Understand and support the handling of product lifecycle management and its implications from a Regulatory Affair & Pharmacovigilance (RAPV) perspective.
Manage regulatory-relevant information, ensuring confidentiality and information protection
Assist in providing support for any RAPV project improvements.
Assist with the revision and enhancement of the local registration and PV database.
Provide support in the execution of RAPV tasks, eg :
Template drafting and preparation.
Pharmacovigilance cases monitoring
Handle ad hoc / planned administrative task that are RAPV relevant.
Job Requirements :
Bachelor’s degree in science background such as Animal Husbandry, Animal Science, Biotechnology, Pharmacy or any related fields.
Proficiency in Microsoft office suite.
Analytical and good with integrating information, able to handle paperwork.
Ability to work independently and as part of the team.
High attention to detail and data accuracy.
Strong organizational skills and the ability to manage multiple tasks and deadlines.