a broad portfolio of essential renal and Hospital products, including home, acute and in-center dialysis; sterile iv solutions; infusion systems and devices; parenteral Nutrition; Surgery products and .....
global quality, Clinical trials & safety is responsible for Auditing all processes related to Clinical research and Pharmacovigilance activities, to assess Compliance with relevant regulations and applicable policies and procedures. this .....
global quality, Clinical trials & safety (gq-ct&s) is responsible for the quality governance and Auditing of Clinical trials and safety. gq ct&s defines the Clinical Quality management systems (qms) enabling strategies and technologies .....
    a fantastic opportunity is available for a regional audit Compliance manager to join our safety, quality, and Compliance team.   to act as an independent assurer of quality and Compliance throughout rb Operations (in the .....
job descriptionwhen you join us at thermo fisher scientific, you’ll be part of a smart, driven team that shares your passion for exploration and Discovery. with revenues of $22 billion and the largest investment in r&d in the industry, we give .....
the wyss zurich is a joint Research and development center of the eth zurich and the University of zurich, which was made possible by a generous donation from the swiss Entrepreneur and philanthropist dr. h.c. mult. hansjörg wyss. the mission of .....
overview the qa manager position provides qa support and oversight to ensure Compliance with Good Clinical Practice (gcp). areas of responsibility include: participate in development of clinical and clinical qa standard operating procedures (sops) .....
Process Engineer – upstream/downstream the ideal candidate for this role will have had 2-3 years of experience support Drug substance Manufacturing Operations through technical investigations and executing technology transfers / new product .....
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