Regulatory Affairs Specialist

1 giorno fa

Remote, italia Accord Healthcare Tempo pieno

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Job Title: Regulatory Affairs Specialist

Job Requisitions No.: 18302

Job Description:

Role Details

The role has primary responsibility for supporting all local regulatory affairs workflow including preparation of dossiers and applications for new registration and maintain existing products life-cycle as well as applying the pharmacovigilance policy under the supervision by line Manager.

The Role

Support RA and QA team in:

  • Preparation of dossiers and applications to register new products and maintain existing products life- cycle
  • Preparation of parallel import applications for national and central import procedures.
  • Supporting the relationships with local regulatory authorities to achieve positive outcomes for new product registrations, variations, renewals, notifications.
  • Submission of Life Cycle Management changes (variations, marketing status, sunset clause, renewals and line extensions)
  • Artwork revision process, i.e. requesting, proof reading, approval and implementation of artwork
  • Close cooperation with supply chain and marketing department to ensure product launch and marketing materials approval from regulatory perspective.

The Person

  • At least 6 months 1 -year professional experience on similar position or internship in RA Department in pharmaceutical company or national competent authority
  • Knowledge of pharmaceutical law and the required documentation for pharmaceutical product

The Rewards

A Bit About Us

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All applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability.

Requisition ID: ((id))

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