Regulatory Affairs Specialist

We are seeking a skilled Regulatory Affairs Professional to oversee the registration of medicinal products across Europe and national submissions. The ideal candidate will have experience in devising submission strategies, assigning due dates, and ensuring timely completion.

Key Responsibilities

• Develop and implement submission strategies for each project, ensuring compliance with regulations and laws.
• Coordinate document preparation for regulatory submissions, including package design and content creation.
• Collaborate with external partners to expedite submissions and ensure seamless communication.

Candidate Requirements :

Desirable Skills :

Benefits

This role offers the opportunity to work in a fast-paced environment, driving new opportunities for growth and development. Our collaborative culture values innovation and encourages employees to take ownership of their work.

We offer ongoing training and development opportunities, supporting our team members in achieving their career goals. If you are a motivated and experienced professional looking for a new challenge, please apply.