Lediga job som Medicinsk ingenjör

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

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

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

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

Därför är detta jobbet för dig På Knightec Group förstår vi att förbättrad livskvalitet för patienter genom att säkra medicintekniska produkter och läkemedel är av yttersta vikt. Genom att balansera kvalitet och regulatorisk efterlevnad under produkt- och produktionsutvecklingsprocessen, spelar du en avgörande roll i att introducera ny teknik och effektivare medicinteknisk utrustning och läkemedel till marknaden.

Din utveckling är viktig för oss. Din ambition och vilja styr riktningen, medan vi förser dig med verktygen och förutsättningarna för att lyckas. Genom mentorskap, kompetensdelningsforum, kunskapsutbyte och ett teamorienterat arbetssätt kommer du att kunna ta del av den samlade expertisen inom Knightec Group. Du blir en del av vårt nationella initiativ inom Medtech Compliance, där du bland annat får ta del av utbildningar och certifieringar.

Inom vårt affärsområde Compliance & Management stöttar vi en effektiv omställning till digitala, hållbara och säkra lösningar genom expertkunskap inom exempelvis kvalitet, säkerhet, hållbarhet och projektstyrning.

Ansvarsområden I rollen kommer du att arbeta i varierande och utvecklande uppdrag på bolag av olika karaktär där din expertis kommer tillrätta.

• Du kommer förbättra livskvaliteten för patienter genom säkra medicintekniska produkter och läkemedel

• Du strävar efter att hitta rätt balans mellan kvalitet och regulatorisk efterlevnad under produktutvecklingsprocessen

• Du strävar efter att hitta rätt balans mellan kvalitet och regulatorisk efterlevnad i en hårt reglerad produktionsmiljö som tex GMP

• Du vill vara en viktig del av att introducera ny teknik och mer effektiv medicinteknisk utrustning till marknaden

• Du vill använda hela din kompetens i varierande projekt, från start-ups till väletablerade internationella företag

• Du har expertis inom Design Control, teknisk dokumentation, Quality Assurance eller regulatoriska krav och vill ta stort ansvar i dina uppdrag

• Du värdesätter att arbeta i en miljö präglad av tillit, transparens och samarbete

Kvalifikationer Dina viktigaste egenskaper är din vilja att lära och dela din kunskap med andra. Då vår ambition är att hjälpa våra kunder ta nästa steg in i framtiden genom digitala verktyg, ser vi att du har intresse för ny teknik och digitalisering. Extra intressant är det om du har erfarenhet eller intresse för att arbeta med kvalitetssäkring av mjukvara eller uppkopplad utrustning.

Du har även:

• Ingenjörsexamen i bioteknik, medicinteknik, kemiteknik eller liknande

• Erfarenhet av att ha arbetat med produktutvecklingskvalitet inom den medicintekniska industrin, exempelvis Design Control, CE-märkning, Quality Assurance, Regulatory Affairs eller kvalitetsledningssystem

• Erfarenhet av att ha arbetat i reglerad produktionsmiljö, tex inom läkemedel.

• God kunskap om relevanta regulatoriska krav och standarder som exempelvis MDD/MDR, ISO 13485, ISO 14971, IEC 62304 och GMP

• Flytande kunskaper i svenska och engelska

En spännande resa med Knightec Group Semcon och Knightec har gått samman som Knightec Group. Tillsammans bildar vi Norra Europas ledande strategiska partner inom produkt- och digital tjänsteutveckling – hur häftigt är inte det?

Med en unik kombination av tvärfunktionell expertis och en holistisk förståelse för affärer hjälper vi våra kunder att förverkliga sina strategier – från idé till färdig lösning. På Knightec Group finns kompetensen, attityden och drivkraften som krävs för att anta de mest utmanande och innovativa projekten.

För våra medarbetare innebär detta fantastiska möjligheter att vara med och forma framtiden genom meningsfulla projekt i teknikens absoluta framkant. Här får du inte bara utvecklas och växa, utan också bli en del av något större.

Låter det som platsen för dig? Häng med på en spännande resa!

Praktisk information Detta är en tillsvidareanställning med en provanställning på sex månader, placerad på vårt kontor i Malmö, Ångbåtsbron 1. Resor i tjänsten kan förekomma till våra kunder. Startdatum är så snart som möjligt eller enligt överenskommelse.

Skicka in din ansökan så snart som möjligt, men senast 2026-11-01. Om du har några frågor om tjänsten är du välkommen att kontakta Talent Acquisition Specialist Oliver Rydberg. Observera att vi, på grund av GDPR, endast tar emot ansökningar via vår karriärsida.

Vi ser fram emot att höra från dig!

Därför är detta jobbet för dig På Knightec Group förstår vi att förbättrad livskvalitet för patienter genom att säkra medicintekniska produkter och läkemedel är av yttersta vikt. Genom att balansera kvalitet och regulatorisk efterlevnad under produkt- och produktionsutvecklingsprocessen, spelar du en avgörande roll i att introducera ny teknik och effektivare medicinteknisk utrustning och läkemedel till marknaden.

Din utveckling är viktig för oss. Din ambition och vilja styr riktningen, medan vi förser dig med verktygen och förutsättningarna för att lyckas. Genom mentorskap, kompetensdelningsforum, kunskapsutbyte och ett teamorienterat arbetssätt kommer du att kunna ta del av den samlade expertisen inom Knightec Group. Du blir en del av vårt nationella initiativ inom Medtech Compliance, där du bland annat får ta del av utbildningar och certifieringar.

Inom vårt affärsområde Compliance & Management stöttar vi en effektiv omställning till digitala, hållbara och säkra lösningar genom expertkunskap inom exempelvis kvalitet, säkerhet, hållbarhet och projektstyrning.

Ansvarsområden I rollen kommer du att arbeta i varierande och utvecklande uppdrag på bolag av olika karaktär där din expertis kommer tillrätta.

• Du kommer förbättra livskvaliteten för patienter genom säkra medicintekniska produkter och läkemedel

• Du strävar efter att hitta rätt balans mellan kvalitet och regulatorisk efterlevnad under produktutvecklingsprocessen

• Du strävar efter att hitta rätt balans mellan kvalitet och regulatorisk efterlevnad i en hårt reglerad produktionsmiljö som tex GMP

• Du vill vara en viktig del av att introducera ny teknik och mer effektiv medicinteknisk utrustning till marknaden

• Du vill använda hela din kompetens i varierande projekt, från start-ups till väletablerade internationella företag

• Du har expertis inom Design Control, teknisk dokumentation, Quality Assurance eller regulatoriska krav och vill ta stort ansvar i dina uppdrag

• Du värdesätter att arbeta i en miljö präglad av tillit, transparens och samarbete

Kvalifikationer Dina viktigaste egenskaper är din vilja att lära och dela din kunskap med andra. Då vår ambition är att hjälpa våra kunder ta nästa steg in i framtiden genom digitala verktyg, ser vi att du har intresse för ny teknik och digitalisering. Extra intressant är det om du har erfarenhet eller intresse för att arbeta med kvalitetssäkring av mjukvara eller uppkopplad utrustning.

Du har även:

• Ingenjörsexamen i bioteknik, medicinteknik, kemiteknik eller liknande

• Erfarenhet av att ha arbetat med produktutvecklingskvalitet inom den medicintekniska industrin, exempelvis Design Control, CE-märkning, Quality Assurance, Regulatory Affairs eller kvalitetsledningssystem

• Erfarenhet av att ha arbetat i reglerad produktionsmiljö, tex inom läkemedel.

• God kunskap om relevanta regulatoriska krav och standarder som exempelvis MDD/MDR, ISO 13485, ISO 14971, IEC 62304 och GMP

• Flytande kunskaper i svenska och engelska

En spännande resa med Knightec Group Semcon och Knightec har gått samman som Knightec Group. Tillsammans bildar vi Norra Europas ledande strategiska partner inom produkt- och digital tjänsteutveckling – hur häftigt är inte det?

Med en unik kombination av tvärfunktionell expertis och en holistisk förståelse för affärer hjälper vi våra kunder att förverkliga sina strategier – från idé till färdig lösning. På Knightec Group finns kompetensen, attityden och drivkraften som krävs för att anta de mest utmanande och innovativa projekten.

För våra medarbetare innebär detta fantastiska möjligheter att vara med och forma framtiden genom meningsfulla projekt i teknikens absoluta framkant. Här får du inte bara utvecklas och växa, utan också bli en del av något större.

Låter det som platsen för dig? Häng med på en spännande resa!

Praktisk information Detta är en tillsvidareanställning med en provanställning på sex månader, placerad på vårt kontor i Malmö, Ångbåtsbron 1. Resor i tjänsten kan förekomma till våra kunder. Startdatum är så snart som möjligt eller enligt överenskommelse.

Skicka in din ansökan så snart som möjligt, men senast 2026-11-01. Om du har några frågor om tjänsten är du välkommen att kontakta Talent Acquisition Specialist Oliver Rydberg. Observera att vi, på grund av GDPR, endast tar emot ansökningar via vår karriärsida.

Vi ser fram emot att höra från dig!