Regulatory Executive

A leading fintech firm in Singapore is seeking a mid-senior level Legal Counsel with approximately 5 years of PQE. The successful candidate will provide legal support across various fintech products while advising on regulatory requirements across multiple APAC jurisdictions. Requires strong knowledge in financial regulations and excellent communication...

Our client is a long-standing player in the healthcare sector, specializing in the distribution and promotion of pharmaceuticals, medical technologies, and wellness-related consumer goods across key regional markets. With a strong track record, they are widely regarded as a reliable and committed provider of health-related solutions. Guided by a...

**Summary**: Our client is a UK-based multinational company specializing in the creation of original fragrances and flavors. They are seeking a talented individual to join their team as a Regulatory Affairs Executive Primary **Responsibilities**: - Provide technical documentation to our customers in a timely manner. - Advise customers on products...

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...

**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. -...

**Responsibilities**: - Product registration: including preparation of registration dossier, design of performance evaluation study and manage execution and communication with CRO (clinical research organization). - Interface the communication with regulatory agencies, e.g. Health Science Authority, Medical Device Authority, Food and Drug Administration,...

**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,...

We are a global leader in manufacturing of medical devices and deliver solutions to improve lives through today’s technology and future innovation. Due to business needs, we are now seeking for multiple experienced Regulatory Affairs executives to be part of our Regulatory Affairs team for ongoing transformation projects due to expansion. **Regulatory...

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...