Medical Device Maintenance Expert

We are Magle Group, a value-driven organization that has an interesting journey ahead. We are looking for a talented Regulatory Affairs Specialist to support our medical devices business and ensure compliance with all regulatory standards and guidelines applicable in our active markets.This role will be responsible for preparing and submitting regulatory...

Are you a motivated and detail-oriented individual with expertise in medical device packaging? We are looking for a Medical Device Packaging Specialist to join our team at Capgemini Engineering. As a key member of our packaging development team, you will be responsible for developing and implementing packaging solutions that meet stringent standards for...

As a key member of our regulatory team, you will be responsible for preparing and submitting regulatory documentation required for the approval and registration of new and existing products in various international markets.You will stay updated on regulatory procedures and changes in the regulatory climate to ensure compliance and advise the company on...

About the PositionAs a Medical Technology Support Engineer, you will play a critical role in ensuring the smooth operation of our systems and equipment. You will be responsible for installing, maintaining, and troubleshooting our products, as well as providing expert technical assistance to our customers.Your primary goal will be to deliver exceptional...

Job Title: Quality Engineer – Medical Device (Drug Development)Overview:We are seeking a highly skilled Quality Engineer to join our team in Sweden. As a Quality Engineer, you will play a crucial role in ensuring compliance with international quality standards in the development of medical devices for drug delivery systems.Key Responsibilities:Ensure...

Person Specification:We are seeking a highly experienced Production Process Expert to join our production team at Nordberg Medical AB. The ideal candidate will have around 5-8 years of experience in process engineering within the pharmaceutical or medical device industry, with a strong understanding of GMP, ISO 13485, FDA 21 CFR Part 820, and other...

Job Overview:We are seeking a skilled Regulatory Affairs Specialist to join our regulatory team. In this role, you will be responsible for ensuring compliance with international regulatory standards and guidelines applicable in our active markets.Your key responsibilities will include:Preparing and submitting regulatory documentation required for the...

Key Responsibilities:The Regulatory Affairs Specialist will be responsible for ensuring compliance with international regulatory standards and guidelines applicable in our active markets. The key responsibilities of this position include:Preparing and submitting regulatory documentation required for the approval and registration of new and existing products...

We are looking for an experienced Medical Device Manager to join our team in Lund, Sweden. As a key member of our cross-functional team, you'll be responsible for driving market and new product development strategies for our cutting-edge med tech product.Your responsibilities will include developing and executing the 5-year business strategy, driving new...

Magle Group is a dynamic company located in Malmö that supports Life Science Companies by providing CDMO services and developing and manufacturing our own products with DSM technology.We are looking for a Regulatory Affairs Specialist who will focus on supporting our medical devices business and ensuring compliance with all regulatory standards and...

Magle Chemoswed AB is expanding its regulatory team and seeking a skilled Regulatory Affairs Specialist to support our medical devices business. As a key member of the team, you will be responsible for ensuring compliance with regulatory standards and guidelines applicable in our active markets.Responsibilities:Develop and implement regulatory strategies to...

About the Role:The successful candidate will have a strong background in quality engineering and be able to work closely with R&D, manufacturing, and regulatory teams to ensure quality and drive continuous improvement throughout the product development lifecycle.Responsibilities:Comply with FDA, ISO 13485, and other applicable standards.Risk assessment and...

In this role, you will perform other duties as assigned to support the regulatory team and ensure compliance with global regulatory requirements. This may include reviewing and creating product labels and promotional materials to ensure compliance with applicable regulations and technical standards.You will also conduct change control activities, assess...

Role Overview:We're looking for a seasoned Quality Engineer to oversee the quality aspects of our medical device projects.Key Tasks:Oversee quality system implementation and maintenance.Develop and execute quality plans.Conduct regular audits to ensure compliance.Collaborate with cross-functional teams to address quality concerns.Build and maintain strong...

We are seeking a Device Installation Professional to join our technical customer support team. In this role, you will be responsible for installing new devices and software in hospitals, as well as performing maintenance and inspections of systems and devices.You will work independently from your home office to deliver results and ensure that customer...

Role Overview:We are seeking a highly motivated and experienced Medical Education Lead to join our team in Europe. This is an exciting opportunity to play a key role in planning and executing Healthcare Professionals' (HCPs) course trainings, product trainings, workshops, etc. – in alignment with our strategic goals and in partnership with stakeholders...

About the Role:We are seeking a highly experienced Manufacturing Operations Specialist to join our production team at Nordberg Medical AB. This role involves leading and supporting the development, optimization, and validation of manufacturing processes for our implantable Class III medical devices.You will work closely with cross-functional teams, including...

Job Description:We are seeking a highly skilled Senior Production Process Engineer to join our team at Nordberg Medical AB. As a key member of our production team, you will be responsible for leading and supporting the development, optimization, and validation of manufacturing processes for our implantable Class III medical devices.This role involves...

Magle Group is a dynamic and innovative company that provides CDMO services and develops and manufactures products with DSM technology. We are seeking a talented Regulatory Affairs Specialist to join our team and support our medical devices business.This role will involve preparing and submitting regulatory documentation required for approval and...

At Magle Group, we believe in making an impact by improving lives for patients worldwide. We are seeking a highly skilled Regulatory Affairs Specialist to join our team and support our medical devices business.This role will involve preparing and submitting regulatory documentation required for approval and registration in various international markets, as...