Medical Device Post Market Surveillance Specialist

Job Title: Regional Post Market Surveillance AnalystWe are seeking an experienced Regional Post Market Surveillance Analyst to join our team.The successful candidate will be responsible for performing post market surveillance analysis and supplier performance reporting, as well as maintaining quality management systems to meet regulatory requirements.Key...

Job Description: We are seeking a highly skilled and experienced Post Market Surveillance Manager to join our team. Main Responsibilities: To manage the post market surveillance activities in accordance with regulatory requirements, including FCA, Recall & FSCA, AE, and other QM related matters. To ensure the quality level of management and products...

Job Description:We are seeking a highly skilled and experienced Post Market Surveillance Manager to join our team.Main Responsibilities:To manage the post market surveillance activities in accordance with regulatory requirements, including FCA, Recall & FSCA, AE, and other QM related matters.To ensure the quality level of management and products is...

Job Description: We are seeking a highly skilled and experienced Post Market Surveillance Manager to join our team. Main Responsibilities: To manage the post market surveillance activities in accordance with regulatory requirements, including FCA, Recall & FSCA, AE, and other QM related matters. To ensure the quality level of management and products...

Job OverviewWe are seeking an experienced Regulatory Affairs Specialist to oversee medical device registrations, ensure compliance with regulations, and provide guidance on regulatory strategies. The ideal candidate will have experience working at the Health Sciences Authority (HSA) or prior experience in medical device regulatory affairs.Key...

Regulatory Affairs Specialist RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team. This individual will be responsible for managing medical device registrations, ensuring compliance with regulations, and providing guidance on regulatory strategy.Key Responsibilities:Prepare, review, and submit medical device registration...

Job Summary:This role is responsible for leading the development and implementation of quality management systems in the medical device industry. The Senior Quality Management Specialist will oversee post-market surveillance activities, manage computer system validation, and ensure compliance with regulatory standards.Key Responsibilities:Develop and...

Regulatory Medical Device ExpertWe are seeking a seasoned professional to lead our medical device registrations and compliance initiatives.Job Summary:The successful candidate will have expertise in managing medical device registrations, ensuring compliance with regulations, and providing strategic guidance.Key Responsibilities:Registration Management:...

Job OverviewWe are seeking a highly skilled regulatory professional to join our team.Key Responsibilities:Registration Management: Prepare, review, and submit medical device registration dossiers to relevant authorities. Monitor submissions in other ASEAN countries handled by local personnel.Regulatory Strategy:Advise on product classification, labelling,...

Job TitleWe are seeking a regulatory professional with expertise in medical device registrations and compliance.Manage registrations, ensure compliance with regulations, and provide guidance on strategic approaches.Key Responsibilities:Registration Management: Prepare, review, and submit medical device registration dossiers to relevant authorities. Monitor...