Regulatory Affairs Specialist

4 semanas atrás


Lisboa, Lisboa, Portugal Abbvie Tempo inteiro
Role Overview

We are seeking a highly skilled Regulatory Affairs Specialist to join our team at AbbVie. In this role, you will be responsible for ensuring the maintenance of Marketing Authorisations for medicinal products and Medical Devices registrations through variations and other regulatory submissions.

About the Role

The ideal candidate will have a life sciences degree and a minimum of 5 years of experience in Regulatory Affairs in the pharmaceutical industry. They should have strong knowledge of information management and database administration, as well as excellent communication skills in English.

Key Responsibilities
  • Maintain awareness of current and new legislation/guidance and ensure compliance with all relevant statutory requirements and internal procedures.
  • Liaise with national regulatory authorities to obtain optimal outcomes for patients and AbbVie's portfolio.
  • Review promotional and non-promotional materials for compliance with local legislation and corporate requirements.
Benefits

We offer a competitive salary range of $80,000 - $120,000 per year, depending on experience, plus benefits including health insurance, retirement plan, and paid time off.

What We Offer

AbbVie is an equal opportunity employer committed to diversity and inclusion. We strive to create an inclusive work environment that values diverse perspectives and backgrounds. If you are passionate about working in Regulatory Affairs and have a strong desire to make a difference in people's lives, we encourage you to apply for this exciting opportunity.



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