Regulatory Affairs Manager APAC
Novonesis Lihat semua pekerjaan
- Kelana Jaya, Selangor
- Tetap
- Sepenuh masa
- Lead and coordinate APAC team, exercising influence‑based leadership to drive collaboration and deliver on RA priorities.
- Lead regulatory submissions, registrations, and market access processes for GMM‑derived Precision Proteins, ensuring compliance for current and new innovations.
- Lead and coordinate APAC regulatory activities across countries, influencing peers and global stakeholders to ensure alignment and delivery.
- Lead regional advocacy and external engagement, collaborating with regulatory authorities, trade associations, and industry groups while monitoring regulatory trends and communicating business impacts.
- Driving execution of regional regulatory strategies in line with global priorities, translating strategy into clear, actionable regional plans.
- Support New Product Development (NPD) by delivering regulatory input and driving regional RA projects in close alignment with global RA teams and policy initiatives.
- Proactively identify, assess, and mitigate regulatory and business risks through Enterprise Risk Management.
- Embed digitalization to enhance APAC RA workflows, enabling efficiency, data‑driven insights, and harmonization of RA best practices and systems.
- Bachelor’s degree or higher in Biology, Biotechnology, Food science, Toxicology, Chemistry, Biochemistry, Genetic engineering or related field.
- Min. 10 years’ work experience in Regulatory Affairs, ideally with exposure to FMCG / Consumer Health/ Ingredients B2B.
- Direct experience and knowledge in Genetically Modified Microorganisms (GMM) are an added advantage
- Proven track record of effective engagement with internal and external stakeholders.
- Fast learner with strong sense of ownership, able to work independently and collaboratively in a matrix organization
- Strong proficiency in English (oral & written).
- Excellent negotiation, communication and influencing skills.