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You’re looking for Safety Fo jobs . On BrightOwl, we centralise vacancies from biotech, pharma and life sciences companies in general. Register for free, build your profile so that companies can contact you for new openings.

3340 jobs

manager, Drug Safety aggregate reporting – Pharmacovigilance r&d – malvern, pa about endo international plcendo international plc (nasdaq: endp) is a highly focused generics and specialty branded Pharmaceutical company delivering quality .....
requisition id: dru000895for our global Clinical safety & Pharmacovigilance department we are currently Recruiting a: Director, deputy Qualified Person for pharmacovigilancebased in brussels or another eu-country (except united kingdom)the .....
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 .....
    position summary the senior manager, safety Scientist plays a pivotal role within global Pharmacovigilance to ensure safety assessment for all alexion products, in close collaboration with the product assigned global medical safety .....
nestlé skin Health is a global Leader in improving the quality of life by delivering innovative medical solutions for the Health of skin, hair and nails throughout people's lives. nestle skin Health aims to meet the needs of Healthcare .....
    position summary responsible and accountable for all aspects related to the handling of safety information originating from post-Marketing, Clinical trials, literature, and other sources. investigation, Documentation, Medical Research, and .....
job description dupont of circleville has openings for a rd Leader, kapton® Formulation technology.  the circleville site is located approximately 30 miles south of columbus, oh and manufactures kapton® film, tedlar® film, teflon® film, .....
    position summary responsible and accountable for all aspects related to the handling of safety information originating from post-Marketing, Clinical trials, literature, and other sources. investigation, Documentation, Medical Research, and .....
description of the area:global quality (gq) – Clinical trials and safety, gq-ct&s is responsible for Auditing all processes related to Clinical research including specific medical affairs processes, and Pharmacovigilance activities, to assess .....
the position major responsibilities:Partner closely with safety assessment scientists to envision, implement, and support Informatics tools and Business Process that enhance our ability to acquire, store, transform, visualize and analyze nonclinical .....
3340 jobs