Medical Device Regulatory Specialist

Regulatory Affairs Career OpportunityWe have an exciting career opportunity for a Medical Device Regulatory Specialist to join our team. As a key member of our regulatory affairs team, you will be responsible for ensuring that our medical devices comply with all relevant regulatory requirements. This includes preparing and submitting product registration...

Job DescriptionWe are seeking a highly skilled Medical Device Regulatory Specialist to join our team. As a key member of our regulatory affairs department, you will be responsible for ensuring the compliance of our medical device products with regulatory agencies worldwide. This role requires strong expertise in regulatory affairs, including product...

Job SummaryRecruit Express seeks a skilled Regulatory Affairs Specialist for Medical Devices to join our team. As a key member of our regulatory affairs department, you will be responsible for ensuring the compliance of our medical device products with regulatory agencies worldwide. This role requires strong expertise in regulatory affairs, including product...

Job OverviewAs a Regulatory Affairs Specialist in Medical Devices, you will play a critical role in ensuring the company's products meet regulatory requirements. You will work closely with cross-functional teams to prepare and complete product registration tasks, including new product registration, registration amendments, and renewal...

Job Overview This position requires a very high level of autonomy to support Andaman Medical in achieving regulatory goals and objectives. The Regulatory Affairs Specialist is expected to drive best practices in office and administrative management within the organisation to maximize efficiency and growth. The main responsibility is to proactively support...

Job Overview This position requires a very high level of autonomy to support Andaman Medical in achieving regulatory goals and objectives. The Regulatory Affairs Specialist is expected to drive best practices in office and administrative management within the organisation to maximize efficiency and growth. The main responsibility is to proactively support...

Regulatory Affairs (Medical Device MNC / Office Hours)Permanent, Full-time opportunity in a Leading Medical Device MNC Great platform for Growth and Career Progression Work-life balance; 5 day work week As a Regulatory Affairs Specialist, you will be responsible for the registrations and renewals of products in the medical device space. Our client is a...

About the RoleThe Regulatory Affairs Specialist at Andaman Medical is responsible for driving regulatory compliance and ensuring that all medical devices meet the necessary regulatory standards. This role requires a strong understanding of regulatory requirements and the ability to communicate effectively with stakeholders.Main Tasks:Determine whether a...

Responsibilities and RequirementsThe Regulatory Affairs Specialist at Andaman Medical will be responsible for:Investigating whether a Health Product is a medical device requiring registration with MOH and determining its risk classification and route of submission.Preparing and submitting applications related to Initial, Renewal, Change Notification of...

Contract Regulatory Affairs Specialist (Medical Device) #HHL - Monthly Salary: Up to $5000- Location: Novena Key Responsibilities: Product Registration: Prepare and complete tasks for new product registration, registration amendments, and renewal registrations. Ensure product tests and samples meet safety and performance requirements of regulatory agencies...

About the JobThis is an exciting opportunity to join our team as a Medical Device Regulatory Compliance Expert. As a key member of our regulatory affairs team, you will be responsible for ensuring that our medical devices comply with all relevant regulatory requirements. Your primary focus will be on preparing and submitting product registration tasks,...

Roles & Responsibilities8-Month Contract Opportunity: Regulatory Affairs Specialist (Maternity Cover)Location: Novena Tentative Start Date: May/June 2025Salary: $5,000/monthKey Responsibilities: Review and approve documentation for product development and manufacturing processes. Prepare and submit comprehensive documentation packages to regulatory...

Roles & Responsibilities8-Month Contract Opportunity: Regulatory Affairs Specialist (Maternity Cover)Location: Novena Tentative Start Date: May/June 2025Salary: $5,000/monthKey Responsibilities: Review and approve documentation for product development and manufacturing processes. Prepare and submit comprehensive documentation packages to regulatory...

We are looking for a highly skilled Medical Device Quality Assurance Specialist to join our team at BSI.Job Description:As a Medical Device Auditor, you will be responsible for assessing the quality management systems of medical device manufacturers across APAC. Your role will involve traveling to these manufacturers' sites, conducting audits, and ensuring...

Job Description:The Contract Regulatory Affairs Specialist will be responsible for managing the regulatory aspects of medical devices at Recruit Express Pte Ltd.Responsibilities:Ensure compliance with regulatory requirements for medical devices, including product registration, labeling, and advertising.Liaise with internal stakeholders to ensure timely...

Regulatory Affairs RoleWe are seeking a skilled RA professional to join our team as a Medical Device Regulatory Specialist. In this role, you will be responsible for ensuring that our medical devices comply with all relevant regulatory requirements. This includes preparing and submitting product registration tasks, such as new product registration,...

Roles & ResponsibilitiesOverview of roleWe are looking for an energetic and organized individual to distribute orthotic devices (fracture braces) to our clients in a timely and efficient manner. The successful candidate will be responsible for ensuring that orthotic devices are delivered to the correct locations, handling inventory management, and providing...

Roles & ResponsibilitiesWe are seeking an experienced Medical Device Development Engineer with a strong background in the development and commercialization of medical devices. The ideal candidate will have over 5 years of relevant experience and a proven track record in innovative product design, prototyping, testing, and regulatory compliance. This role...

**Job Description:**We are seeking a skilled Regulatory Affairs Specialist to support the Asia Pacific Region in obtaining medical device pre-market regulatory approvals.This position will involve authoring regulatory submissions through third-party entities, staying vigilant of developing standards and regulations, and handling post-market agency reporting...

Roles & ResponsibilitiesOverview of roleWe are looking for an energetic and organized individual to distribute orthotic devices (fracture braces) to our clients in a timely and efficient manner. The successful candidate will be responsible for ensuring that orthotic devices are delivered to the correct locations, handling inventory management, and providing...