Twoja przyszła Firma / Your future CompanyNaszym Klientem jest jedna z wiodących, międzynarodowych firm farmaceutycznych, dla której poszukujemy osoby na stanowisko Medical Advisor. Osoba na tym stanowisku, będzie odpowiedzialna za: • Wsparcie w wytyczaniu i realizacji strategii firmy w podległym
medical and scientific product or disease area discussions, and presentations in a non-promotional scientific context. These activities, the circumstances in which they are conducted and the way to perform them in a fully compliant way are described in further detail in the Global MSL Guide. Typical
Are you looking for a patient-focused, innovation-driven company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as a Medical/Scientific Liaison (MSL) - Oncology or Medical/ Scientific Liaison (MSL) - IBD in Poland. Takeda is Accountabilities include: Medical/Scientific Affairs Use specific disease and product knowledge to develop Takeda in a ...
Capgemini is one of the world's foremost providers of consulting, technology and outsourcing services. Cloud Infrastructure Services is one of the biggest outsourcing service providers in Poland. Since the establishment of our first service center in Krakow in 2004, it has achieved great success and grown rapidly. In 2006, we opened a second center in Katowice and in 2012 a third center in Opole ...
Client Service Advisor - English & Turkish (as an asset)Miejsce pracy: Kraków Key Responsibilities: Providing support for High Profile Clients mostly via e-mail and also by phone Advising on the best project practices and understanding client’s needs Ensure that a resolution is provided
THE COMPANY Our client is a professional Medical Devices organization, based in Gelderland Netherlands. This client is operating internationally. They are not responsible for the manufacturing or distribution of products, however they are supporting
Advisor. You’ll be responsible for receiving and responding to clients’ incoming requests as first line support in the Graphic department; Dispatching requests to second line support; Contacting clients via phone, email, and chat exclusively in English; Working in a dynamic environment, in a shift system ...
preferably in a health/life sciences or related field A minimum of 8 years in the pharmaceutical industry Strong understanding of and experience with global medical device-drug combination regulatory approvals; Business travel to be ~10-20% as required
documentation database • Application and implementation of international legislation and documentation REQUIREMENTS • Master in Life Sciences • Minimal 4 years of experience in a RA role within the Medical Devices sector • Excellent knowledge of ISO 13485, particularly
understanding of and experience with global medical device-drug combination regulatory approvals; Business travel to be ~10-20% as required Are you interested and do want to apply for this role, please fill out your application via the apply button
within the Medical devices industry • Evidence of leadership experience and organizational skills • Fluency in Dutch and English • Strong communicator • Experience in working with notified bodies and other authorities Are you interested and
and external audits from the beginning to the end of the process, and making reports of these audits REQUIREMENTS • Bachelor of Life Sciences • Minimal 8 years of experience within the Medical Device industry • Minimal 5 years of experience within a strongly
Euvic - For more than a decade we operate in the area of Information Services. Our team consists of more than 600 IT professionals, and the whole Euvic technology group - which brings together IT companies from all over the Poland - over 1800. We work in 9 premises in Poland and 3 abroad. Euvic runs over 150 various projects implemented in teams consisting from a few to a few dozen people. Our projects are ...
management skills • Excellent understanding of the FDA in particular the 21CFR820 and the MDD • Excellent advisory and consulting skills • Great communicator • Team builder, yet individual decision maker • Fluency in English and Dutch Are you
Minimal 10 years of experience in a Quality role within the Medical Devices sector • Additionally 3 years of experience in a regulatory role • Multiple years of experience as team lead within an international organisation • Excellent knowledge of ISO 13485, risk management, FDA, MDD, and CFR • Excellent
THE COMPANY Our client is a professional Medical Devices organization, based in Brussel Belgium. This organisation is an international market leader developing a wide range of healthcare protection solutions for tons of people across the world. They
within the Medical devices industry • Excellent knowledge of ISO 13485 • Strong organizational and leadership skills • Critical scope and eye for detail • Experience in working with notified bodies and other authorities • Fluency in Dutch and English • Individual, yet team player