Join our dynamic team where innovation and care converge in a culture that values continuous learning, diversity and transformative career development. Underpinned by THRIVE with Zuellig Pharma, our commitment to transforming the way we grow, care and succeed together as one organization, we are dedicated to helping our people make a meaningful impact in healthcare.
Regulatory Affairs Manager
Requisition ID:
2128
Posting Start Date:
10 Sept 2026
Location:
Sun Valley, Philippines
- Evaluation and preparation of dossiers and technical documents for submission of new pharmaceutical and healthcare products
- Ensure regulatory compliance of pharmaceutical and healthcare products throughout the product’s lifecycle
- Identify risks and gaps that may impact implementation of local regulatory and commercialization plans
- Develop innovative regulatory strategy to drive competitive advantage
- Communicate and coordinate with various stakeholders (partners, cross-functional team, regional team, etc.) on regulatory status and updates
- Represent company with various Regulatory Health Authorities (FDA, PDEA, BAI, etc.)
- Prepare and review of artworks and labels for packaging artworks
- Review materials and ensure compliance through Veeva
- Execute key regulatory actions to support business requirements
- Ensure adherence to current and new regulations
- Cascade relevant and new regulations from governing bodies
- Ensure database, reports, trackers are updated and provided on time
- Provide support to the Regulatory Affairs Director in terms of regulatory strategy and regulatory intelligence to ensure speed to market of products and compliance with regulatory guidelines.
- To provide regulatory training as required by the cross functional team.
- Create SOPs, process updates to support regulatory function.
- Active representation of the company with trade associations and ensure key company advocacies are pushed across.
Qualifications:
- B.S Pharmacy graduate and Licensed Pharmacist
- At least 3 to 5 years managerial experience in Regulatory Affairs