The main duties & responsibilities would include:

- Track of status and progress of regulatory documentation.
- Review, edit and proofread regulatory documentation.
- Assist in preparation and review of labelling and other departmental documents.
- Support local marketing by means of timely and effective communication.
- Compile under supervision regulatory documents for submission.
- Participate as an active team member of project teams as required.
- Compile and prepare responses to regulatory authorities questions.
- Maintain regulatory files in a formal consistent with requirements.
- Maintain awareness of regulatory requirements.
- Maintenance of e-catalogue (approve “pending approval” codes by validating defined product features)
in collaboration with the divisions.


Requirements:

- Life science degree (medical, paramedical, pharmacy, biochemistry field is preferred)
- At least 1-2 years experince in Regulatory Affairs
- Good organizational skills with ability to work diligent, accurate and under pressure, alone or as part of a team
- Good communication skills
- Fluency in Estonian and English, both written and spoken


If you are interested in this position or know someone who might be suitable/interested, please feel free to contact me or pass my contact details for further information.


SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business