Lediga job som Medicinsk ingenjör

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

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

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

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

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

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

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

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

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

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