Sr. Clinical Project Manager (m/f/d)
Deutschland
Vollzeit
Abiomed
… the Senior Clinical Program Manager, Clinical Research Associates, Medical Affairs and Regulatory Departments to execute the trial. This role will engage and … Program Manager, Clinical Research Associates, Medical Affairs and Regulatory Departments to execute the trial. This role will engage and work closely … Primary Duties and Responsibilities: Responsible for comprehensive study management for clinical study, for example protocol and database development, site …Affairs StellenangeboteQuality Engineer (m/f/d)
München
Vollzeit
LivaNova
… Knowledge is use of statistical application tools e.g., Minitab Regulatory Affairs knowledge is preferable Pragmatic and result-oriented: autonomous, … Quality Engineering pertaining to external suppliers‘ activities Support regulatory audits on site What are we looking for To successfully execute the … verification and validation testing, production line testing, and risk management process for new generation devices as well as life cycle management of …Regulatory Management StellenangeboteRegulatory Affairs Specialist
Frankfurt am Main
Vollzeit
PrimeVigilance
… services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class support to our … Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class support … Job Responsibilities Ensure the effective and rapid coordination and management of project deliverables to meet the agreed targets and to comply with the …Regulatory Affairs Management Stellenangebote
Junior Clinical Research Associate
München
Vollzeit
AstraZeneca
… and assisting with feasibility activitiesCollaborating with local Medical Affairs and other internal stakeholders, as neededFollowing quality issue … some countries, as required, CRAs are accountable for study startup and regulatory maintenance; tasks may include collection, preparation, review and … works in close collaboration with other CRAs and the Country Operations Management (COM) Team to ensure that study commitments are achieved in a timely and …Regulatory ManagementPackaging & Labeling Specialist (m/f/d)
Biberach an der Riß
Vollzeit
Randstad Deutschland
… Autonomously work in conjunction with CTSU Trial teams, Regulatory Affairs, Global Randomization, Medicine and label vendors to create, define and … much more) Ihre Aufgaben Review of Master Label Text drafts considering regulatory requirements, standard text phrases and trial specifics Prepare country … completed label documentation for final release to the Release and Process Management Team Global PLC-L Specialist provides all relevant Documents like Master …Regulatory Affairs ManagementGlobal Pharmacovigilance Operations Lead (f/m/d)
Garching bei München
Vollzeit
ITM Isotope Technologies Munich SE
… (Clinical Operations, Clinical Science, Data Management, Medical Affairs) and external vendors What we offer: A modern workplace and exciting … safety procedures and processes including clinical and post-marketing regulatory reporting requirements Support and/or provide assistance in product filing … inspection readiness from a PV Operations perspective Organize and record management of PV documentation and procedural documents (eg. Safety management Plans, …Regulatory StellenangeboteSenior Manager (f/m/d) Clinical Affairs
Bayern
Vollzeit
Siemens Healthineers
… Then come and join our global team asSenior Manager (f/m/d) Clinical Affairs to support our Business Areas/Lines, Business Horizontals and Technology … or a contract research organization You have profound knowledge of the regulatory requirements for medical devices and IVDs and are proficient in the most … experience in Post Market Clinical Follow Up You have experience in the management and monitoring of clinical trials and/or (clinical) performance evaluation …Regulatory Management StellenangeboteProduct Change Manager*
Norderstedt
Ausbildung
Schülke & Mayr GmbH
… Bereichen Product-Management, Product-Life-Cycle Management, Regulatory Affairs, Supply-Chain, Operations, Quality und dem Technical Innovation Center … den internen Bereichen Product-Management, Product-Life-Cycle Management, Regulatory Affairs, Supply-Chain, Operations, Quality und dem Technical Innovation … bringen Sie alle notwendigen Aktivitäten im Rahmen des Product-Life-Cycle-Managements in Einklang mit den relevanten technischen und regulatorischen …Regulatory ManagementSpeculative job application for KLS Martin Group
Tuttlingen
Vollzeit
KLS Martin Group
… fields: Sales Logistics/Disposition Purchasing Quality/Regulatory Affairs Production/Technology Development/Design What we offer Customized … in the following fields: Sales Logistics/Disposition Purchasing Quality/Regulatory Affairs Production/Technology Development/Design What we offer Customized … Customized familiarization Education and training Flexible working Health management Cafeteria Pension plan and insurance Growth in a family-owned company …Regulatory Affairs ManagementManager Regional Affairs Central Europe
Frankfurt am Main
Vollzeit
International Air Transport Association (IATA)
… Duration: About the team you are joining Reporting to Director, Regional Affairs Europe, the incumbent will execute and contribute to designing IATA's … advocate and lobby key IATA positions to the national governments and regulatory authorities including general legislative, regulatory and policy … attitude; Strategic mindset; Strong communication skills, relationship management, as well as well-developed negotiation, presentation and lobbying skills; …Affairs StellenangebotePharmaceutical Internship (f/m/d)
Schwalbach am Taunus
Vollzeit
Procter & Gamble
… international environment together with other departments like Regulatory Affairs, Marketing, Legal, Quality etc. on product ideas, product offers, … work in an international environment together with other departments like Regulatory Affairs, Marketing, Legal, Quality etc. on product ideas, product offers, … we offer you the possibility to work on diverse tasks related to Quality Management systems in the Healthcare sector and applicable for Rx, Over-the-counter …Management StellenangeboteDesign Quality Assurance Expert (m/w/d)
Bad Homburg vor der Höhe
Vollzeit
Fresenius Medical Care
… years of professional experience in research and development, regulatory affairs or quality management for medical devices or pharmaceuticals Advanced … Ensure that all design control deliverables comply with applicable regulatory requirements and design controls SOPs Provides input and guidance to … Design Quality Review and approve all product development and change management projects compliance with Fresenius Quality management System / SOP …Affairs ManagementPackaging & Labeling Specialist (m/f/d)
Biberach an der Riß
Vollzeit
Randstad Deutschland
… Autonomously work in conjunction with CTSU Trial teams, Regulatory Affairs, Global Randomization, Medicine and label vendors to create, define and … much more) Ihre Aufgaben Review of Master Label Text drafts considering regulatory requirements, standard text phrases and trial specifics Prepare country … completed label documentation for final release to the Release and Process Management Team Global PLC-L Specialist provides all relevant Documents like Master …Regulatory Management StellenangeboteProject Manager R&D (f/m/x)
Oberkochen
Vollzeit
ZEISS Group
… other departments including: Product Management, Sourcing, Regulatory Affairs, Quality Management and all disciplines within R&D Establish, develop, … with other departments including: Product Management, Sourcing, Regulatory Affairs, Quality Management and all disciplines within R&D Establish, … including: Product Management, Sourcing, Regulatory Affairs, Quality Management and all disciplines within R&D Establish, develop, and maintain supplier …Regulatory Affairs Stellenangebote