Medical Device Regulatory Expertise

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...

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...

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...

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...

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 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...

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...

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...

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...

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...

In this role, you will be part of a talented team dedicated to developing and manufacturing innovative therapies. You will have the opportunity to work on complex projects, develop new skills, and contribute to our mission.The QC Manager will lead and inspire our Quality Control team to achieve analytical excellence and compliance. This involves overseeing...

Vipas AB is seeking a highly skilled Senior Embedded Software Developer for a long-term assignment with one of our clients in the MedTech industry. This role requires a strong understanding of software development for medical devices, including hardware connections and embedded system architecture.About UsAt Vipas AB, we strive to create tailored solutions...

As a Senior Embedded Software Developer at Vipas AB, you will be part of an innovative team driving the future of MedTech. Our client is seeking a skilled professional to develop and optimize embedded software solutions for medical devices.About the JobThis role requires a strong understanding of software development for medical devices, including hardware...

Join Our Team VIPAS AB as a Senior Embedded Software Developer (MedTech)Location: Malmö/Lund, SwedenJob type: Fulltime, OnsiteDo you have what it takes to thrive in the vibrant world of IT consulting? VIPAS AB, a burgeoning company, proudly invites you to embark on your next engaging project as our Senior Embedded Software Developer (MedTech).About...

Unlock Your Potential as a PathologistAre you ready to take your career to the next level? Dignus Medical/Kletor Sverige AB - Malmö offers an exciting opportunity for skilled pathologists to join our collaborative team. As a pathologist at our hospital, you will have the chance to work with cutting-edge technology and innovative approaches to patient...

Company OverviewDignus Medical/Kletor Sverige AB - Malmö is a leading University Hospital in Southern Sweden, seeking skilled pathologists to join a highly specialized and collaborative environment. We are committed to delivering the highest level of diagnostic precision through expertise and innovation.Job DescriptionAs a pathologist, you will work within...

Sök jobbet som QA-spezialist hos oss på PolyPeptide! Vi letar efter en erfaren QA-spezialist som vill vara med och forma verksamheten inom läkemedelsindustrin. Vår QA-avdelning på vår site i Limhamn består idag av ca 30 personer och arbetar nära vår produktion.ArbetsuppgifterQA specialist i kundprojektQA-representant i större...

Krav och kvalifikationerKandidatexamen inom området naturvetenskapMinst 5 års tidigare erfarenhet i rollen som QA i läkemedel- eller medical device industrinErfarenhet av GMPTidigare arbetat med avvikelsehantering, utredningar, riskbedömningar och batchgranskningMycket goda kunskaper i svenska och engelska i tal och skriftI din roll som Experienced QA...

Discover the Perfect Balance of Work and LifeSouthern Sweden offers a unique balance of city living and access to stunning natural beauty. Our region is known for its vibrant cultural life, excellent public services, and international atmosphere, making it an ideal place to settle for professionals and their families. As a pathologist at Dignus...

Are you a skilled Senior Embedded Software Developer looking for a new challenge? Do you have a strong understanding of software development for medical devices, including hardware connections and embedded system architecture?About the RoleWe are seeking a highly skilled professional to join our team as a Senior Embedded Software Developer. This role...