Lediga job som Forskningsingenjör

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn.

In this role, you will join the Non-Clinical Development team in Lund and contribute to the development of innovative medicines in a dynamic and collaborative environment. You will play a central role in the toxicological strategy for Camurus' products, working closely with colleagues across multiple disciplines as well as external partners.

We are looking for an experienced Senior Research Scientist, Toxicology to join our Non-Clinical Development team.

This is a strategic and cross-functional role where you will be responsible for developing non-clinical plans, designing toxicology programs and coordinating outsourced non-GLP and GLP toxicology studies performed by Contract Research Organizations (CROs). Acting as Sponsor Monitor, you will oversee study design, study conduct, data review and final reports, ensuring scientific quality, regulatory compliance and timely delivery. You will also contribute to regulatory submissions by preparing and reviewing non-clinical documentation and representing Non-Clinical Development in product development teams.

Main responsibility Among others, your responsibilities will include:

· Develop toxicology strategies and non-clinical development plans.

· Design and monitor outsourced GLP studies.

· Select, manage and collaborate with international CRO partners.

· Prepare and review toxicology reports and regulatory documentation.

· Represent Non-Clinical Development in cross-functional development teams.

· Ensure compliance with GLP and international regulatory requirements (ICH, FDA, EMA and OECD).

Candidate profile You hold a PhD or MSc in Toxicology, Pharmacology or another relevant Life Science discipline.

You have several years of experience from non-clinical drug development within the pharmaceutical, biotechnology or CRO industry. Experience of planning, monitoring or conducting GLP toxicology studies is essential, and you are familiar with outsourced development and regulatory requirements. Experience as a Sponsor Monitor or Study Director is highly valued.

You are an experienced scientific writer with solid knowledge of regulatory documentation. You are able to author the full range of non-clinical documentation, e.g non-clinical overviews and summaries for regulatory submissions, and the non-clinical parts of the Investigator’s Brochure (IB). Experience of regulatory submissions is an advantage.

As a person, you are collaborative, structured and proactive. You enjoy coordinating complex projects, building strong relationships and working in a cross-functional, international and deadline-driven environment. Fluency in spoken and written English is required.

Camurus offers

This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other.

You will have a broad area of responsibility and drive multiple non-clinical programs, working closely with leading international CROs and cross-functional development teams. With your toxicology background you will have a crucial role in R&D related activities.

Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment.

Information and application

For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/.

We are looking forward to seeing your application!

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn.

In this role, you will join the Non-Clinical Development team in Lund and contribute to the development of innovative medicines in a dynamic and collaborative environment. You will play a central role in the toxicological strategy for Camurus' products, working closely with colleagues across multiple disciplines as well as external partners.

We are looking for an experienced Senior Research Scientist, Toxicology to join our Non-Clinical Development team.

This is a strategic and cross-functional role where you will be responsible for developing non-clinical plans, designing toxicology programs and coordinating outsourced non-GLP and GLP toxicology studies performed by Contract Research Organizations (CROs). Acting as Sponsor Monitor, you will oversee study design, study conduct, data review and final reports, ensuring scientific quality, regulatory compliance and timely delivery. You will also contribute to regulatory submissions by preparing and reviewing non-clinical documentation and representing Non-Clinical Development in product development teams.

Main responsibility Among others, your responsibilities will include:

· Develop toxicology strategies and non-clinical development plans.

· Design and monitor outsourced GLP studies.

· Select, manage and collaborate with international CRO partners.

· Prepare and review toxicology reports and regulatory documentation.

· Represent Non-Clinical Development in cross-functional development teams.

· Ensure compliance with GLP and international regulatory requirements (ICH, FDA, EMA and OECD).

Candidate profile You hold a PhD or MSc in Toxicology, Pharmacology or another relevant Life Science discipline.

You have several years of experience from non-clinical drug development within the pharmaceutical, biotechnology or CRO industry. Experience of planning, monitoring or conducting GLP toxicology studies is essential, and you are familiar with outsourced development and regulatory requirements. Experience as a Sponsor Monitor or Study Director is highly valued.

You are an experienced scientific writer with solid knowledge of regulatory documentation. You are able to author the full range of non-clinical documentation, e.g non-clinical overviews and summaries for regulatory submissions, and the non-clinical parts of the Investigator’s Brochure (IB). Experience of regulatory submissions is an advantage.

As a person, you are collaborative, structured and proactive. You enjoy coordinating complex projects, building strong relationships and working in a cross-functional, international and deadline-driven environment. Fluency in spoken and written English is required.

Camurus offers

This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other.

You will have a broad area of responsibility and drive multiple non-clinical programs, working closely with leading international CROs and cross-functional development teams. With your toxicology background you will have a crucial role in R&D related activities.

Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment.

Information and application

For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/.

We are looking forward to seeing your application!

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn.

In this role, you will join the Non-Clinical Development team in Lund and contribute to the development of innovative medicines in a dynamic and collaborative environment. You will play a central role in the toxicological strategy for Camurus' products, working closely with colleagues across multiple disciplines as well as external partners.

We are looking for an experienced Senior Research Scientist, Toxicology to join our Non-Clinical Development team.

This is a strategic and cross-functional role where you will be responsible for developing non-clinical plans, designing toxicology programs and coordinating outsourced non-GLP and GLP toxicology studies performed by Contract Research Organizations (CROs). Acting as Sponsor Monitor, you will oversee study design, study conduct, data review and final reports, ensuring scientific quality, regulatory compliance and timely delivery. You will also contribute to regulatory submissions by preparing and reviewing non-clinical documentation and representing Non-Clinical Development in product development teams.

Main responsibility Among others, your responsibilities will include:

· Develop toxicology strategies and non-clinical development plans.

· Design and monitor outsourced GLP studies.

· Select, manage and collaborate with international CRO partners.

· Prepare and review toxicology reports and regulatory documentation.

· Represent Non-Clinical Development in cross-functional development teams.

· Ensure compliance with GLP and international regulatory requirements (ICH, FDA, EMA and OECD).

Candidate profile You hold a PhD or MSc in Toxicology, Pharmacology or another relevant Life Science discipline.

You have several years of experience from non-clinical drug development within the pharmaceutical, biotechnology or CRO industry. Experience of planning, monitoring or conducting GLP toxicology studies is essential, and you are familiar with outsourced development and regulatory requirements. Experience as a Sponsor Monitor or Study Director is highly valued.

You are an experienced scientific writer with solid knowledge of regulatory documentation. You are able to author the full range of non-clinical documentation, e.g non-clinical overviews and summaries for regulatory submissions, and the non-clinical parts of the Investigator’s Brochure (IB). Experience of regulatory submissions is an advantage.

As a person, you are collaborative, structured and proactive. You enjoy coordinating complex projects, building strong relationships and working in a cross-functional, international and deadline-driven environment. Fluency in spoken and written English is required.

Camurus offers

This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other.

You will have a broad area of responsibility and drive multiple non-clinical programs, working closely with leading international CROs and cross-functional development teams. With your toxicology background you will have a crucial role in R&D related activities.

Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment.

Information and application

For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/.

We are looking forward to seeing your application!

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn.

In this role, you will join the Non-Clinical Development team in Lund and contribute to the development of innovative medicines in a dynamic and collaborative environment. You will play a central role in the toxicological strategy for Camurus' products, working closely with colleagues across multiple disciplines as well as external partners.

We are looking for an experienced Senior Research Scientist, Toxicology to join our Non-Clinical Development team.

This is a strategic and cross-functional role where you will be responsible for developing non-clinical plans, designing toxicology programs and coordinating outsourced non-GLP and GLP toxicology studies performed by Contract Research Organizations (CROs). Acting as Sponsor Monitor, you will oversee study design, study conduct, data review and final reports, ensuring scientific quality, regulatory compliance and timely delivery. You will also contribute to regulatory submissions by preparing and reviewing non-clinical documentation and representing Non-Clinical Development in product development teams.

Main responsibility Among others, your responsibilities will include:

· Develop toxicology strategies and non-clinical development plans.

· Design and monitor outsourced GLP studies.

· Select, manage and collaborate with international CRO partners.

· Prepare and review toxicology reports and regulatory documentation.

· Represent Non-Clinical Development in cross-functional development teams.

· Ensure compliance with GLP and international regulatory requirements (ICH, FDA, EMA and OECD).

Candidate profile You hold a PhD or MSc in Toxicology, Pharmacology or another relevant Life Science discipline.

You have several years of experience from non-clinical drug development within the pharmaceutical, biotechnology or CRO industry. Experience of planning, monitoring or conducting GLP toxicology studies is essential, and you are familiar with outsourced development and regulatory requirements. Experience as a Sponsor Monitor or Study Director is highly valued.

You are an experienced scientific writer with solid knowledge of regulatory documentation. You are able to author the full range of non-clinical documentation, e.g non-clinical overviews and summaries for regulatory submissions, and the non-clinical parts of the Investigator’s Brochure (IB). Experience of regulatory submissions is an advantage.

As a person, you are collaborative, structured and proactive. You enjoy coordinating complex projects, building strong relationships and working in a cross-functional, international and deadline-driven environment. Fluency in spoken and written English is required.

Camurus offers

This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other.

You will have a broad area of responsibility and drive multiple non-clinical programs, working closely with leading international CROs and cross-functional development teams. With your toxicology background you will have a crucial role in R&D related activities.

Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment.

Information and application

For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/.

We are looking forward to seeing your application!

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn.

In this role, you will join the Non-Clinical Development team in Lund and contribute to the development of innovative medicines in a dynamic and collaborative environment. You will play a central role in the toxicological strategy for Camurus' products, working closely with colleagues across multiple disciplines as well as external partners.

We are looking for an experienced Senior Research Scientist, Toxicology to join our Non-Clinical Development team.

This is a strategic and cross-functional role where you will be responsible for developing non-clinical plans, designing toxicology programs and coordinating outsourced non-GLP and GLP toxicology studies performed by Contract Research Organizations (CROs). Acting as Sponsor Monitor, you will oversee study design, study conduct, data review and final reports, ensuring scientific quality, regulatory compliance and timely delivery. You will also contribute to regulatory submissions by preparing and reviewing non-clinical documentation and representing Non-Clinical Development in product development teams.

Main responsibility Among others, your responsibilities will include:

· Develop toxicology strategies and non-clinical development plans.

· Design and monitor outsourced GLP studies.

· Select, manage and collaborate with international CRO partners.

· Prepare and review toxicology reports and regulatory documentation.

· Represent Non-Clinical Development in cross-functional development teams.

· Ensure compliance with GLP and international regulatory requirements (ICH, FDA, EMA and OECD).

Candidate profile You hold a PhD or MSc in Toxicology, Pharmacology or another relevant Life Science discipline.

You have several years of experience from non-clinical drug development within the pharmaceutical, biotechnology or CRO industry. Experience of planning, monitoring or conducting GLP toxicology studies is essential, and you are familiar with outsourced development and regulatory requirements. Experience as a Sponsor Monitor or Study Director is highly valued.

You are an experienced scientific writer with solid knowledge of regulatory documentation. You are able to author the full range of non-clinical documentation, e.g non-clinical overviews and summaries for regulatory submissions, and the non-clinical parts of the Investigator’s Brochure (IB). Experience of regulatory submissions is an advantage.

As a person, you are collaborative, structured and proactive. You enjoy coordinating complex projects, building strong relationships and working in a cross-functional, international and deadline-driven environment. Fluency in spoken and written English is required.

Camurus offers

This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other.

You will have a broad area of responsibility and drive multiple non-clinical programs, working closely with leading international CROs and cross-functional development teams. With your toxicology background you will have a crucial role in R&D related activities.

Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment.

Information and application

For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/.

We are looking forward to seeing your application!

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.

Learn about the Danaher Business System which makes everything possible.

Background

At Cytiva R&D in Uppsala, we develop Biacore™ systems that enable scientists worldwide to generate world-class, label-free interaction analysis data. For more than 35 years, Biacore technology has been a leader in biomolecular interaction analysis, helping advance drug discovery and life science research. A key part of our mission is to push the boundaries of what is possible through the development of innovative applications, methodologies, and consumables that expand the capabilities and value of Biacore systems.

About the Role

We are looking for a passionate and experienced Senior Research Engineer to join our Biacore Applications & Consumables team. In this role, you will have the opportunity to shape the next generation of Biacore consumables, turning new ideas into products that enable scientific breakthroughs for researchers around the globe.

As part of a collaborative and highly skilled team, you will drive innovation from concept to product, combining hands-on laboratory work, scientific expertise, and creative problem-solving to develop solutions that make a real impact. You will also play an important role in supporting and continuously improving our existing consumables portfolio, ensuring that Biacore remains the trusted choice for interaction analysis.

What You'll Do

• Drive the development of innovative Biacore consumables products from idea to launch.
• Design, evaluate, and optimize new consumables concepts and technologies.
• Solve scientific and technical challenges through experimentation and innovation.
• Perform hands-on laboratory work to develop and validate new products and applications.
• Collaborate closely with cross-functional teams to deliver customer-focused solutions.
• Support product care activities and contribute to the continuous improvement of our consumables portfolio.

Who You Are

• MSc or similar in relevant life science discipline.
• Experience working with SPR technology and Biacore systems.
• Strong laboratory skills and a genuine passion for experimental science.
• Knowledge of statistics and data analysis, with an interest in applying them to product development.
• An innovative problem-solver who enjoys turning scientific challenges into practical solutions.
• Strong communication and presentation skills.
• Fluent in Swedish and English, both written and spoken.
• A collaborative team player who thrives in a multidisciplinary environment.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.

Learn about the Danaher Business System which makes everything possible.

Background

At Cytiva R&D in Uppsala, we develop Biacore™ systems that enable scientists worldwide to generate world-class, label-free interaction analysis data. For more than 35 years, Biacore technology has been a leader in biomolecular interaction analysis, helping advance drug discovery and life science research. A key part of our mission is to push the boundaries of what is possible through the development of innovative applications, methodologies, and consumables that expand the capabilities and value of Biacore systems.

About the Role

We are looking for a passionate and experienced Senior Research Engineer to join our Biacore Applications & Consumables team. In this role, you will have the opportunity to shape the next generation of Biacore consumables, turning new ideas into products that enable scientific breakthroughs for researchers around the globe.

As part of a collaborative and highly skilled team, you will drive innovation from concept to product, combining hands-on laboratory work, scientific expertise, and creative problem-solving to develop solutions that make a real impact. You will also play an important role in supporting and continuously improving our existing consumables portfolio, ensuring that Biacore remains the trusted choice for interaction analysis.

What You'll Do

• Drive the development of innovative Biacore consumables products from idea to launch.
• Design, evaluate, and optimize new consumables concepts and technologies.
• Solve scientific and technical challenges through experimentation and innovation.
• Perform hands-on laboratory work to develop and validate new products and applications.
• Collaborate closely with cross-functional teams to deliver customer-focused solutions.
• Support product care activities and contribute to the continuous improvement of our consumables portfolio.

Who You Are

• MSc or similar in relevant life science discipline.
• Experience working with SPR technology and Biacore systems.
• Strong laboratory skills and a genuine passion for experimental science.
• Knowledge of statistics and data analysis, with an interest in applying them to product development.
• An innovative problem-solver who enjoys turning scientific challenges into practical solutions.
• Strong communication and presentation skills.
• Fluent in Swedish and English, both written and spoken.
• A collaborative team player who thrives in a multidisciplinary environment.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.

Learn about the Danaher Business System which makes everything possible.

Background

At Cytiva R&D in Uppsala, we develop Biacore™ systems that enable scientists worldwide to generate world-class, label-free interaction analysis data. For more than 35 years, Biacore technology has been a leader in biomolecular interaction analysis, helping advance drug discovery and life science research. A key part of our mission is to push the boundaries of what is possible through the development of innovative applications, methodologies, and consumables that expand the capabilities and value of Biacore systems.

About the Role

We are looking for a passionate and experienced Senior Research Engineer to join our Biacore Applications & Consumables team. In this role, you will have the opportunity to shape the next generation of Biacore consumables, turning new ideas into products that enable scientific breakthroughs for researchers around the globe.

As part of a collaborative and highly skilled team, you will drive innovation from concept to product, combining hands-on laboratory work, scientific expertise, and creative problem-solving to develop solutions that make a real impact. You will also play an important role in supporting and continuously improving our existing consumables portfolio, ensuring that Biacore remains the trusted choice for interaction analysis.

What You'll Do

• Drive the development of innovative Biacore consumables products from idea to launch.
• Design, evaluate, and optimize new consumables concepts and technologies.
• Solve scientific and technical challenges through experimentation and innovation.
• Perform hands-on laboratory work to develop and validate new products and applications.
• Collaborate closely with cross-functional teams to deliver customer-focused solutions.
• Support product care activities and contribute to the continuous improvement of our consumables portfolio.

Who You Are

• MSc or similar in relevant life science discipline.
• Experience working with SPR technology and Biacore systems.
• Strong laboratory skills and a genuine passion for experimental science.
• Knowledge of statistics and data analysis, with an interest in applying them to product development.
• An innovative problem-solver who enjoys turning scientific challenges into practical solutions.
• Strong communication and presentation skills.
• Fluent in Swedish and English, both written and spoken.
• A collaborative team player who thrives in a multidisciplinary environment.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.

Learn about the Danaher Business System which makes everything possible.

Background

At Cytiva R&D in Uppsala, we develop Biacore™ systems that enable scientists worldwide to generate world-class, label-free interaction analysis data. For more than 35 years, Biacore technology has been a leader in biomolecular interaction analysis, helping advance drug discovery and life science research. A key part of our mission is to push the boundaries of what is possible through the development of innovative applications, methodologies, and consumables that expand the capabilities and value of Biacore systems.

About the Role

We are looking for a passionate and experienced Senior Research Engineer to join our Biacore Applications & Consumables team. In this role, you will have the opportunity to shape the next generation of Biacore consumables, turning new ideas into products that enable scientific breakthroughs for researchers around the globe.

As part of a collaborative and highly skilled team, you will drive innovation from concept to product, combining hands-on laboratory work, scientific expertise, and creative problem-solving to develop solutions that make a real impact. You will also play an important role in supporting and continuously improving our existing consumables portfolio, ensuring that Biacore remains the trusted choice for interaction analysis.

What You'll Do

• Drive the development of innovative Biacore consumables products from idea to launch.
• Design, evaluate, and optimize new consumables concepts and technologies.
• Solve scientific and technical challenges through experimentation and innovation.
• Perform hands-on laboratory work to develop and validate new products and applications.
• Collaborate closely with cross-functional teams to deliver customer-focused solutions.
• Support product care activities and contribute to the continuous improvement of our consumables portfolio.

Who You Are

• MSc or similar in relevant life science discipline.
• Experience working with SPR technology and Biacore systems.
• Strong laboratory skills and a genuine passion for experimental science.
• Knowledge of statistics and data analysis, with an interest in applying them to product development.
• An innovative problem-solver who enjoys turning scientific challenges into practical solutions.
• Strong communication and presentation skills.
• Fluent in Swedish and English, both written and spoken.
• A collaborative team player who thrives in a multidisciplinary environment.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.

Learn about the Danaher Business System which makes everything possible.

Background

At Cytiva R&D in Uppsala, we develop Biacore™ systems that enable scientists worldwide to generate world-class, label-free interaction analysis data. For more than 35 years, Biacore technology has been a leader in biomolecular interaction analysis, helping advance drug discovery and life science research. A key part of our mission is to push the boundaries of what is possible through the development of innovative applications, methodologies, and consumables that expand the capabilities and value of Biacore systems.

About the Role

We are looking for a passionate and experienced Senior Research Engineer to join our Biacore Applications & Consumables team. In this role, you will have the opportunity to shape the next generation of Biacore consumables, turning new ideas into products that enable scientific breakthroughs for researchers around the globe.

As part of a collaborative and highly skilled team, you will drive innovation from concept to product, combining hands-on laboratory work, scientific expertise, and creative problem-solving to develop solutions that make a real impact. You will also play an important role in supporting and continuously improving our existing consumables portfolio, ensuring that Biacore remains the trusted choice for interaction analysis.

What You'll Do

• Drive the development of innovative Biacore consumables products from idea to launch.
• Design, evaluate, and optimize new consumables concepts and technologies.
• Solve scientific and technical challenges through experimentation and innovation.
• Perform hands-on laboratory work to develop and validate new products and applications.
• Collaborate closely with cross-functional teams to deliver customer-focused solutions.
• Support product care activities and contribute to the continuous improvement of our consumables portfolio.

Who You Are

• MSc or similar in relevant life science discipline.
• Experience working with SPR technology and Biacore systems.
• Strong laboratory skills and a genuine passion for experimental science.
• Knowledge of statistics and data analysis, with an interest in applying them to product development.
• An innovative problem-solver who enjoys turning scientific challenges into practical solutions.
• Strong communication and presentation skills.
• Fluent in Swedish and English, both written and spoken.
• A collaborative team player who thrives in a multidisciplinary environment.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.