Medical Device Compliance Specialist

Job Title: Clinical Regulatory SpecialistThe role of a Clinical Regulatory Specialist is pivotal in the development of innovative medical devices. Key responsibilities include supporting design development, verification, clinical trials, validation, and regulatory approval.Key ResponsibilitiesCoordinate global clinical trial execution, including site...

Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to fill a key role in our organization. The successful candidate will be responsible for post-market activities for medical devices, supporting departmental regulatory processes and procedures, and ensuring compliance with global regulations.Key...

Medical Device Manufacturing SpecialistA Medical Device Manufacturing Specialist is responsible for developing, implementing, and optimizing high-performance manufacturing processes for medical devices.Main Responsibilities:Design and develop advanced manufacturing processes for medical devicesCollaborate with cross-functional teams to support new product...

**Regulatory Support Administrator Role Overview**Job Description:This role is responsible for providing administrative and regulatory support to the Medical Devices department, ensuring compliance with EU and national medical device legislation.The Regulatory Support Administrator will be involved in case handling, data management, communication, and...

Job OverviewThis role is responsible for leading the technical regulatory compliance of medical devices and drug-device combination products. The successful candidate will have a strong understanding of FDA, EU, and ISO standards, regulations, and guidance related to design control and regulatory compliance.Key ResponsibilitiesMaintain awareness of current...

Job SummaryThe role of Regulatory Affairs Specialist is crucial for the post-market activities of medical devices, supporting departmental regulatory processes and procedures, strategies, authoring, reviewing, and supporting global registrations.Main Responsibilities:Support regulatory strategies for OUS medical devices and combination products, ensuring...

Job TitleWe are seeking a highly skilled Medical Device Assurance Specialist to play a crucial role in ensuring the design and development of medical devices comply with regulatory requirements.Main Responsibilities:Support and provide guidance for device development programs through the design and development lifecycle.Ensure compliance to design control...

Regulatory Affairs Expert OpportunityWe are seeking a highly skilled Regulatory Affairs Specialist to play an active role in developing the regulatory strategy for medical device companies.The ideal candidate will have extensive knowledge of quality management systems, design controls per ISO 13485, and current International and European...

Device Regulatory Specialist - A Role in Pharmaceutical and Medical Device DevelopmentJob DescriptionWe are seeking a skilled Device Regulatory Specialist to join our team in the design, development, and commercialization of medical device technology solutions. Our organization is focused on delivering innovative healthcare solutions for patients...

Job OverviewWe are seeking a skilled medical device technical specialist to lead the implementation of a Quality Management System (QMS) aligned to ISO 13485.The ideal candidate will have experience in medical device roles and a proven track record of designing and implementing quality management systems.A strong understanding of ISO 13485 and related...