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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 .....
shire is the leading global Biotechnology company focused on serving people with rare diseases and other highly specialized conditions. we have best-in-class products available in more than 100 countries across core Therapeutic Areas including .....
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 .....
biolife’s employment opportunities are among the best, offering competitive pay, immediate benefits, paid time off, on the job Training, advancement potential and an environment full of fast-paced fun all while working to save .....
purpose/objective of the jobthe ad of gq ct&s risk assessments is an essential role to lead the enterprise risk assessments related to Clinical trials. this role reports to the head of gq ct&s quality governance and risk assessments.key .....
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: • .....
responsibilities job summary: the oversight Clinical Project Leader (ocpl) is responsible for the functional oversight of field-based cras in a given region. the ocpl ensures that adequate resources are available to support the Clinical Trial .....
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 .....
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