Global Medical Device Compliance Manager

Job DescriptionWe are seeking a highly skilled Medical Device Compliance Specialist to join our team at Randstad - Göteborg. As a key member of our quality assurance department, you will play a crucial role in ensuring the compliance of our medical devices with regulatory requirements.Your primary responsibilities will include:Overseeing quality assurance...

We are seeking a highly experienced professional to lead our CBAS Regulatory team based in Gothenburg, Sweden. As Director of Regulatory Affairs, you will be responsible for developing and optimizing systems for tracking regulatory submissions and commitments, and leading the team in managing change controls and submission requirements.About the...

As a Medical Device Electronics Engineer at Techster Solutions, you will be part of a tight-knit team responsible for the hardware and embedded systems of our products. Your primary responsibilities will include developing and maintaining electronic components for new medical device projects, evaluating alternative design solutions, and creating technical...

As a Medical Device Sales Professional at Smith+Nephew, you will have the opportunity to make a meaningful impact on the lives of patients and healthcare professionals. Your primary focus will be on developing and executing strategies to drive sales growth and improve customer satisfaction in the Gothenburg region.Key responsibilities:Develop and implement...

XVIVO is a global leader in medical technology, dedicated to extending the life of organs for transplant patients. As a Regulatory Affairs Manager, you will play a key role in shaping the company's future and ensuring compliance with regulatory requirements.Key ResponsibilitiesThe key responsibilities of this position include:Managing regulatory affairs for...

Job Details:The Vitrolife Group is looking for an experienced Information Security Specialist to join our team. As a key member of our global IT organization, you will play a vital role in maintaining compliance, managing risks, and shaping the future of our secure and sustainable IT environment.About the Role:As our Information Security Specialist, you will...

Cochlear Limited is seeking a dynamic Director of Regulatory Affairs to lead our CBAS Regulatory team based in Gothenburg, Sweden. As Director of Regulatory Affairs, you will be responsible for shaping and executing global regulatory strategies, ensuring compliance and timely approvals for our acoustics products in regulated markets worldwide.About the...

Cochlear, a leading medical device company, seeks a seasoned professional to lead our regulatory affairs team. As Director of Regulatory Affairs, you will be responsible for shaping and executing global regulatory strategies, ensuring compliance and timely approvals for our acoustics products in regulated markets worldwide.About the RoleKey responsibilities...

About the CompanyRandstad - Göteborg is a dynamic and rapidly growing MedTech company committed to developing innovative medical devices that improve patient outcomes. We are looking for a highly motivated and experienced Mid-Senior Quality Assurance/Regulatory Affairs (QA/RA) Specialist to join our team.This position offers an exciting opportunity to...

Position Summary:We are seeking a proactive and skilled Information Security Specialist to strengthen our global IT organization and safeguard our information assets. This is a unique opportunity to play a vital role in maintaining compliance, managing risks, and shaping the future of our secure and sustainable IT environment.Key Responsibilities:-...

Position OverviewCochlear Limited seeks a seasoned professional in Regulatory Affairs to lead our CBAS Regulatory team. As the Director, you will shape global regulatory strategies, drive cross-functional partnerships, and ensure compliance with regulatory requirements.Key RequirementsEducation:Bachelor's degree in a related field.Master's degree...

Safeguard Global is seeking a highly skilled Global HR Manager to join our team. As a key member of the HR function, you will be responsible for providing guidance and support to employees across the globe. You will work closely with the leadership team to develop and implement HR strategies that align with the company's goals and objectives.About the...

Job Description:The Vitrolife Group is a global organization dedicated to reducing the barriers towards building a family. We leverage science and technology to make this dream a reality. As an Information Security Specialist, you will play a vital role in safeguarding our information assets and driving IT security excellence.About the Role:As our...

Contribute to Frictionless Flow in the Operating RoomIn Operation Room Solution (ORS) at Mölnlycke, we aim for frictionless flow in the operating room, with solutions designed for safety.The Technical Product Manager will be responsible for ensuring compliance with technical documentation standards for the designated product range.Analyze external...

Job Overview:At the Vitrolife Group, we aim to unlock the full potential of science and technology to reduce the barriers towards building a family. Our Information Security Specialist will play a crucial role in maintaining compliance, managing risks, and shaping the future of our secure and sustainable IT environment.About the Position:As an Information...

XVIVO is a global medical technology company dedicated to extending the life of organs for transplant patients.Company OverviewXVIVO is in a rapid growth phase, expanding geographically and developing new products. This position offers an opportunity to play a crucial role at the company.Job DescriptionWe are seeking a Regulatory Affairs Manager to join our...

Job DescriptionWe are seeking a highly skilled Service Leader – Application Compliance Management to join our team at Volvo Group. In this role, you will be responsible for coordinating and ensuring progress of Priority 0 initiatives and staying up-to-date in the application landscape.

QualificationsTo be successful in this role, you will need to have:A university degree in life science, engineering, or other relevant area.Comprehensive experience (+5 years) of both operational and strategic responsibility for QA and RA in the medical device industry.In-depth knowledge and experience in registering products in different markets...

XVIVO is a rapidly growing medical technology company that develops innovative solutions to extend the life of organs for transplant patients. As a Regulatory Affairs Manager, you will play a critical role in shaping the company's future.ResponsibilitiesThe key responsibilities of this position include:Ensuring compliance with regulatory requirements for...

Job DescriptionThe Global Chemical Governance Manager will lead the development and implementation of a comprehensive global chemical management governance framework that aligns with international chemical regulations and industry standards. This role is critical in ensuring compliance with regulatory standards, mitigating risks, and driving sustainability...