Offer summary

Qualifications:

Bachelor's degree in life sciences or related field is required., Minimum of 5 years of experience in regulatory affairs, preferably in the pharmaceutical industry., Strong understanding of regulatory guidelines and submission processes., Excellent communication and project management skills are essential..

Key responsibilities:

Lead the preparation and submission of regulatory documents to health authorities.

Collaborate with cross-functional teams to ensure compliance with regulatory requirements.

Monitor and interpret regulatory changes and their impact on the organization.

Provide guidance and support to junior regulatory staff and stakeholders.

At Bracco Medical Technologies, every employee has an impact on our Mission to empower lifesaving decisions. We create medical devices that give healthcare providers the insights they need to confidently and safely diagnose patients. Our unique line of products includes Intravascular Ultrasound (IVUS), Fractional Flow Reserve (FFR), Cardiovascular Imaging contrast delivery (CVi), and CT and MRI contrast delivery systems.

Required profile