Jobs 2571 bis 2580 von 5.805 (dupliziert 4.661)
Regulatory & Quality Affairs Manage - QMS Medical De...
PharmiWeb - Beelitz
Compilation of technical documentation according to MDR 2017/745 Annex II Knowledge and skills: Completed training or studies in the fields of natural sciences, Medical technology, engineering or comparable training backgroundVor 60+ Tage
Market Access Senior Associate
PharmiWeb - Beelitz
experience in business consulting with a focus on Healthcare, in the pharmaceutical industry or in other areas of the healthcare industry Knowledge of market access and pricing & reimbursement for pharmaceuticals, Diagnostics andVor 60+ Tage
PharmiWeb - Beelitz
attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues. Participate in preparation and management of research budgets and negotiations. Requirements: Extensive OncologyVor 60+ Tage
PharmiWeb - Suhl
knowledge Software OR Electronic Device experience I specialise in recruiting Regulatory Affairs professionals throughout Europe, if you would like to speak to me regarding the above position then please call me today on +44Vor 60+ Tage
PharmiWeb - Hamburg
launch of 2 new products Support in Risk Management of Class 1 Devices - ISO 14971 Providing Regulatory knowledge and support in MDD - MDR Suitable candidates will have experience in: 4 years' Risk ManagementVor 60+ Tage
Germany Based Biological Evaluation Manager Wound Care
PharmiWeb - Beelitz
experience in the medical device industry(wound management ideal) Experience in the implementation/contracting/evaluation of analyses and tests Knowledge of the Medical Devices Act and related specialist areasVor 60+ Tage
PharmiWeb - Heidelberg
Experience working at trial sponsor and overseeing CROs preferred. Basic SAS knowledge including data import and export. Demonstrable multitasking, project management, and execution skills. Good interpersonal skillsVor 60+ Tage
Hobson Prior - Frankfurt am Main
quality system and units. Profound knowledge of current GCP regulations and best practices, as well as experience in FDA and EMA inspections. Experience with global late stage clinical trials leading to marketVor 60+ Tage
Eu-startups - Bielefeld
Knowledge about the media and experience with the implementation of cross-media design solutions ranging from conceptualizing and drafting it up to final artworks/ data input A sixth sense for design, typo and imagery besidesVor 60+ Tage
Director of Quality Management
Hobson Prior - Rostock
in a laboratory operation (biotechnology or medical diagnostic). Knowledge of GLP, GMP, ISO15185, ISO13485, ISO9001 and of CAP and CLIA. Apply now: If you are interested in learning more or applying to thisVor 60+ Tage