Medical Device Compliance Specialist

Job DescriptionWe are looking for an experienced Medical Device Installation Specialist to join our team. As a key member of our technical customer support team, you will be responsible for installing new medical devices and software in hospitals and ensuring their proper functioning.Main Responsibilities:Install new medical devices and software in...

Job DescriptionWe are seeking a skilled Medical Device Project Lead to join our team at Oticon Medical. As a key member of our Operations team, you will drive operational projects and improvements for in-market and new products. Your expertise in project management, manufacturing, and supply chain will be essential in ensuring timely and high-quality...

Mid-Senior Quality Assurance and Regulatory Affairs Specialist OverviewA dynamic and experienced professional is sought to lead quality assurance processes and ensure regulatory compliance for medical devices.This individual will collaborate with cross-functional teams to achieve successful product commercialization and maintain ongoing regulatory...

Key Responsibilities:Regulatory Strategy and Planning: Support project teams with regulatory advice, define documentation needs, and develop regulatory strategies to support business plans.Regulatory Submissions and Related Activities: Prepare submissions for product approvals, adapt technical dossiers, and coordinate support for regional subsidiaries and...

Leading the Way in Medical Device DevelopmentJob OverviewAs a Digital Transformation Leader in Medical Devices, you will lead teams developing innovative medical devices. Your primary responsibility will be to ensure products meet customer needs and regulatory standards.Key Responsibilities:Develop and implement project plans to meet customer...

Randstad seeks a talented Medical Device QA and RA Manager to oversee the quality assurance process and ensure compliance with industry regulations.This role will involve working closely with internal stakeholders to develop and implement quality systems and regulatory strategies.Main Responsibilities:Oversee the entire quality assurance process from design...

Key Responsibilities of a Mid-Senior Quality Assurance and Regulatory Affairs SpecialistThe ideal candidate will play a pivotal role in overseeing quality assurance processes, ensuring seamless compliance with regulatory requirements for medical devices.This professional will work closely with cross-functional teams to drive the successful commercialization...

Transforming Patient Care through Innovative ProjectsYour Role as a Senior Project ManagerAt Alten Sverige AB, you will lead the development of medical devices that enhance patient safety. Your primary responsibility will be to ensure products meet customer needs and regulatory standards.Key Responsibilities:Develop and implement project plans to meet...

Project Manager within MedTechWe are seeking a skilled Project Manager to lead and develop projects within Medical devices in Gothenburg.About the RoleIn this key position, you will be responsible for overseeing and developing projects within medical device development.Your primary focus will be on ensuring that products meet customer inputs, product...

Job Description">Mölnlycke Health Care is seeking a highly skilled Product Developer to join our innovative team at our new headquarters in GoCo Health Innovation City. As a key member of our Gloves R&D team, you will be responsible for developing and implementing new products to meet customer needs and growth goals.">Responsibilities">Develop and implement...

Job DescriptionTechster Solutions is currently undergoing a period of exciting growth and development, seeking highly skilled professionals to join its team.You can expect a dynamic work environment with varied tasks and opportunities for professional growth and development.As a knowledge-driven company, we value the sharing of expertise and collaboration...

Key AccountabilitiesYou will be accountable for delivering high-quality project outcomes, meeting customer expectations, and adhering to regulatory standards. In addition, you will contribute to the development of ALTEN's capabilities in medical device development and design control processes.

Job Title: Regulatory Affairs SpecialistXVIVO is a global medical technology company dedicated to extending the life of organs. We are in a rapid growth phase, expanding geographically and developing new products and supporting processes.Key Responsibilities:Manage vigilance/MDR reporting for markets where XVIVO has a presence.Lead regulatory affairs for...

We are seeking a highly motivated and experienced Mid-Senior Quality Assurance/Regulatory Affairs (QA/RA) Specialist to join our dynamic and rapidly growing MedTech company.This role offers an exciting opportunity to contribute to the development of cutting-edge products while ensuring compliance with the highest industry standards in medical devices.Main...

Product Development OpportunitiesWe are looking for a highly motivated and experienced Product Developer to join our innovative team at Molnlycke Health Care. As a key member of our R&D team, you will play a crucial role in developing innovative medical products that meet the evolving needs of healthcare professionals and patients worldwide.About the...

Job ResponsibilitiesThe successful Supply Chain Optimization Specialist will be responsible for driving operational projects and improvements for in-market and new products. This includes leading operations-related activities in product development projects and acting as the link between R&D and external production facilities. Additionally, you will drive...

Role Summary:As the Director of Regulatory Affairs, you will play a pivotal role in leading our Regulatory team in Gothenburg and ensuring compliance and timely approvals for acoustics products worldwide. This is an excellent opportunity to work with a global leader in implantable hearing solutions and make a significant impact on a global scale.The ideal...

About ALTENALTEN is a leading technology consulting company with over 57,000 employees worldwide.Our engineers work on complex projects across various industries, including Life Sciences. In Sweden, we have 9 offices and approximately 1,300 employees committed to delivering high-quality services.We strive to improve people's health by leading teams and...

Randstad is currently looking for a highly skilled Senior Regulatory Affairs Specialist to support the growth and development of our dynamic team.This position will focus on ensuring that all products meet the highest industry standards and comply with relevant regulations.Main Responsibilities:Maintain oversight of quality assurance processes and regulatory...

At the Vitrolife Group, we strive to create a safe and secure environment for our customers and employees. As an Information Security Specialist, you will play a critical role in protecting our assets and maintaining compliance with regulatory requirements.About the RoleCompliance Management: Monitor and report on compliance with internal and external...