Regulatory Executive

Responsibilities Support development and execution of regulatory strategies aligned with Haw Par's strategic priorities. Prepare regulatory dossiers for new registrations, variations and renewal submissions to authorities in compliance with current regulatory requirements. Collaborate with cross-functional teams including Marketing, Quality, R&D and...

Responsibilities Support development and execution of regulatory strategies aligned with Haw Par’s strategic priorities. Prepare regulatory dossiers for new registrations, variations and renewal submissions to authorities in compliance with current regulatory requirements. Collaborate with cross-functional teams including Marketing, Quality, R&D and...

Job Description Support development and execution of regulatory strategies aligned with Haw Par’s strategic priorities. Prepare regulatory dossiers for new registrations, variations and renewal submissions to authorities in compliance with current regulatory requirements. Collaborate with cross-functional teams including Marketing, Quality, R&D and...

Support product registration activities, including the preparation of registration dossiers, performance evaluation study design, and coordination with CROs (Clinical Research Organizations). - Interface with global regulatory authorities such as the FDA, Health Sciences Authority (HSA), and Medical Device Authority (MDA). Track submission progress and...

**Our story began in 1971 when our founder at VKA, Master Flavorist Victor Koh, achieved what others couldn't - creating breakthrough flavors that set new industry benchmarks, including our pioneering tropical formulations that others had found impossible at the time. His principle remains at our core today: true innovation happens when talented people have...

Roles & Responsibilities Job Responsibilities: Support product registration activities, including the preparation of registration dossiers, performance evaluation study design, and coordination with CROs (Clinical Research Organizations). Act as the subject matter expert on medical device regulatory requirements, with a particular focus on FDA regulations....

**Accountabilities**: - **Quality Assurance**: Implement CPE standards within GE’s quality assurance systems as assigned. - **CPE Audits, Compliance and Reporting**: Coordinate CPE audits, reporting and ad-hoc requests as assigned. Execute the ERF registration process with CPE. Perform compliance monitoring of departments through activities assigned. -...

**Job description**: **Responsibilities** 1. Execute all regulatory activities including submission of new products or renewals until post-approval monitoring. 2. Understand the context of MDD/MDR, ISO 13485, AMDR, FDA 21 CFR Part 820, and other applicable regulations in the markets we served. 3. Compilation, review, coordination, submission, monitoring,...

Job Responsibilities Product registration: including preparation of registration dossier, design of performance evaluation study and manage execution and communication with CRO (clinical research organization). Be the subject matter expert on medical devices laws and regulations for product registration in company’s regions of interest. Interface the...

Job Responsibilities Product registration: including preparation of registration dossier, design of performance evaluation study and manage execution and communication with CRO (clinical research organization). Be the subject matter expert on medical devices laws and regulations for product registration in company's regions of interest. Interface the...