Regulatory Affairs Professional

5 days ago


Stockholm, Stockholm, Sweden TN Sweden Full time

We are seeking a Regulatory Affairs Manager to join our Medical department at TN Sweden. This role offers an exciting opportunity to work in a dynamic and fast-paced environment, collaborating with cross-functional teams to ensure regulatory compliance.

The successful candidate will have a strong background in regulatory affairs, excellent communication skills, and the ability to think strategically. We are looking for someone who can develop and implement regulatory strategies to support business objectives.

Main Responsibilities:

  1. Regulatory Strategy Development:
  • Develops and implements regulatory strategies to support business objectives.
  • Collaborates with cross-functional teams to ensure regulatory compliance.
Policy Monitoring:
  • Monitors regulatory developments and updates policies accordingly.
  • Provides guidance to employees on regulatory requirements.
Cross-functional Collaboration:
  • Works closely with marketing teams to ensure regulatory compliance of marketing materials.
Communication with External Partners:
  • Main point of contact for external partners and regulatory authorities.
  • Submits regulatory documents and responses to requests for information.

Qualifications & Skills:

  • MSc of Pharmacy or other relevant degree in natural sciences.
  • Minimum 2 years of experience in Regulatory Affairs.
  • Strong knowledge of regulations for medicinal products and/or medical devices.
  • Excellent communication and interpersonal skills.
  • Proven ability to lead regulatory submissions and interactions with regulatory agencies.
  • Fluent in English.
  • Merit: Experience from both MedTech and pharmaceutical industry.


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