Regulatory Affairs Associate

**Responsibilities**:

- Compilation and submission of product registration dossiers in assigned Asia Pacific countries
- Conduct hazard and formula assessments on formulated products
- Maintain and renew existing product registration to ensure no interruption to license under his/her portfolio
- QA: assist in importation/batch release and GDP locally
- PhV: implement the future PhV system in the responsible region
- Set up good regulatory network by establishing relationships with regulatory bodies in assigned countries (incl. Indonesia, Philippines and others when assigned)
- Stay vigilant and keep abreast of the regulatory changes (veterinary biological product regulations)
- Ensure that Kemin’s Intellectual properties are protected

Qualifications:

- Degree in Science (preferably Veterinary medicine, Chemistry, life science) or its equivalent.
- Mature, preferably with a few years of working experience
- Experience in regulatory affairs would be an added advantage
- Experience in authoring of Safety Data Sheets (SDS) for Asia Pacific countries would be preferred
- Meticulous, with good organizational and IT skills
- Self-motivated, maintains confidentiality and able to work independently with mínimal supervision
- Enjoys multi-tasking and willing to handle administrative and paperwork