
Regional Regulatory Affairs, Associate Manager
1 week ago
**Position Overview**:As a Regulatory Affairs Manager, you will lead submissions and streamline regulatory processes to ensure product approvals in the APAC/Asia/ASEAN markets, while fostering collaboration and compliance with regional regulations.
**Key Responsibilities**:
- Lead submissions and regulatory responses for new products in APAC/Asia/ASEAN.
- Develop efficient submission strategies for regional regulatory approvals.
- Foster cross-departmental collaboration for regulatory insights.
- Act as the primary internal regulatory contact for the region.
- Standardize regulatory processes to improve efficiency.
- Integrate regulatory information management systems.
- Support innovation and business development projects.
- Monitor regional regulatory changes and assess their impact.
- Gather competitive intelligence on regulatory matters.
**Requirements**:
- 5+ years in APAC/Asia/ASEAN regulatory affairs (pharmaceutical, medical devices, consumer health)
- Experience in new registrations/variations/indications/renewals.
- Degree in Pharmacy, Life Sciences (or in a relevant field).
- Expertise in regional regulatory principals and experience managing communication and collaborations with health authorities.
- Strong multitasking, communication skills and great sense of team-work.
To apply, submit your most updated resume showcasing relevant qualifications and experience.
**Not the right opportunity?**:
We're always looking out for the best talents in the life science industry. If you are currently seeking exciting opportunities within the pharmaceuticals, medical devices, in-vitro diagnostics (IVD), or consumer health industry, do reach out for a confidential chat.
Principal Consultant: Cheong Yee Yin | Registration Number: R22108633 | EA License Number: 17C8502
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