Global Regulatory Submissions Specialist

A leading technology company located in Singapore is seeking a Regulatory Affairs Specialist. This role involves the management of regulatory submissions, maintenance of documentation, and formatting of files using specialized software. Candidates should have 1 to 3 years of experience in the pharmaceutical or related industry, with a preference for those...

**Responsibility**: - Under the direction of senior staff, assist with the formatting and compilation of regulatory submissions through such tasks as entering information into Tables of Contents and creating tabs and submission labels. - Provide support assistance to senior staff in the upkeep of regulatory authority submission and correspondence logs (add...

The Regulatory Affairs Specialist (MD) is a member of the local Regulatory Affairs department, responsible for activities to support and actively contributing to the regulatory compliance of medical devices products under their responsibility. - The Regulatory Affairs Specialist (MD) will be a member of the local regulatory affairs department within Johnson...

A global regulatory consultancy in Singapore is seeking an experienced regulatory affairs specialist to manage submissions and ensure compliance with international standards. The ideal candidate has over 5 years of experience, is fluent in English, and will collaborate with cross-functional teams to integrate regulatory requirements throughout the product...

ICON is offering an opportunity to work within our dedicated, talented, supportive and friendly Global Regulatory Clinical Services (GRCS) team in clinical trials. The GRCS team has been in operation for 25+ years and comprises more than 400 regulatory professionals located in 48 countries, managing submissions in 60+ countries. As part of the GRCS team,...

As a Regulatory Affairs Specialist, you will develop and implement programs and processes and provide support to ensure that Agilent products are safe, legal, and meet or exceed customer expectations and quality in compliance with regulations, standards, company policies, and business objectives. You will perform activities which include: - Keeps abreast...

In this role, you will work with the team that ensures that Penumbra products are approved for use in countries around the world, thereby helping to bring our life-saving technologies to patients worldwide. You will be responsible for research, preparation, coordination, filing and maintenance of document package submissions for new products and changes to...

The company I’m representing is a leading consumer healthcare MNC with a good presence globally. They are looking for a Regulatory Affairs Specialist to help with their product registrations across the ASEAN region. This incumbent would have opportunities for career progression internally. **Responsibilities**: - To prepare and track overall regulatory...

[About JNPMEDI]In 2020, JNPMEDI was founded with the aim of enhancing Korea's globally recognized medical infrastructure by leveraging digital technologies such as blockchain and cloud computing through a cutting-edge medical data platform.We launched the clinical trial data management solution, Maven Clinical Cloud, which significantly contributed to the...

Resuscitation Job Summary: This position will report to the Senior Manager, Regulatory Affairs Regional Leader, JAPAC. The Primary role of the Specialist within the company is to assist Regulatory Affairs department to implement and administrate of organization activities to support and ensure regulatory compliance. At ZOLL, we're passionate about improving...