Take ownership of regulatory dossiers from A-Z for veterinary medicines, including registrations, renewals and variations for a defined group of countries.
Prepare, maintain and update regulatory documentation, translating scientific product information into complete and compliant registration files.
Work closely with QA and QC and other departments to align documentation, support compliance activities and help determine the right regulatory approach per product or market.
Act as a regulatory point of contact for internal teams and external agents, handling questions related to registrations and ongoing dossiers.
Support the practical regulatory process on-site, including handling samples and ensuring documentation flows smoothly between teams.
WHAT OTHERS SAY
Reviews from the
team
No data was found
ABOUT THE TEAM
Inside
Take ownership of regulatory dossiers from A-Z for veterinary medicines, including registrations, renewals and variations for a defined group of countries.
Prepare, maintain and update regulatory documentation, translating scientific product information into complete and compliant registration files.
Work closely with QA and QC and other departments to align documentation, support compliance activities and help determine the right regulatory approach per product or market.
Act as a regulatory point of contact for internal teams and external agents, handling questions related to registrations and ongoing dossiers.
Support the practical regulatory process on-site, including handling samples and ensuring documentation flows smoothly between teams.
ABOUT THE LOCATION
Life in
Take ownership of regulatory dossiers from A-Z for veterinary medicines, including registrations, renewals and variations for a defined group of countries.
Prepare, maintain and update regulatory documentation, translating scientific product information into complete and compliant registration files.
Work closely with QA and QC and other departments to align documentation, support compliance activities and help determine the right regulatory approach per product or market.
Act as a regulatory point of contact for internal teams and external agents, handling questions related to registrations and ongoing dossiers.
Support the practical regulatory process on-site, including handling samples and ensuring documentation flows smoothly between teams.
WHAT MAKES IT UNIQUE
Why this role
stands out
Take ownership of regulatory dossiers from A-Z for veterinary medicines, including registrations, renewals and variations for a defined group of countries.
Prepare, maintain and update regulatory documentation, translating scientific product information into complete and compliant registration files.
Work closely with QA and QC and other departments to align documentation, support compliance activities and help determine the right regulatory approach per product or market.
Act as a regulatory point of contact for internal teams and external agents, handling questions related to registrations and ongoing dossiers.
Support the practical regulatory process on-site, including handling samples and ensuring documentation flows smoothly between teams.
BENEFITS
Benefits at
Interchemie
Take ownership of regulatory dossiers from A-Z for veterinary medicines, including registrations, renewals and variations for a defined group of countries.
Prepare, maintain and update regulatory documentation, translating scientific product information into complete and compliant registration files.
Work closely with QA and QC and other departments to align documentation, support compliance activities and help determine the right regulatory approach per product or market.
Act as a regulatory point of contact for internal teams and external agents, handling questions related to registrations and ongoing dossiers.
Support the practical regulatory process on-site, including handling samples and ensuring documentation flows smoothly between teams.
