About Alivira
Alivira Animal Health is one of the world's leading animal health companies, operating in more than 90 countries. With a strong manufacturing infrastructure and an innovative R&D approach, Alivira delivers products and services of high quality standards to customers worldwide through its production facilities and R&D centers located in India, Brazil, Turkey, and Spain.
With a focus on animal health and welfare, Alivira operates with a broad product portfolio for both companion animals and farm animals. The company manufactures a wide range of product groups, including sterile injectable antibiotics, non-steroidal anti-inflammatory drugs (NSAIDs), sterile injectable vitamin and mineral preparations, hormone products, antibiotic aerosols, endectocides, and sera.
The high-capacity production facility of Alivira's Turkey operations holds an important position in the sector thanks to its manufacturing processes compliant with international quality standards and its advanced technological infrastructure. In addition, drawing on the knowledge and experience it has gained since 1975, Alivira continues to add value to the sector by extending this expertise into areas such as animal health management, preventive veterinary medicine practices, and phytogenic (plant-based) solutions that support animal welfare.
With its global organizational structure, sustainable growth vision, and scientific approach, Alivira Animal Health is among the leading companies offering reliable and innovative solutions in the animal health sector.
We are looking for an International Registration Specialist with the qualifications listed below, to be employed in the Registration (Regulatory Affairs) Department at our Head Office located in Istanbul, Kartal.
General Qualifications
- Graduate of a Faculty of Veterinary Medicine,
- Preferably at least 2 years of experience in the animal health, veterinary medicinal products, or pharmaceutical sector,
- Experienced in monitoring quality and registration/licensing regulations, documentation, and official correspondence,
- Detail-oriented, careful, and possessing strong analytical thinking skills,
- Good command of English,
- Proficient in MS Office applications,
- Strong follow-up skills, results-oriented, and able to work well within a team,
- For male candidates, having completed military service,
- Residing in Istanbul, Kartal, or able to commute without difficulty,
Duties and Responsibilities
- Managing and following up on the registration (marketing authorization) processes of veterinary medicinal products,
- Preparing the necessary documentation for registration applications, variations, renewals, and other official procedures,
- Checking application files for compliance with regulations,
- Conducting correspondence with relevant public institutions and official authorities,
- Monitoring regulatory changes related to registration processes and informing the relevant units,
- Supporting the preparation of technical and scientific documents,
- Ensuring that all records related to the registration process are archived in an organized and complete manner,
- Ensuring coordination with relevant internal departments.
Preferred Qualifications
- Experience in veterinary medicinal product registration processes,
- Familiarity with the regulations of the Ministry of Agriculture and Forestry,
- Knowledge of CTD/eCTD documentation.
Want to join our team - aplly to this link and upload your CV in English
https://alivira.cvw.io