RA Principal Associate

3 giorni fa

Remote, Italia K-Recruiting GmbH Tempo pieno
RA Principal Associate (M/F/X)
Verifichi che le sue competenze e la sua esperienza corrispondano ai requisiti di questo ruolo, quindi si candidi con il suo CV qui sotto.
Tasks:

  • Lead and execute regulatory strategies for assigned products and projects.


  • Prepare, compile, and submit high-quality regulatory applications, including variations, renewals, and responses to health authority questions.


  • Ensure regulatory dossiers remain compliant and up to date for EU, UK, and Switzerland markets.


  • Provide regional regulatory expertise to support global development, CMC, compliance, and labeling activities.


  • Liaise with regulatory authorities and support regulatory agency interactions.


  • Collaborate with cross-functional stakeholders including Regulatory Affairs, Quality, Medical, Pharmacovigilance, Commercial Operations, and Business Development teams.



Qualification:

  • Degree in Biological Sciences, Pharmacy, Allied Medical Discipline, or related field (advanced degree preferred).


  • Minimum 5+ years of Regulatory Affairs experience within the pharmaceutical or biotechnology industry.


  • Strong experience with regulatory submissions and registrations in the EU, UK, and Switzerland.


  • Experience managing regulatory applications, variations, renewals, and health authority interactions.


  • Exposure to Veeva and regulatory application management systems is highly desirable.


  • Experience in vaccines and/or biologics is advantageous. xysqume


  • Strong project management, stakeholder management, and communication skills.


  • English proficiency is required as all Seqirus business is conducted in English



Requirements:

Start : Within the next four weeks


Duration : 6 months


Capacity : 5 days per week


Location : Tuscany (IT)


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