Regulatory affairs specialist

On behalf of our client, DEKRA is looking for:

• Regulatory affairs specialist

JOB DESCRIPTION

• Preparation and application of documentation for registration, renewal and variation of drugs and medical devices;
• Categorization and registration of food supplements in the Registar of supplements;
• Regular communication with regulatrou institutions and foreign partners (suppliers);
• Monitorig of adverse drug reactions and submission to the competent institution;
• Ensuring constant maintenance and improvement of the pharmacovigilance system.

QUALIFICATIONS

• Bachelor degree of Pharmacy or Medicine;
• 1-2 years work experience on drug registration, pharmacovigilance;
• Knowledge of local and EU pharmaceutical regulation;
• Solid knowledge of English language;
• Knowledge of MS Office;
• Driving lisence.

ADDITIONAL INFORMATION

If you feel that you have the necessary experience and are interested in this opportunity, please send your CV in English on the following e-mail address: rabota.arbeit.mk@dekra.com

All received applications will be considered in strict confidentiality. Only short-listed candidates will be contacted for an interview.

*By sending your CV and motivation letter, you agree that your personal data will be processed for the needs of recruitment and selection by DEKRA Arbeit Macedonia and they will be stored in the DEKRA database.

Note: Candidates can withdraw their permission to process their personal documents at any time by sending a notification to the e-mail: job.arbeit.mk@dekra.com