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22 jobs

description was unsere mitarbeiter auf der ganzen welt verbindet, ist ihr tägliches engagement, um leben zu retten und zu erhalten. unsere tägliche arbeit ist für viele menschen von großer bedeutung. wollen auch sie wissen, warum es so .....
at abbott, we're committed to helping you live your best possible life through the power of Health. for more than 125 years, we've brought new products and technologies to the world -- in Nutrition, Diagnostics, Medical Devices and branded generic .....
cordenpharma international corden pharma international gmbh corden pharma is an Expert contract Manufacturing Partner, enabling Pharmaceutical and Biotechnology companies to link their requirements for product success with their patients’ .....
cordenpharma international corden pharma international gmbh corden pharma is an Expert contract Manufacturing Partner, enabling Pharmaceutical and Biotechnology companies to link their requirements for product success with their patients’ .....
Ridgefield, CT location   Description\:   Responsible for development, review, finalization, and maintenance of informed consent and other relevant patient documents, processes, and standards for assigned US clinical trials in accordance .....
are you looking for a new professional challenge and are you interested to work in an international team with attractive prospects at a successful Pharmaceutical company, which has been named “best employer” several times?   as .....
What to expectAs Manager Quality System you are an expert in ISO 13485 implementation at our medical device company. Together with your team you will interact with Brainlab departments and partners internationally to manage compliance of our .....
job purpose:as required by the German drug law (amg), German regulation “arzneimittel- und wirkstoffherstellungsverordnung (amwhv)”, the Clinical Trial directive 2001/20/ec and annex 13 to the european GMP guide, all investigational medicinal .....
Tasks & responsibilities   In this role you will be responsible for ensuring that validation-relevant systems within Global Pharmacovigilance are in a validated state at all times of their system lifecycle, that validation is performed .....
Your Responsibilities: Leads Clinical Trial Team (CTT) in operationalizing protocol Creates trial level timelines and ensures all trial deliverables are met with high quality on time and within budget Ensures all trial related documents including .....
22 jobs