Senior Regulatory Affairs Specialist - Singapore

We are seeking a Regulatory Affairs Specialist with either experience working at the Health Sciences Authority (HSA) or prior experience in medical device regulatory affairs.The ideal candidate will manage medical device registrations, ensure compliance with regulations, and prov ...

We are hiring a General Affairs Specialist to support core corporate operations including visa administration, payroll support, financial, legal, and administrative document management. · Be responsible for the full process of employee visa application. · Assist in salary calcula ...

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

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 ...

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

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. · ...

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

The Academic Affairs Specialist supports the Academic Director in operational management and quality delivery of academic programmes. · ...

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

We are seeking a Quality and Regulatory Affairs (QRA) Specialist to support quality and regulatory activities for our products. · Degree in Engineering, Life Sciences, Pharmacy, or a related discipline. · Strong documentation, problem-solving, and communication skills. · ...

Senior Regulatory Affairs Specialist Job Description At Johnson & Johnson we believe health is everything Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented treated and cured where treatments are smarter and less invasive and s ...

We are partnered with a leading pharmaceutical company committed to innovative healthcare solutions across Asia. They are dedicated to enhancing patient well-being through rigorous regulatory compliance and strategic pharmaceutical development. · They are seeking an experienced R ...

We are seeking a Regional Regulatory Affairs Specialist to support and lead regulatory initiatives throughout Asia and the Middle East area (excluding China and Japan). The Specialist will manage more difficult regulatory activities autonomously, · Provide professional advice on ...

Subject matter expert in determining the current regulatory requirements and strategies for Merit Medical Singapore design control projects. · ...

This position involves assisting teachers with offline course activities such as inventory management and classroom support. · Offline Course Assistance: Inventory and manage offline activity materials. · Classroom Support: Assist in distributing printed teaching materials. Guide ...

This Senior Regulatory Affairs Specialist will ensure compliance with applicable regulatory requirements, corporate policies, and quality standards related to clinical trial supply chain operations. · Provide regulatory and quality guidance to internal stakeholders and clientsCoo ...

This is a Regulatory Affairs Specialist role for South-East Asia (SEA) markets. · ...

· As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. · Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. ...

As part of the Thermo Fisher Scientific team,you'll discover meaningful work that makes a positive impact on a global scale. · Ensure compliance with applicable regulatory requirements,c corporate policies,and quality standards related to clinical trial supply chain operations. · ...

Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better. · Responsible for the daily operations of regulatory affairs and assures regulatory submissions meet local and regional compliance requirements. · Generates and mana ...