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 […]

Senior Project Manager Life Sciences

As a QbD project manager you are our leader for projects within our focal points: Advanced Therapy Medicinal Products (ATMP), biotech sector and/or medical devices area. Up for a challenge within the most innovative environments of the life science sector? Keep on reading! What are your responsibilities as a project manager (PM)? You are responsible […]

Regulatory CMC Writer

Do you have a passion for technical, scientific writing? Do the words “responsible, communicative & effective” fit you perfectly? Then don’t hesitate and apply for this position!

Regulatory affairs consultant

Do you want to ensure the organization’s compliance with the regulations and laws regarding drugs and medical devices? Then you are the perfect RA specialist!