Animal Health Regulatory Technician

GRUPO ZENDAL, with more than 25 years of experience, brings together different companies focused on the research, development, manufacturing, and marketing of high value-added products in the health field.

We strive to contribute to the improvement of living conditions through the research, development, and manufacturing of medicines and vaccines focused on the prevention of both human and animal diseases.

At CZ Vaccines, we are looking for a Regulatory Affairs Technician profile oriented towards animal health, with experience in the life sciences industry and the ability to operate in an international environment.

The selected person must have an interest in contributing to the regulatory development and maintenance of biological medicines destined for animal health, as well as a desire to continue growing within the Regulatory Affairs area.

-Manage and maintain the regulatory notifications and registrations of veterinary biological medicines across the different product lines.

-Act as an interlocutor with the competent authorities of the assigned countries, providing support in communications as necessary.

-Review scientific and clinical literature to support product registrations and continuous regulatory compliance.

-Keep regulatory registrations and databases up to date, as well as the registration requirements for each country and the product documentation files.

-Monitor current and future regulations, standards, and guidelines that affect the business, and communicate key updates to the Regulatory Affairs team.

-Provide regulatory support for tenders, ensuring complete responses while meeting established deadlines.

-Represent the Regulatory Affairs department in internal and external meetings, including those of industry associations, following up on agreed actions.

-Provide regulatory support at a regional level, keep shared platforms up to date, such as network drives and SharePoint, and periodically report progress to the EMEA Regulatory Affairs team.