SEA Head of Regulatory Affairs - Singapore

We are seeking an experienced Regulatory Affairs/Regulatory Toxicology professional to support global regulatory compliance for our chemical manufacturing portfolio. · The position requires thorough knowledge of toxicological and ecotoxicological testing protocols and internation ...

The Regulatory &Product Safety Manager is responsible for ensuring that the company's chemical ingredients and formulations comply with all applicable global, regional, and local regulations across markets including Home & Personal Care... · ...

The Regulatory Affairs Pharmacist supports the company's regulatory activities to ensure compliance with Health Sciences Authority (HSA) requirements for medical devices. · ...

We seek individuals who thrive in collaborative environments, · sharing our love for craftsmanship,elegance,and integrity. · We're thrilled to announce · the opening for Regulatory Affairs Manager,to lead and coordinate · the company's regulatory affairs to ensure compliance in · ...

· About the job Regulatory Affairs Executive | Pharma MNC (7 months Contract) | Buona Vista · This position has responsibility for Regulatory Affairs within Malaysia, Singapore and Brunei. This includes: · Support regulatory affairs team on other regulatory affairs matters espec ...

We are looking for a Regulatory Affairs Specialist / Senior Speciallist. The successful candidate should have experience with products in Class C or D medical devices that are of high risk. · Regulatory application, Compliance · Maintain up-to-date documentation, · archival regu ...

Troubleshoot regulatory issues and maintain compliance for both B2B and B2C products across ASEAN markets. · Support other regulatory affairs activities as assigned by Japan Headquarters. · ...

As a Regulatory Affairs Specialist at Prosben Group Pte. Ltd., you will play a critical role in ensuring that the company's products, operations, and processes comply with applicable regulatory requirements across multiple markets. · ...

Alcotech Pte Ltd specializes in Infectious Disease Kits and Medical Device Regulatory Affairs. We support medical device manufacturers in navigating complex regulatory landscapes and securing market access across Singapore and Southeast Asia. · Role Overview · We are seeking a Re ...

· This position has responsibility for Regulatory Affairs within Malaysia, Singapore and Brunei. This includes: · Support regulatory affairs team on other regulatory affairs matters especially those which are required from personnel based in Singapore. · Ensure minimal supply d ...

Support market expansion and compliance in Asia Pacific region. · ...

The primary function of the Manager, Regulatory Affairs (RA) is to act as the representative of the regulatory affairs organization for all aspects related to the assigned therapeutic area. · CORE JOB RESPONSIBILITIES:Primary interface to and from the RA personnel in the affiliat ...

The company is looking for a Regulatory Affairs Specialist to handle regulatory applications and compliance for high-risk medical devices. · ...

Regulatory Affairs Specialist (Medical/ Therapeutic Products) · ...

Our client is looking for a Regulatory Affairs Specialist for medical device manufacturing company. · ...

Key requirements Good knowledge of ISO for medical device) · Good knowledge of product registration - in the EU (familiar with CE Mark, MDD, MDSAP, MDR) · Responsibilities:To act as Person Responsible and RA Manager to register, maintain and renew the product / establishment lice ...

We are partnering with a leading Japanese MNC in healthcare and medical solutions operating across multiple markets. · ...

This is a critical, regional compliance and project management role that acts as the key gatekeeper for product launches across multiple Asian markets. · ...

Challenging. Meaningful. Life-changing. · To be responsible for the regulatory activities in some ASEAN (Brunei, Malaysia, Singapore,) by providing technical information, · ...

The Regulatory Affairs Executive will be responsible for product registration including preparation of registration dossier and managing execution and communication with CRO. They will also be the subject matter expert on medical devices laws and regulations for product registrat ...

Job Summary · You will manage regulatory compliance and certification processes to ensure product integrity and market access. Collaborate with suppliers and internal teams to maintain accurate documentation and respond proactively to legislative changes affecting raw materials a ...