REGULATORY AFFAIRS SPECIALIST

To support obtaining authorization/permit/approval in line with the legal regulations in Turkey in order to market all product ranges (for pharma and medical device) of company and ensure market continuity.

Handling the preparation of the registration files in high quality to submit to the MOH within the pre-defined KPIs

Ensuring that the Company’s products comply with the regulations of the local Health Authority

Speeding up the initiation of the registration procedures.

To shorten the registration period for quick access to the market with the favorable labelling information.

To be a deputy Local Vigilance Represantative of the Company and report incoming complaints in compliance with in-house and MoH requirements by following up a sistematic approach