Farmont is announcing a job vacancy:
Quality Assurance and Regulatory Affairs Associate (m/f)
Requirements:
- Bachelor's degree in Pharmacy, Medicine, or Dentistry
- Preferred experience in the registration of drugs and medical devices
- Preferred knowledge of regulations related to drugs and medical devices
- Computer skills (MS Windows, MS Office, Internet)
- Knowledge of English language (written and spoken)
- Preferred driver's license category B
Job description:
- Preparation and maintenance of registration documentation for drugs and medical devices for which an application for marketing authorization is submitted, as well as for supplements, chemicals, biocides for which applications for marketing authorizations are submitted
- Daily communication and information flow with the Medicines and Medical Devices Agency and manufacturers with whom a distribution and/or representation agreement for registration has been concluded
- Monitoring regulatory laws related to the organization's operations and registration of medical devices
- Pharmacovigilance activities
- Responsible for the proper implementation of the quality management system, business processes, and internal audits in accordance with the adopted standards
- Development of necessary procedures related to regulatory affairs pharmacovigilance and medical device vigilance, as well as other procedures as needed
Interested candidates can send their CV to email: office@farmont.me