Regulatory Specialist for Medical Devices
3 weeks ago
Protect Public Health and Safety as a Regulatory Specialist
We are seeking highly motivated individuals with a strong desire to protect public health and safety to join our team as Regulatory Specialists in the medical devices industry.
- Key Responsibilities:
Screen and evaluate medical device pre/post-marketing applications to ensure they meet safety, quality, and performance requirements within target timelines.
Implement the medical device regulatory framework, including effective communication of the regulatory policy to industry and other stakeholders.
Respond to queries, feedback, and provide clarifications to educate industry stakeholders on regulatory requirements and enhance regulatory compliance.
Conduct periodic environmental scanning of the medical device market to prepare for appropriate regulatory controls for novel innovative medical devices.
- Requirements:
Possess knowledge and experience in related scientific disciplines, e.g., Biomedical Engineering, Biomedical Sciences, Medical Technology, Pharmacy, Public Health, or any related biomedical/clinical specialties.
Preferably 3-5 years of relevant experience in the medical technology industry, including medical software.
Past research experience in R&D, biological sciences, bioengineering, and biomedical areas will be an advantage but not essential.
Good communication and interpersonal skills.
Able to work independently, as well as in a team.
Able to work effectively with people from different backgrounds.
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