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1828 jobs

teva is a global Pharmaceutical Leader and the world’s largest generic medicines producer, committed to improving Health and increasing access to quality Health solutions worldwide.  our employees are at the core of our success, with .....
responsibilities department description:the Health safety and environmental group (hse) is responsible for implementing programs and policies that comply with all local, state and federal hse rules and regulations and continuously strive to reduce .....
    position summary the Associate Director, global ds operations lead is responsible for ensuring the proper execution and implementation of drug safty operational activities within global Drug Safety, study management teams, Clinical operations, .....
job description dupont has a rich history of scientific Discovery that has enabled countless innovations and today, we're looking for more people, in more places, to collaborate with us to make life the best that it can be. as a Member of the global .....
solvay is a multi-specialty chemical company committed to developing Chemistry that addresses key societal challenges. we innovate and Partner with customers in diverse global end markets. coatis, one of our business units based in brazil, brings .....
description\:   the Director has responsibility for the Pharmacovigilance Risk Management activities of core strategic * marketed and/or investigational compounds on global level. in additional to reporting to us Line Management, this position .....
correct title: senior manager, trial safety science core work hours - 8 hour day as long as core hours of 9am-4pm are covered. extension of the contract will be contingent upon performance. work site: summit, nj. general responsibilities: • .....
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. .....
at astrazeneca we win through science, it’s at the heart of our every success. that science is only possible when we all work together - we’ll always make sure you’re clear about how your role is connected to our wider mission to really show .....
independently reviews safety-related data from Clinical trials for content, quality, adherence to regulatory guidance and protocols by collecting, analyzing, and triaging Adverse Events as this position impacts product approval, safety signal .....
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