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Visar 3 av 3 lediga jobb för "Civilingenjör, medicinsk teknik" i Västra Götalands län
Rensa sökfilterProduction Support Engineer
When you can’t breathe, nothing else matters. That’s why a career at Breas Medical matters. Our mission is to improve the quality of life and care of respiratory patients around the world through a personal commitment to innovation, quality and customer focus. Are you our next Production Support Engineer? Are you an engineer who enjoys solving technical challenges and turning ideas into reliable manufacturing solutions? You may already have experience in production or manufacturing engineering, or you may be at the beginning of your career with a relevant technical education and an interest in medical technology. As a Production Support Engineer within R&D Sweden, you will play an important role in strengthening our production processes and supporting the introduction of new products and design changes. Working closely with Production, R&D, Quality and other cross-functional teams, you will help ensure that our products are manufactured safely, efficiently and in accordance with applicable quality and regulatory requirements. This is an opportunity to combine hands-on production support with continuous improvement, technical problem-solving and long-term development in a highly regulated and meaningful industry. The position is full-time, permanent and based on-site at Breas Medical’s headquarters in Mölnlycke, Sweden. Main responsibilities Provide technical support to Production and help resolve manufacturing and quality-related issues. Lead or support design transfers, new product introductions and the implementation of design changes. Develop and improve manufacturing processes, methods, tooling, equipment and work instructions. Plan, perform and document process, verification and validation activities. Analyse production performance and contribute to improvements in product quality, production yield, safety and cost efficiency. Support Lean initiatives and collaborate with cross-functional teams to achieve shared goals. About you You are a curious and solutions-oriented engineer who enjoys turning technical challenges into practical improvements. You work in a structured way, with attention to quality, safety and documentation. Collaboration comes naturally to you, and you are comfortable communicating with colleagues across different functions and areas of expertise. You have an open mindset, enjoy working close to production and are motivated by contributing to products and processes that make a meaningful difference. To be successful in this role, we believe you bring some of the following experience and skills: A university degree in production engineering, medical engineering, mechanical engineering, electronics or another relevant technical field. Experience or a strong interest in production, manufacturing processes or medical technology. An understanding of mechanics, electronics and software, and how these areas interact within a product. Experience or knowledge of Design for Manufacturing, design transfer, verification, validation, tooling or process development. A structured approach to problem-solving and technical documentation. Good spoken and written Swedish and English. Previous experience in production or manufacturing engineering is an advantage but not essential. We also welcome applications from recent graduates with a relevant educational background and an interest in developing within production engineering and medical technology. Knowledge of regulatory requirements and standards for medical devices, such as ISO 13485, MDR, IEC 60601-1 or FDA requirements, is considered an advantage. Be More with us Join Breas and become part of a company where your experience, ideas and ambition can make a meaningful difference. Apply today and explore what it means to Be More. Expected recruitment timeline Applications will be reviewed continuously. More about us Founded in 1991 in Gothenburg, Sweden, Breas Medical is a global specialist in home mechanical ventilation and airway clearance, with a growing portfolio of sleep therapy solutions. Our purpose is to help the world breathe better. We connect people throughout the respiratory journey by bringing together insights, innovation and care. Our solutions form a connected ecosystem that includes ventilation, airway clearance, interfaces, accessories, connectivity, services and clinical education, supporting patients, caregivers and healthcare professionals from therapy initiation to long-term care at home. Headquartered in Sweden, Breas has more than 300 employees and subsidiaries across Europe, Asia-Pacific and the Americas. Together with our network of specialised distributors, we serve customers in over 40 countries worldwide. Find out more: Breas Medical
Medtech Specialist
Job description MedTech Specialist - Consultant Opportunities Join Our Team at Randstad Life Sciences Randstad Life Sciences is looking for experienced and motivated MedTech professionals for future consultant assignments in the Gothenburg area. At Randstad Life Sciences, we are dedicated to helping you advance your career and achieve your goals. As a consultant with us, you will enjoy competitive compensation, valuable benefits, and the security of collective agreements. Your dedicated consultant manager will guide you throughout your journey, connecting you with diverse, rewarding assignments across leading life sciences organizations. Through our vast professional network, ongoing learning opportunities, and personalized support, we empower you to continuously grow and make an impact in your field. Please note that this is an open, proactive posting for future assignments. While scope and duration vary by client, typical engagements last approximately 6 months. We seek professionals across all levels of seniority to contribute to critical projects, ranging from R&D and laboratory work to quality assurance and clinical research. You will collaborate in cross-functional teams and with internal and external stakeholders. You are expected to follow strict and detailed regulatory standards and maintain precise documentation. You are a science-driven professional with a proactive mindset. You excel both independently and in team settings, demonstrating flexibility, curiosity, and a strong sense of responsibility. You are adept at building relationships and navigating complex stakeholder landscapes. At Randstad Life Sciences, we focus on specialized expertise as part of Randstad, a global leader in talent solutions dedicated to becoming the world's most equitable and focused talent organization. Based in the Netherlands, Randstad spans 39 markets with roughly 40,000 employees worldwide. By combining our expansive global reach with strong local connections, we deliver rewarding opportunities for academics and specialists. As your dedicated talent partner, we empower you to advance your career, acquire key skills, and thrive in a meaningful professional environment. At Randstad Life Science, we are committed to equity and diversity. We value individuality and welcome applications from all qualified candidates. Deadline: 2026-10-18, selection process and interviews will be ongoing, so please apply as soon as possible. For questions, please contact Klara Danielsson Please note: Applications sent via email will not be processed and will be deleted in accordance with GDPR compliance. Responsibilities Contribute to the development, testing, and quality assurance of medical devices and processes, adhering to strict regulatory standards and directives Maintain precise documentation in compliance with both company protocols and global regulatory requirements Collaborate effectively with internal and external stakeholders to drive project success Engage proactively in technical and cross-functional teams to build and maintain professional networks Qualifications MSc or engineering degree Medical Technology, Biotechnology, Chemistry, Pharmacy, or a closely related, relevant field 5-8 years documented professional experience within a medical technology company, specifically in the development, manufacture, or research of medical devices or services High level of attention to detail and accuracy Proficient in both English and Swedish (written and verbal) About the company Randstad På Randstad vet vi att alla människor har en plats på arbetsmarknaden. Med verksamhet över hela landet och inom alla kompetensområden hjälper vi människor att hitta ett jobb som känns bra, och där de får möjlighet att växa, utvecklas och uppnå sin fulla potential. Med närmare 600 000 anställda i 38 länder är Randstad världsledande inom HR-tjänster, med målsättningen att bli världens främsta och mest uppskattade partner på arbetsmarknaden. Genom att kombinera vår passion för människor med kraften i dagens teknologi hjälper vi människor och företag att uppnå deras fulla potential. Vi kallar det Human Forward.
Junior R&D ingenjör
Integration Diagnostics and its core products, Penguin RFA and Osseo100 measures dental implant stability to enable clinicians to decide when to load an implant. The technique has been developed in close cooperation with clinicians and experts in the field of dental implantology. Resonance Frequency Analysis (RFA) and the measurement unit Implant Stability Quotient (ISQ) were introduced into the dental implant industry in 2001 and are now established methods of measuring implant stability and osseointegration. In 2015, in response to the dental community’s need for an accessible ISQ measuring system, Integration Diagnostics Sweden AB (IDSAB) was founded. Sales have developed rapidly with clients today in + 70 countries globally. In 2018, Integration Diagnostics became part of the Japanese company Nakanishi Inc. Nakanishi Inc., is a world-leading company of professional dental instruments with the world’s top-share brand “NSK”. All its products are developed and manufactured in Japan and distributed to 135 countries around the globe. The NSK Group has 14 subsidiaries worldwide and has established a strong global sales network. We are currently looking for a, Junior R&D Engineer – Medtech As a Junior R&D Engineer, you will be part of a small and agile R&D team, working closely with the R&D Director, who is also the founder of the company. This role offers a unique opportunity to gain hands-on experience across the entire product lifecycle, from concept development and testing to technical documentation and production support. You will play an active role in maintaining and improving existing products while supporting the development of future innovations within IDSAB's medical device portfolio. Key responsibilities: Contribute to the maintenance, optimization, and continuous improvement of commercially available products. Support the development and refinement of R&D methodologies, development processes, verification activities, and testing procedures in collaboration with the R&D team. Manage existing technical documentation and prepare new technical documentation when required. Work cross-functionally with colleagues in R&D, Quality Assurance, Production, and Product Management. In this position, your daily work has a wide scope and is conducted in a dynamic, innovative international working environment. Qualifications • Master of Science in Engineering (M.Sc.) or Bachelor of Science in Engineering (B.Sc.) in Electronics, Engineering Physics, Medical Engineering, or a related field. • Good knowledge about medical device development • Fluent in Swedish and English Preferred Experience The following experience is considered an advantage: Hands-on experience from experimental work, laboratory environments, or workshop activities. Practical experience gained through master's thesis projects, personal side projects, student competitions, or involvement in student organizations focused on engineering, electronics, robotics, or product development. Experience in prototyping, CAD, testing, troubleshooting, or building technical systems. Previous experience within the medical device industry is highly valued. To succeed in this role, you are a user- and patient centric person with a strong drive to provide innovative products. You have a broad technical interest, and you can navigate in both hardware and software development. You will be part of an exciting and challenging journey shaping the company’s future and taking the business to new heights. In this role you will have a great opportunity to make an impact and improve the products and solutions we supply to the market, and you will have a big variation in activities. Application To apply, please send your CV to career@idsab.com By submitting your application, you also consent to us storing your personal data, including CV & cover letter. You can revoke the consent whenever you want.
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