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responsibilities job descriptionjob title:  scientific commodity manager, Lab equipment, north americadate: july 2018entity: scientific & Clinical procurementlocation: westboro, mareporting to:  s&c Procurement regional head, americasreporting to .....
with minimal supervision, write and edit Clinical documents needed for regulatory purposes (eg, protocols, study reports, high level summary documents, Investigator brochures, briefing documents) for submission within established timelines to .....
with minimal supervision, write and edit Clinical documents needed for regulatory purposes (eg, protocols, study reports, high level summary documents, Investigator brochures, briefing documents) for submission within established timelines to .....
passion for Innovation. compassion for patients.™ daiichi sankyo entwickelt und vermarktet mit 15 000 mitarbeitern in über 20 ländern innovative arzneimittel für patienten. wir verfügen nicht nur über ein starkes portfolio von arzneimitteln .....
job descriptionposition summary: the candidate will be expected to support Researcher in executing routine chemical Analysis of a wide range of products in accordance to standard operating procedures (sops) and good Laboratory practices. he/she must .....
job descriptionjob title:  scientific commodity manager, Lab equipment, north americadate: july 2018entity: scientific & Clinical procurementlocation: westboro, mareporting to:  s&c Procurement regional head, americasreporting to this position: .....
job descriptionposition summary: the candidate shall have intermediate experience (practical or academic) in scientific Laboratory work running routine validated test methodologies and be able to perform Data Analysis all under good Laboratory and .....
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 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 .....
for current gilead employees and contractors: please log onto your internal Career site to apply for this job. job description gilead’s pathobiology group provides intellectual and experimental input across all of R&D to enhance Discovery, .....
973 jobs

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