Coordinator, Regulatory Submissions

Location : WoodlandWorking Hours : 5 days per week (Mon to Fri: 8:00 AM – 5:30 PM)Willingness to commit to extended hours if requiredJob DescriptionPrepare and coordinate Development Control (DC) , Building Plan (BP) , and TOP/CSC submissions to BCA and URALiaise with QP (Architect) and consultants for regulatory approvals from SCDF, PUB, NEA, LTA, and...

Key Responsibilities Regulatory Submissions Management Prepare, review, and submit all required documentation to relevant authorities, ensuring accuracy and compliance with applicable regulations. Maintain a thorough understanding of local, regional, and national regulatory requirements Coordinate with internal teams, including design, engineering, and...

Roles & Responsibilities Key Responsibilities Regulatory Submissions Management Prepare, review, and submit all required documentation to relevant authorities, ensuring accuracy and compliance with applicable regulations. Maintain a thorough understanding of local, regional, and national regulatory requirements Coordinate with internal teams, including...

Job Summary: We are currently seeking a full-time, office-based Study Start up Submissions Coordinator to join our Clinical Operations team in the Singapore office. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company’s success. If you are interested in an exciting career where you can use your...

**Responsibilities** - Management of permitting schedule - Executing permitting submission to authorities from start to TOP - Management of drawings and information between engineering and permitting team **Qualification** - Min. Diploma in Architecture / Civil Engineering - Must have local architectural / civil engineering permitting coordination...

Company Description Work with Us. Change the World.At AECOM, we're delivering a better world. Whether improving your commute, keeping the lights on, providing access to clean water, or transforming skylines, our work helps people and communities thrive. We are the world's trusted infrastructure consulting firm, partnering with clients to solve the world's...

Job Summary We are currently seeking a full-time Study Start Up Submissions Manager to join our Clinical Operations team in Singapore. Responsibilities Efficiently manage and successfully execute all aspects of global start-up; Perform quality checks on submission documents and site essential documents; Prepare and approve informed consent forms; Review...

Roles & Responsibilities Location : Woodland Working Hours : 5 days per week (Mon to Fri: 8:00 AM – 5:30 PM) Willingness to commit to extended hours if required Job Description Prepare and coordinate Development Control (DC) , Building Plan (BP) , and TOP/CSC submissions to BCA and URA Liaise with QP (Architect) and consultants for regulatory approvals...

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...

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....