Regulatory Affairs Specialist – ATMP

At QbD our RA Services go from regulatory strategy, clinical, CTD registration dossier writing, eCTD compilation and submission to competent authorities to Vigilance. We support from idea to commercialization. Do you want to ensure the organization’s compliance with the regulations and laws regarding ATMP’s? Do you want to guide them through complex regulatory requirements and […]

Clinical Regulatory Manager

WHAT ARE YOUR MAIN RESPONSIBILITIES?  Responsible for management and coordination of the clinical regulatory submission team (EC and CA submissions in EU), ensuring a smooth process from submission through approval, striving to the highest quality standard in a timely and efficient way. Main Responsibilities: Advice & Expertise: Being a subject matter expert who provides guidance […]

Performance Evaluation Studies Expert

Hi there, who are you?  Are you excited about science and technology? Do you love to dig into scientific data to investigate the performance of that new diagnostic test? Do you enjoy coordinating and making sure the job gets done according to plan? Are you looking for a job that allows you to help other […]

Regulatory Affairs Specialist – Medical Devices

At QbD our RA Services go from regulatory strategy, clinical, technical file to Vigilance. We support from idea to commercialization. Do you want to support companies throughout the entire medical device regulatory lifecycle? Do you want to guide them through complex regulatory requirements? This all in an efficient and pragmatic way? Then apply now! What […]