... the training plans for Regulatory Affairs within the Language Services department ... localization project manager Strong Regulatory Affairs Labelling experience Strong attention to ... status. If, because of a medical condition or disability, you need ...
... . Research & DevelopmentRegulatory and Safety Affairs is a critical function within ... , local market and intelligence teams, Medical, R&D and commercial cross- ... regard to age, disability or medical condition; colour, ethnicity, race, citizenship, ...
... , Chefs, Factories, Suppliers, Regulatory Affairs, Purchasing for ensuring the availability ... with the Regulatory Scientific Affairs (RSA)brbr* Support to check ... , Chefs, Factories, Suppliers, Regulatory Affairs, Purchasing for ensuring the availability ...
... ., drug safety, regulatory, clinical development, medical affairs) * Extensive knowledge on Global Regulatory ...
... preferably in Clinical Medical Operations Support – Contract Management- Clinical ... e.g., finance, procurement, medical affairs, and external vendors as needed. ... other characteristic) Private medical package with additional preventive healthcare ...
... . Research & DevelopmentRegulatory and Safety Affairs is a critical function within ... , local market and intelligence teams, Medical, R&D and commercial cross- ... regard to age, disability or medical condition; colour, ethnicity, race, citizenship, ...
... the primary contact for Regulatory Affairs in business projects that involve ... the main representative for Regulatory Affairs in business projects involving or ... projects involving or impacting Regulatory Affairs data, systems, and processes. Ensure ...
... , compliance, Regulatory, Pharmacovigilance (PV) and Medical Affairs Responsible and supports development of ... , compliance, Regulatory, Pharmacovigilance (PV) and Medical Affairs Responsible and supports development of ...
... reasons to join our Regulatory Affairs Quality Assurance team: https: www. ... -reasons-to-join-strykers-regulatory-affairs-teamRESPONSIBILITYWhat you will do as ... years of experience in validation.Medical devices experience.Experience working in ...
... or Regulatory experience from the medical device or pharma industry. Furthermore, ... , standards and guidelines within the medical device area e.g. MDR, ... parts of Coloplast - for example Medical Affairs and Manufacturing Sites, and creating ...