Regulatory Affairs Specialist

at  Magle Group

Magle Group is growing and we are looking Regulatory Affairs Specialist who is looking for a new challenge and who wants to be part of a small but dynamic regulatory team. Magle Group is supporting other Life Science Companies by providing CDMO services as well developing and manufacturing our own products with DSM technology. This role will focus on supporting our medical devices business and assure we comply with all regulatory standards and guidelines applicable in our active markets. The Regulatory Affairs Specialist plays a crucial role in the submission, registration, and lifecycle management of our medical device products.

QUALIFICATIONS:

• Bachelor’s degree in a scientific or related field; advanced degree preferred.
• Minimum of 2 years of experience in regulatory affairs, specifically with medical devices.
• Strong understanding of international regulatory guidelines and standards such as FDA, CE Marking, NBOG,ISO 13485, etc.
• Proven track record in preparing successful regulatory submissions.
• Excellent communication skills, both written and verbal, with the ability to interact effectively at all levels of the organization and with regulatory authorities.
• Highly organized and able to manage multiple projects simultaneously in a fast-paced environment.

• Prepare and submit regulatory documentation required for the approval and registration of new and existing products in various international markets.
• Be updated of regulatory procedures and changes in the regulatory climate to ensure compliance and advise the company on necessary adjustments.
• Legalization of registration documentation.
• Inform and educate the organisation on submission requirements and ensure necessary documents are provided.
• Maintain regulatory files and update regulatory authorizations, such as Investigational Device Exemptions (IDEs), 510(k) submissions, Canadian medical device licenses, and CE dossiers for the EU, as well as NRTL certifications.
• Maintenance of registrations , renewals, device listings, site registrations, supplements for changes, and annual reports.
• Respond to questions from regulatory authorities.
• Change control activities
• Assess device-related incidents and complaints for medical device reporting requirements. Compile and submit reportable events to relevant regulatory authorities in a timely manner. Handle recalls and field actions, if required.
• Review and create product labels and review promotional materials to ensure compliance with applicable regulations and technical standards.
• Assist in preparing clinical trial site ethics review board applications for investigational device trials. Prepare interim or final reports for trial site ethics boards as required.
• Other duties as assigned to support the regulatory team and ensure compliance with global regulatory requirements.