TRABAJO REGULATORY AFFAIRS MEDICAL DEVICE BARCELONA, BARCELONA

medical strategy... regulatory compliance... medical information... medical records... collaborates productively on clinical safety tasks with colleagues from clinical...

We interpret, anticipate, and shape global health authority expectations to build insightful cmc and device regulatory strategies... participate in regulatory execution...

Stay current on regulatory and methodological developments and promote best practices... medical affairs statistician lead - make a global impact in healthcare are...

Requirements: must-have hard skills: proven experience in medical device manufacturing or highly regulated hardware industries... about aurax: aurax is a dynamic...

Participate as medical representative in internal strategic committees... scientifical lead the interaction with regulatory authorities into therapeutical area...

Coordination of medical check-ups... oversee the facility's biosafety management, ensuring adherence to established protocols, regulatory compliance, and promotion...

Clinical development, medical affairs, regulatory affairs)...    experience of global regulatory submissions and interacting with major regulatory agencies...

Clinical operations, pharmacovigilance, medical affairs)... educating clinical staff on regulatory requirements, quality standards and good practices...

Understanding of local regulatory context in spain (tax, medical device pricing laws, vat, etc... liaise with commercial and regulatory teams to align price changes...

Support and contribute to medical monitoring of trials...   p rovide expert scientific input into the preparation of regulatory documents and interactions with...

Choose from the latest ios or android device upon joining (phone or tablet)... full catering for breakfast and lunch at the office  private medical insurance for...

With offices in barcelona, the uk, and china, we support the pharmaceutical, biotech, and medical device supply chains globally... engaging in international projects:contribute...

Provide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities... support and contribute to medical monitoring...

Responsibilities key accountabilities the product security manager key accountabilities are: manage the development and implementation of a comprehensive end-to-end...

Supply chain, customer service, regulatory affairs)... knowledge of pharmaceutical/medical device products, quality processes, and relevant regulations...

Additionally, the role collaborates closely with cross-functional teams to shape tactical plans, navigate regulatory environments, and drive the overall success...

Your main objective will be to lead the development of a delivery system for a medical device, from 2d/3d prototype design to the management of prototype manufacturing...