TRABAJO REGULATORY AFFAIRS MEDICAL DEVICES BARCELONA, BARCELONA
(18 ofertas de trabajo)
Listado de trabajos de Regulatory affairs medical devices en Barcelona, Barcelona
Regulatory affairs - medical devices
Familiarity with quality assurance procedures for medical devices... at least 2 years of experience in regulatory affairs within the medical device sector...
Regulatory affairs - medical device
Years’ experience in ra - medical deviceknowledge in quality assurance procedures with medical devices... asphalion is growing and we are looking for a regulatory...
Medical device regulatory & quality consultant
Documentation preparation: prepare comprehensive regulatory documentation for medical devices, including ivds and medical device software, ensuring compliance with...
Junior regulatory affairs technician
We are currently looking for a junior regulatory affairs technician to strengthen our regulatory affairs team... any master's degree related to medical devices and/or...
Background regulatorio en entorno farma o medical devices... seleccionamos un/a regulatory affairs para que se incorpore a una multinacional de referencia en anticoagulantes...
Preferred knowledge: regulatory frameworks for medical devices and food supplements... strong cmc technical knowledge with a strategic regulatory mindset...
Medical safety and processes manager
Pharmacovigilance), clinical research, or regulatory affairs solid knowledge in drug safety related processes (incl... the medical safety and processes manager will...
Data and algorithm development engineer
Prepare regulatory documentation and design processes with the quality and regulatory affairs teams to comply with the artificial intelligence regulation and other...
Senior study start up associate
Strong understanding of regulatory requirements and guidelines for clinical trials, including ich-gcp and local regulatory requirements... in addition to your competitive...
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What will you do?we seek an experienced professional in quality assurance and regulatory affairs, with experience in medical devices... solutia life sciences (recruitment...
Clinical project support specialist
The incumbent will work closely with global study team members, and other key stakeholders on a global level to optimize study efficiency, compliance, and quality...
Ability to manage compliance audits, including developing and maintaining documentation for regulatory reviews... create and maintain detailed compliance documentation...
Senior manager, patient engagement, rare disease
Create collaborative relationships with other functional areas and internal stakeholders including, but not limited to, global medical affairs operations, sales...
Associate director, senior patient safety scientist oncology
regulatory reports, health authority responses and the safety content of marketing authorisation applications... patient safety sits within the chief medical office...
Senior clinical study administrator
Collaborating in global initiatives to standardize processes within and across countries (collaboration with other local and global csas) assist with local language...
Research editor, companies ownership research, risk & compliance data
Job description: about the role dow jones risk & compliance is a global provider of third-party risk management and regulatory compliance solutions...
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