Regulatory Affairs Specialist

Magle Group is growing and we are looking Regulatory Affairs Specialist who is looking for a new challenge and who wants to be part of a small but dynamic regulatory team. Magle Group is supporting other Life Science Companies by providing CDMO services as well developing and manufacturing our own products with DSM technology. This role will focus on...

Job Description:Magle Chemoswed is a leading provider of Contract Development and Manufacturing Organization (CDMO) services to the Life Science industry. We are seeking a highly skilled Regulatory Affairs Specialist to join our dynamic regulatory team.In this role, you will be responsible for ensuring compliance with international regulatory standards 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...

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...

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...

Job DescriptionWe are seeking a highly skilled Senior Regulator Affairs Consultant to join our team in Malmö.In this role, you will work closely with major pharmaceutical clients to deliver patient-focused, compliant, and efficient solutions. Your expertise will be crucial in navigating complex CMC regulatory requirements, ensuring that pharmaceutical...

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...

Magle Group is a dynamic and growing company in the Life Science industry, providing CDMO services and developing products with DSM technology. As a Regulatory Affairs Specialist, you will play a crucial role in ensuring compliance with regulatory standards and guidelines applicable in our active markets.Key Responsibilities:Prepare and submit regulatory...

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...

Magle Group is a dynamic and innovative company that provides CDMO services and develops and manufactures products with DSM technology. We are seeking a highly skilled Regulatory Affairs Specialist to join our small but dynamic regulatory team. This role will focus on supporting our medical devices business and ensuring compliance with all regulatory...

Job DescriptionAs a Medical Affairs Specialist for the Nordic region, you will be responsible for developing and executing Medical Affairs strategy and plans for the region. This includes providing medical/scientific strategic and operational expertise and leadership for all Medical Affairs activities.ResponsibilitiesDevelop and maintain up-to-date knowledge...

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...

Job OverviewCapgemini Engineering seeks a talented Senior Regulator Affairs Consultant to join our team in Malmö. In this role, you will have the opportunity to work with major pharmaceutical clients, driving business growth and delivering high-quality solutions.You will be responsible for developing and implementing regulatory strategies, ensuring...

Responsibilities:As a Regulatory Affairs Specialist, 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 approval and registration of new and existing products in...

About the RoleThis position is ideal for a professional with exceptional skills in coordinating and advising on pharmaceutical regulatory affairs. As a Senior Regulator Affairs Consultant, you will be working with diverse clients, providing strategic guidance and support to achieve their quality and regulatory objectives.The role involves collaborating with...

About Our CompanySever Pharma Solutions is a leading manufacturer of pharmaceuticals and combination products that meets or exceeds regulatory requirements.We strive for excellence in everything we do, from research and development to production and quality control.Learn more about us on our website.Job SummaryWe are seeking a Regulatory Compliance...

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...

The successful candidate will have a strong understanding of international regulatory guidelines and standards such as FDA, CE Marking, NBOG, ISO 13485, MDR, etc., and will be able to apply this knowledge to prepare successful regulatory submissions.You will work closely with cross-functional teams to ensure compliance with global regulatory requirements and...

Senior Regulator Affairs Consultant Job SummaryThis is an exciting opportunity to join Capgemini Engineering as a Senior Regulator Affairs Consultant in Malmö. In this role, you will have the chance to work with diverse clients, providing strategic guidance and support to achieve their quality and regulatory objectives.You will be responsible for developing...

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...