Plaats Job

155 Jobs voor regulatory affairs manager

Ontvang JobAlert
RA Specialist AD

...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...

Quality Systems Specialist AD

...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...

RA Specialist AD

...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...

RA Specialist

...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...

Director of Quality

...regulatory audits, inspections, and CAPA processes, ensuring global readiness and compliance Drive continuous improvement initiatives and risk‑based quality management Collaborate closely with R&D, Re...

Director of Public Affairs

...Affairs Strategies Lead the development and implementation of public affairs strategies to effectively manage relationships with government bodies, regulatory agencies, and other external stakeholders...

Quality systems specialist

...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...

RA Specialist

...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...

Quality Systems Specialist

...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...

Quality Director

...Regulatory Inspections & Audits Manage preparation and response for regulatory inspections (FDA, EU QP, WHO, etc.). Liaise with regulatory agencies during inspections and audits, ensuring prompt, tran...

Quality Systems Specialist

...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...

RA Specialist

...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...

Head of Quality Assurance

...regulatory guidelines and ensure adherence to applicable regulations such as GMP, GLP, and GCP, with specific consideration of ATMP regulations. Collaborate with regulatory affairs teams to support su...

RA Specialist AD

...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...

Quality Systems Specialist AD

...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...