• Multinational Healthcare Company
• International project

¿Dónde vas a trabajar?

This opportunity is with a large organization in the Healthcare industry that is known for its commitment to innovation and quality. With a strong presence in its field, the company offers a professional environment to thrive in regulatory affairs.

Descripción

• Prepare and submit regulatory documentation for product approvals.
• Contribute to international regulatory submission strategies.
• Ensure compliance with applicable regulations and standards in the Healthcare industry.
• Collaborate with cross-functional teams to support product development and registration.
• Maintain up-to-date knowledge of regulatory requirements and changes.
• Coordinate with regulatory authorities as needed for product approvals.
• Provide guidance to internal teams on regulatory processes and best practices.
• Review and approve product labelling and promotional materials for compliance.
• Support audits and inspections related to regulatory affairs.

¿A quién buscamos (H/M/D)?

A successful Regulatory Affairs professional should have:

• Educational background in life sciences, pharmacy, or a related field.
• Minimum 5 years of experience in pharmaceutical or medical devices industry working as a Regulatory Affairs Specialist.
• Knowledge of regulatory requirements in the industry.
• Strong attention to detail and organizational skills.
• Ability to work collaboratively with cross-functional teams.
• An advances English level is a must.

¿Cuáles son tus beneficios?

• Competitive salary range.
• Permanent contract based in the north of Madrid.
• Opportunities to grow within the Multinational company.
• Professional development and training programs.
• Supportive company culture focused on innovation and quality.