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0 lediga jobb som "Ingenjör" hos "QRIOS AB"

Quality Assurance (QA) Manager to Inossia AB
Arbetsgivare / Ort:QRIOS AB / Stockholm
Omfattning / Varaktighet:Vanlig anställning / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 30 december (5 månader och 18 dagar kvar)
Publicerad: 2026-07-03
Källa: Arbetsförmedlingen
Ansök här
Om jobbet
Inossia is now recruiting a Quality Assurance (QA) Manager to the company. The position is full-time and based in our headquartered office in Stockholm and we are looking for a new colleague to join the team at Inossia.
Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life. Inossia® provides vertebral augmentation solutions that have been adapted to the mechanical properties of bone that will give Better fracture treatment for Osteporotic Bone. The company is entering a pivotal phase of its growth, with the upcoming launch of its first product and the transition from development to commercial operations. While moving toward market introduction, the company remains committed to ongoing research and development to advance solutions in spine care
As a QA Manager, you will be responsible for managing our QMS and overseeing product releases. You will lead training on new SOPs and collaborate closely with our Production Manager to ensure accurate and compliant documentation. Additionally, your responsibilities will include preparing the organization for audits and conducting supplier audits.
At Inossia, you will get the unique opportunity to build, shape and optimize our processes from the inside out, make a positive impact and apply your experience and expertise within QA to ensure the highest quality standards. If this sounds interesting to you - Come join us and be part of our mission of improving fracture treatment for osteoporotic patients so that they can live an active life.
We will interview candidates continuously and welcome your application today!
Responsibilities
The QA Manager will have a central role in oversight and management of manufacturing and analytical activities from a quality perspective. You will report directly to the Director of QA/RA at Inossia.
Your main responsibilities will include:
Lead, maintain, and continuously improve the Quality Management System in accordance with ISO 13485 and applicable medical device regulations
Ensure compliance throughout the medical device product lifecycle, from development and design through manufacturing, release, and post-market activities
Oversee risk management activities, including risk files, benefit-risk analysis, and lifecycle updates
Plan, conduct, and support internal and external audits, including notified body, supplier, and regulatory audits
Act as a key point of contact for audit readiness, responses, and corrective actions
Manage CAPA, non-conformances, deviations, and change control processes
Collaborate cross-functionally to ensure quality is embedded across the organisation
Support supplier quality management, qualification, and ongoing performance monitoring
Ensure robust documentation control, version management, and data integrity
Contribute to key strategic developments within the QA department.
Your Profile
Key Qualifications for the position include:
Multiple years of QA experience within the medical device industry, preferably in a smaller-sized company
Strong hands-on knowledge of ISO 13485 and ISO 14971
Proven experience leading and supporting audits and inspections
Solid understanding of medical device quality systems, risk management, and product development processes
Experience working in cross-functional, international environments
Fluency in English, both in speaking and in writing
We are looking for someone with a can-do attitude, strong organizational skills and a quality-driven mindset. You enjoy taking ownership and accountability to drive continuous improvement of the quality system and work well both independently and in team settings. You can handle multiple tasks and manage priorities in a timely manner and have excellent collaboration and communication skills. You are analytical, detail- and result-oriented and can effectively combine flexibility with a strong decision-making ability. Importantly, you enjoy a dynamic place of work where people matter, and your contributions will make a positive impact.
If you are passionate about making a difference in the lives of patients and have the skills and experience to excel in this role, we invite you to apply today!
About Inossia AB
Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life.
Inossia is entering a pivotal phase of its growth, with the upcoming launch of its first product and the transition from development to commercial operations. While moving toward market introduction, the company remains committed to ongoing research and development to advance solutions in spine care
Inossia has completed a clinical study of 196 patients in 4 countries and 9 clinics
Inossia received the Breakthrough Device Designation for Inossia Cement Softener in June 2025
To learn more, please visit www.Inossia.com
For more information about the position, please contact:
Krishan Johansson Haque, PhD
Sr Recruitment Consultant, QRIOS Life Science & Engineering
T: +46 (0)72-070 16 53
E: krishan.johansson-haque@qrios.se
Arbetsgivare
QRIOS AB
Vasagatan 7
11120 Stockholm
Webbplats: https://karriar.qrios.se
Ansökan
Ansök senast 30 december (5 månader och 18 dagar kvar)
Ansök här
Quality Assurance (QA) Manager to Inossia AB
Arbetsgivare / Ort:QRIOS AB / Stockholm
Omfattning / Varaktighet:Vanlig anställning / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 30 december (5 månader och 18 dagar kvar)
Publicerad: 2026-07-03
Källa: Arbetsförmedlingen
Ansök här
Om jobbet
Inossia is now recruiting a Quality Assurance (QA) Manager to the company. The position is full-time and based in our headquartered office in Stockholm and we are looking for a new colleague to join the team at Inossia.
Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life. Inossia® provides vertebral augmentation solutions that have been adapted to the mechanical properties of bone that will give Better fracture treatment for Osteporotic Bone. The company is entering a pivotal phase of its growth, with the upcoming launch of its first product and the transition from development to commercial operations. While moving toward market introduction, the company remains committed to ongoing research and development to advance solutions in spine care
As a QA Manager, you will be responsible for managing our QMS and overseeing product releases. You will lead training on new SOPs and collaborate closely with our Production Manager to ensure accurate and compliant documentation. Additionally, your responsibilities will include preparing the organization for audits and conducting supplier audits.
At Inossia, you will get the unique opportunity to build, shape and optimize our processes from the inside out, make a positive impact and apply your experience and expertise within QA to ensure the highest quality standards. If this sounds interesting to you - Come join us and be part of our mission of improving fracture treatment for osteoporotic patients so that they can live an active life.
We will interview candidates continuously and welcome your application today!
Responsibilities
The QA Manager will have a central role in oversight and management of manufacturing and analytical activities from a quality perspective. You will report directly to the Director of QA/RA at Inossia.
Your main responsibilities will include:
Lead, maintain, and continuously improve the Quality Management System in accordance with ISO 13485 and applicable medical device regulations
Ensure compliance throughout the medical device product lifecycle, from development and design through manufacturing, release, and post-market activities
Oversee risk management activities, including risk files, benefit-risk analysis, and lifecycle updates
Plan, conduct, and support internal and external audits, including notified body, supplier, and regulatory audits
Act as a key point of contact for audit readiness, responses, and corrective actions
Manage CAPA, non-conformances, deviations, and change control processes
Collaborate cross-functionally to ensure quality is embedded across the organisation
Support supplier quality management, qualification, and ongoing performance monitoring
Ensure robust documentation control, version management, and data integrity
Contribute to key strategic developments within the QA department.
Your Profile
Key Qualifications for the position include:
Multiple years of QA experience within the medical device industry, preferably in a smaller-sized company
Strong hands-on knowledge of ISO 13485 and ISO 14971
Proven experience leading and supporting audits and inspections
Solid understanding of medical device quality systems, risk management, and product development processes
Experience working in cross-functional, international environments
Fluency in English, both in speaking and in writing
We are looking for someone with a can-do attitude, strong organizational skills and a quality-driven mindset. You enjoy taking ownership and accountability to drive continuous improvement of the quality system and work well both independently and in team settings. You can handle multiple tasks and manage priorities in a timely manner and have excellent collaboration and communication skills. You are analytical, detail- and result-oriented and can effectively combine flexibility with a strong decision-making ability. Importantly, you enjoy a dynamic place of work where people matter, and your contributions will make a positive impact.
If you are passionate about making a difference in the lives of patients and have the skills and experience to excel in this role, we invite you to apply today!
About Inossia AB
Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life.
Inossia is entering a pivotal phase of its growth, with the upcoming launch of its first product and the transition from development to commercial operations. While moving toward market introduction, the company remains committed to ongoing research and development to advance solutions in spine care
Inossia has completed a clinical study of 196 patients in 4 countries and 9 clinics
Inossia received the Breakthrough Device Designation for Inossia Cement Softener in June 2025
To learn more, please visit www.Inossia.com
For more information about the position, please contact:
Krishan Johansson Haque, PhD
Sr Recruitment Consultant, QRIOS Life Science & Engineering
T: +46 (0)72-070 16 53
E: krishan.johansson-haque@qrios.se
Arbetsgivare
QRIOS AB
Vasagatan 7
11120 Stockholm
Webbplats: https://karriar.qrios.se
Ansökan
Ansök senast 30 december (5 månader och 18 dagar kvar)
Ansök här
CMC - Lead to Intervacc
Arbetsgivare / Ort:QRIOS AB / Stockholm
Omfattning / Varaktighet:Vanlig anställning / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 31 augusti (1 månad och 19 dagar kvar)
Publicerad: 2026-07-03
Källa: Arbetsförmedlingen
Ansök här
Om jobbet
At Intervacc, we are pioneering the next generation of veterinary vaccines through our proprietary technology platform. Rooted in research from the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), our mission is to reduce the impact of bacterial infections in animals through innovative, effective, and safe vaccines.
Our first proprietary product — a vaccine against strangles, a serious streptococcal infection in horses— is now available in several European markets. This is just the beginning. We are expanding our reach into new territories and broadening our product portfolio.
We have an exciting new opportunity for an experienced CMC Lead who will be responsible for the manufacturing and testing for the company’s marketed products, as well as the CMC-strategy for development of new vaccine products. The CMC Lead will have a central role in providing scientific guidance, support, and expertise for all CMC activities including commercial products and product under development. You will work with products in different markets to fulfill a key role within our dedicated, friendly and experienced team. If this sounds interesting to you – come join us!
Intervacc AB is headquartered in Stockholm Sweden and is listed on the Swedish Nasdaq First North Growth Market. The position is full-time, and we welcome your application today!
Key responsibilities
As a CMC Lead, you will provide CMC strategy and expertise for our development and marketed products to ensure the company’s products are developed, manufactured, tested and maintained in compliance with global regulatory expectations, requirements and guidance.
Duties and responsibilities include:
Responsibility of delivering CMC-parts of development projects, launch projects as well as projects/products in commercial phase
Developing CMC-strategies and ensuring oversight and planning of work performed at CROs/CMOs related to development, analytical testing and manufacturing of products
Monitor KPIs and ensure timely delivery of data to support development, manufacturing and release
Being responsible and promote using modern processing analytical principles such as Quality by Design, risk-based method development and data-driven decision making.
Working with other internal functions as well as external suppliers and partners to ensure CMC-deliverables and resolve arising issues
Participating in budget planning and monitoring
Ensure compliance with global regulatory requirements and support regulatory inspections and audits
Skills and Competencies
The suitable candidate has the following qualifications:
Formal academic degree level (MSc., Ph.D) in a science-related subject e.g. pharmacy, biology or chemistry
Significant experience (more than 7-10 years) in development, manufacturing and analytical testing of biologics or biotechnology-derived products e.g. vaccines from the pharmaceutical industry
Significant knowledge of the drug development and manufacturing process for biologics (including upstream and downstream processes and analytical methods)
Expert knowledge in analytical and/or process development for biologics
Understanding of supply planning and supplier management
Knowledge of current regulatory CMC requirements, and solid knowledge in understanding of regulations and guidance for the manufacturing of biotechnology products
Excellent communication and documentation skills in English are required
The successful candidate for this position will be someone who:
Has a solid scientific background with significant experience in processing and analytical testing of biotechnology products in combination with project management skills
Is analytical, solution-oriented with a strong personal drive
Is structured and organized
Has a good eye for detail and a thorough approach to work
Is a proactive, flexible, motivated and ambitious team player with ability to drive change
If you are ready to bring your expertise within the CMC area for biologics, we are ready to offer you an excellent career opportunity at an innovative company with an exciting journey ahead!
About Intervacc:
Intervacc is an innovative Swedish biotechnology company that develops and markets modern, effective, and safe vaccines against bacterial infections affecting animals. Over the past decade, advances in molecular biology techniques have significantly enhanced our ability to investigate the genomes of pathogenic bacteria. Building on our research foundations at the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), we have developed a technology platform for a new generation of vaccines. Our first proprietary vaccine, a vaccine against the streptococcal infection strangles, which affects horses—is now available in several European markets. The Intervacc share (STO: IVACC) is listed on the NASDAQ First North Growth Market and our headquarter is in Stockholm, Sweden. You can find more information about Intervacc at www.intervacc.se
For more information about this position, please contact:
Krishan Johansson Haque, PhD
Sr Recruitment Consultant, QRIOS Life Science & Engineering
T: +46 (0)72-070 16 53
E: krishan.johansson-haque@qrios.se
Arbetsgivare
QRIOS AB
Vasagatan 7
11120 Stockholm
Webbplats: https://karriar.qrios.se
Ansökan
Ansök senast 31 augusti (1 månad och 19 dagar kvar)
Ansök här
CMC - Lead to Intervacc
Arbetsgivare / Ort:QRIOS AB / Stockholm
Omfattning / Varaktighet:Vanlig anställning / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 31 augusti (1 månad och 19 dagar kvar)
Publicerad: 2026-07-03
Källa: Arbetsförmedlingen
Ansök här
Om jobbet
At Intervacc, we are pioneering the next generation of veterinary vaccines through our proprietary technology platform. Rooted in research from the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), our mission is to reduce the impact of bacterial infections in animals through innovative, effective, and safe vaccines.
Our first proprietary product — a vaccine against strangles, a serious streptococcal infection in horses— is now available in several European markets. This is just the beginning. We are expanding our reach into new territories and broadening our product portfolio.
We have an exciting new opportunity for an experienced CMC Lead who will be responsible for the manufacturing and testing for the company’s marketed products, as well as the CMC-strategy for development of new vaccine products. The CMC Lead will have a central role in providing scientific guidance, support, and expertise for all CMC activities including commercial products and product under development. You will work with products in different markets to fulfill a key role within our dedicated, friendly and experienced team. If this sounds interesting to you – come join us!
Intervacc AB is headquartered in Stockholm Sweden and is listed on the Swedish Nasdaq First North Growth Market. The position is full-time, and we welcome your application today!
Key responsibilities
As a CMC Lead, you will provide CMC strategy and expertise for our development and marketed products to ensure the company’s products are developed, manufactured, tested and maintained in compliance with global regulatory expectations, requirements and guidance.
Duties and responsibilities include:
Responsibility of delivering CMC-parts of development projects, launch projects as well as projects/products in commercial phase
Developing CMC-strategies and ensuring oversight and planning of work performed at CROs/CMOs related to development, analytical testing and manufacturing of products
Monitor KPIs and ensure timely delivery of data to support development, manufacturing and release
Being responsible and promote using modern processing analytical principles such as Quality by Design, risk-based method development and data-driven decision making.
Working with other internal functions as well as external suppliers and partners to ensure CMC-deliverables and resolve arising issues
Participating in budget planning and monitoring
Ensure compliance with global regulatory requirements and support regulatory inspections and audits
Skills and Competencies
The suitable candidate has the following qualifications:
Formal academic degree level (MSc., Ph.D) in a science-related subject e.g. pharmacy, biology or chemistry
Significant experience (more than 7-10 years) in development, manufacturing and analytical testing of biologics or biotechnology-derived products e.g. vaccines from the pharmaceutical industry
Significant knowledge of the drug development and manufacturing process for biologics (including upstream and downstream processes and analytical methods)
Expert knowledge in analytical and/or process development for biologics
Understanding of supply planning and supplier management
Knowledge of current regulatory CMC requirements, and solid knowledge in understanding of regulations and guidance for the manufacturing of biotechnology products
Excellent communication and documentation skills in English are required
The successful candidate for this position will be someone who:
Has a solid scientific background with significant experience in processing and analytical testing of biotechnology products in combination with project management skills
Is analytical, solution-oriented with a strong personal drive
Is structured and organized
Has a good eye for detail and a thorough approach to work
Is a proactive, flexible, motivated and ambitious team player with ability to drive change
If you are ready to bring your expertise within the CMC area for biologics, we are ready to offer you an excellent career opportunity at an innovative company with an exciting journey ahead!
About Intervacc:
Intervacc is an innovative Swedish biotechnology company that develops and markets modern, effective, and safe vaccines against bacterial infections affecting animals. Over the past decade, advances in molecular biology techniques have significantly enhanced our ability to investigate the genomes of pathogenic bacteria. Building on our research foundations at the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), we have developed a technology platform for a new generation of vaccines. Our first proprietary vaccine, a vaccine against the streptococcal infection strangles, which affects horses—is now available in several European markets. The Intervacc share (STO: IVACC) is listed on the NASDAQ First North Growth Market and our headquarter is in Stockholm, Sweden. You can find more information about Intervacc at www.intervacc.se
For more information about this position, please contact:
Krishan Johansson Haque, PhD
Sr Recruitment Consultant, QRIOS Life Science & Engineering
T: +46 (0)72-070 16 53
E: krishan.johansson-haque@qrios.se
Arbetsgivare
QRIOS AB
Vasagatan 7
11120 Stockholm
Webbplats: https://karriar.qrios.se
Ansökan
Ansök senast 31 augusti (1 månad och 19 dagar kvar)
Ansök här
Quality Assurance (QA) Manager to Inossia AB
Arbetsgivare / Ort:QRIOS AB / Stockholm
Omfattning / Varaktighet:Vanlig anställning / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 30 december (5 månader och 18 dagar kvar)
Publicerad: 2026-07-03
Källa: Arbetsförmedlingen
Ansök här
Om jobbet
Inossia is now recruiting a Quality Assurance (QA) Manager to the company. The position is full-time and based in our headquartered office in Stockholm and we are looking for a new colleague to join the team at Inossia.
Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life. Inossia® provides vertebral augmentation solutions that have been adapted to the mechanical properties of bone that will give Better fracture treatment for Osteporotic Bone. The company is entering a pivotal phase of its growth, with the upcoming launch of its first product and the transition from development to commercial operations. While moving toward market introduction, the company remains committed to ongoing research and development to advance solutions in spine care
As a QA Manager, you will be responsible for managing our QMS and overseeing product releases. You will lead training on new SOPs and collaborate closely with our Production Manager to ensure accurate and compliant documentation. Additionally, your responsibilities will include preparing the organization for audits and conducting supplier audits.
At Inossia, you will get the unique opportunity to build, shape and optimize our processes from the inside out, make a positive impact and apply your experience and expertise within QA to ensure the highest quality standards. If this sounds interesting to you - Come join us and be part of our mission of improving fracture treatment for osteoporotic patients so that they can live an active life.
We will interview candidates continuously and welcome your application today!
Responsibilities
The QA Manager will have a central role in oversight and management of manufacturing and analytical activities from a quality perspective. You will report directly to the Director of QA/RA at Inossia.
Your main responsibilities will include:
Lead, maintain, and continuously improve the Quality Management System in accordance with ISO 13485 and applicable medical device regulations
Ensure compliance throughout the medical device product lifecycle, from development and design through manufacturing, release, and post-market activities
Oversee risk management activities, including risk files, benefit-risk analysis, and lifecycle updates
Plan, conduct, and support internal and external audits, including notified body, supplier, and regulatory audits
Act as a key point of contact for audit readiness, responses, and corrective actions
Manage CAPA, non-conformances, deviations, and change control processes
Collaborate cross-functionally to ensure quality is embedded across the organisation
Support supplier quality management, qualification, and ongoing performance monitoring
Ensure robust documentation control, version management, and data integrity
Contribute to key strategic developments within the QA department.
Your Profile
Key Qualifications for the position include:
Multiple years of QA experience within the medical device industry, preferably in a smaller-sized company
Strong hands-on knowledge of ISO 13485 and ISO 14971
Proven experience leading and supporting audits and inspections
Solid understanding of medical device quality systems, risk management, and product development processes
Experience working in cross-functional, international environments
Fluency in English, both in speaking and in writing
We are looking for someone with a can-do attitude, strong organizational skills and a quality-driven mindset. You enjoy taking ownership and accountability to drive continuous improvement of the quality system and work well both independently and in team settings. You can handle multiple tasks and manage priorities in a timely manner and have excellent collaboration and communication skills. You are analytical, detail- and result-oriented and can effectively combine flexibility with a strong decision-making ability. Importantly, you enjoy a dynamic place of work where people matter, and your contributions will make a positive impact.
If you are passionate about making a difference in the lives of patients and have the skills and experience to excel in this role, we invite you to apply today!
About Inossia AB
Inossia aims at improving fracture treatment for osteoporotic patients so that they can live an active life.
Inossia is entering a pivotal phase of its growth, with the upcoming launch of its first product and the transition from development to commercial operations. While moving toward market introduction, the company remains committed to ongoing research and development to advance solutions in spine care
Inossia has completed a clinical study of 196 patients in 4 countries and 9 clinics
Inossia received the Breakthrough Device Designation for Inossia Cement Softener in June 2025
To learn more, please visit www.Inossia.com
For more information about the position, please contact:
Krishan Johansson Haque, PhD
Sr Recruitment Consultant, QRIOS Life Science & Engineering
T: +46 (0)72-070 16 53
E: krishan.johansson-haque@qrios.se
Arbetsgivare
QRIOS AB
Vasagatan 7
11120 Stockholm
Webbplats: https://karriar.qrios.se
Ansökan
Ansök senast 30 december (5 månader och 18 dagar kvar)
Ansök här
CMC - Lead to Intervacc
Arbetsgivare / Ort:QRIOS AB / Stockholm
Omfattning / Varaktighet:Vanlig anställning / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 31 augusti (1 månad och 19 dagar kvar)
Publicerad: 2026-07-03
Källa: Arbetsförmedlingen
Ansök här
Om jobbet
At Intervacc, we are pioneering the next generation of veterinary vaccines through our proprietary technology platform. Rooted in research from the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), our mission is to reduce the impact of bacterial infections in animals through innovative, effective, and safe vaccines.
Our first proprietary product — a vaccine against strangles, a serious streptococcal infection in horses— is now available in several European markets. This is just the beginning. We are expanding our reach into new territories and broadening our product portfolio.
We have an exciting new opportunity for an experienced CMC Lead who will be responsible for the manufacturing and testing for the company’s marketed products, as well as the CMC-strategy for development of new vaccine products. The CMC Lead will have a central role in providing scientific guidance, support, and expertise for all CMC activities including commercial products and product under development. You will work with products in different markets to fulfill a key role within our dedicated, friendly and experienced team. If this sounds interesting to you – come join us!
Intervacc AB is headquartered in Stockholm Sweden and is listed on the Swedish Nasdaq First North Growth Market. The position is full-time, and we welcome your application today!
Key responsibilities
As a CMC Lead, you will provide CMC strategy and expertise for our development and marketed products to ensure the company’s products are developed, manufactured, tested and maintained in compliance with global regulatory expectations, requirements and guidance.
Duties and responsibilities include:
Responsibility of delivering CMC-parts of development projects, launch projects as well as projects/products in commercial phase
Developing CMC-strategies and ensuring oversight and planning of work performed at CROs/CMOs related to development, analytical testing and manufacturing of products
Monitor KPIs and ensure timely delivery of data to support development, manufacturing and release
Being responsible and promote using modern processing analytical principles such as Quality by Design, risk-based method development and data-driven decision making.
Working with other internal functions as well as external suppliers and partners to ensure CMC-deliverables and resolve arising issues
Participating in budget planning and monitoring
Ensure compliance with global regulatory requirements and support regulatory inspections and audits
Skills and Competencies
The suitable candidate has the following qualifications:
Formal academic degree level (MSc., Ph.D) in a science-related subject e.g. pharmacy, biology or chemistry
Significant experience (more than 7-10 years) in development, manufacturing and analytical testing of biologics or biotechnology-derived products e.g. vaccines from the pharmaceutical industry
Significant knowledge of the drug development and manufacturing process for biologics (including upstream and downstream processes and analytical methods)
Expert knowledge in analytical and/or process development for biologics
Understanding of supply planning and supplier management
Knowledge of current regulatory CMC requirements, and solid knowledge in understanding of regulations and guidance for the manufacturing of biotechnology products
Excellent communication and documentation skills in English are required
The successful candidate for this position will be someone who:
Has a solid scientific background with significant experience in processing and analytical testing of biotechnology products in combination with project management skills
Is analytical, solution-oriented with a strong personal drive
Is structured and organized
Has a good eye for detail and a thorough approach to work
Is a proactive, flexible, motivated and ambitious team player with ability to drive change
If you are ready to bring your expertise within the CMC area for biologics, we are ready to offer you an excellent career opportunity at an innovative company with an exciting journey ahead!
About Intervacc:
Intervacc is an innovative Swedish biotechnology company that develops and markets modern, effective, and safe vaccines against bacterial infections affecting animals. Over the past decade, advances in molecular biology techniques have significantly enhanced our ability to investigate the genomes of pathogenic bacteria. Building on our research foundations at the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), we have developed a technology platform for a new generation of vaccines. Our first proprietary vaccine, a vaccine against the streptococcal infection strangles, which affects horses—is now available in several European markets. The Intervacc share (STO: IVACC) is listed on the NASDAQ First North Growth Market and our headquarter is in Stockholm, Sweden. You can find more information about Intervacc at www.intervacc.se
For more information about this position, please contact:
Krishan Johansson Haque, PhD
Sr Recruitment Consultant, QRIOS Life Science & Engineering
T: +46 (0)72-070 16 53
E: krishan.johansson-haque@qrios.se
Arbetsgivare
QRIOS AB
Vasagatan 7
11120 Stockholm
Webbplats: https://karriar.qrios.se
Ansökan
Ansök senast 31 augusti (1 månad och 19 dagar kvar)
Ansök här
CAD Development Engineer to Ascilion AB
Arbetsgivare / Ort:QRIOS AB / Stockholm
Omfattning / Varaktighet:Vanlig anställning / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 3 januari (5 månader och 22 dagar kvar)
Publicerad: 2026-07-07
Källa: Arbetsförmedlingen
Ansök här
Om jobbet
Are you a highly driven development engineer looking to join a core product development team working on new technology and product platforms?
Ascilion is now recruiting a CAD Development Engineer to the company. The position is full-time and based in our headquartered office in Kista and we are looking for a new colleague to join the Engineering group at Ascilion.
At Ascilion we are singularly focused on solving one of medicine’s big challenges: providing real-time access to molecular biomarkers. Ascilion’s proprietary and industry leading microneedle technology enables quick, reliable, and painless access to molecular biomarkers. Our dermal interstitial fluid (dISF) sampling platform can be tailored towards virtually any analytical or sensor technology used within products intended for spot measurement or wearables.
In this role, you will be deeply involved from concept to tested product, with responsibility for CAD design, prototyping, and hands-on verification in the lab. You will work closely with members within team but also cross-functionally with dedicated and highly skilled colleagues across multiple disciplines.
This is an excellent opportunity for you to join a competent and friendly development team and a growing company with an exciting journey ahead. If this sounds interesting to you, please contact us using the details below!
We will interview candidates continuously for the position and welcome your application today.
Responsibilities
The CAD Development Engineer will be a core member of the new product development team at Ascilion. You will report directly to the CTO of the company.
Your main responsibilities will include:
Responsibility for CAD design of mechanical and integrated product systems
Driving design from concept through prototyping and manufacturing
Participating actively in testing, evaluation, and iterative product development
Working closely with experts across multiple disciplines including mechanics, electrochemistry, electronics, MEMS, regulatory & quality, manufacturing, and system development
Your Profile
Key qualifications for the position include:
MSc in Mechanical Engineering or similar
Expert-level SolidWorks capability, should effectively be able to teach it
Strong experience designing for manufacturing, especially injection molded parts
Strong understanding of tolerances, manufacturability, and rapid iteration
Experience with semiconductor manufacturing and MEMS structures is a strong plus
Experience with analog electronics design is a strong plus
PCB layout experience is a strong plus
We are looking for creative and analytical and structured CAD-professional who enjoys working in a highly dynamic and development environment. As a person, you are curious, problem-solving and solution-oriented, with a strong sense of ownership and accountability. You have strong execution focus as well as strong communication and collaboration skills. You enjoy testing what has been designed and believe that great products are created when top experts from different disciplines work closely together.
At Ascilion, you will have the opportunity to make an impact not only in your own area of responsibility, but also on the development of the company as a whole.
About Ascilion
Ascilion was founded in 2012 with a mission to solve the problem of sampling dermal interstitial fluid in an efficient and pain-free way. A team of engineers with deep experience in MEMS technology and microfluidics took on the challenge of solving what turned out to be a very complex problem.
We exist to bridge the worlds of precision engineering and biomarker science, creating innovative microneedle technologies that make dISF accessible, reliable, and painless; empowering researchers, clinicians, and companies to unlock the full potential of health monitoring and diagnostics.
We are currently in a very exciting expansion phase where we grow all aspects of the organization from R&D to sales. Our customer base is increasing with numerous close collaborations in Europe, the US and Asia. Come, join our journey!
To learn more about us please visit, www.ascilion.com
For more information about this position, please contact:
Krishan Johansson Haque, PhD
Sr Recruitment Consultant, QRIOS Life Science & Engineering
T: 0720701653
E: krishan.johansson-haque@qrios.se
Arbetsgivare
QRIOS AB
Vasagatan 7
11120 Stockholm
Webbplats: https://karriar.qrios.se
Ansökan
Ansök senast 3 januari (5 månader och 22 dagar kvar)
Ansök här
CAD Development Engineer to Ascilion AB
Arbetsgivare / Ort:QRIOS AB / Stockholm
Omfattning / Varaktighet:Vanlig anställning / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 3 januari (5 månader och 22 dagar kvar)
Publicerad: 2026-07-07
Källa: Arbetsförmedlingen
Ansök här
Om jobbet
Are you a highly driven development engineer looking to join a core product development team working on new technology and product platforms?
Ascilion is now recruiting a CAD Development Engineer to the company. The position is full-time and based in our headquartered office in Kista and we are looking for a new colleague to join the Engineering group at Ascilion.
At Ascilion we are singularly focused on solving one of medicine’s big challenges: providing real-time access to molecular biomarkers. Ascilion’s proprietary and industry leading microneedle technology enables quick, reliable, and painless access to molecular biomarkers. Our dermal interstitial fluid (dISF) sampling platform can be tailored towards virtually any analytical or sensor technology used within products intended for spot measurement or wearables.
In this role, you will be deeply involved from concept to tested product, with responsibility for CAD design, prototyping, and hands-on verification in the lab. You will work closely with members within team but also cross-functionally with dedicated and highly skilled colleagues across multiple disciplines.
This is an excellent opportunity for you to join a competent and friendly development team and a growing company with an exciting journey ahead. If this sounds interesting to you, please contact us using the details below!
We will interview candidates continuously for the position and welcome your application today.
Responsibilities
The CAD Development Engineer will be a core member of the new product development team at Ascilion. You will report directly to the CTO of the company.
Your main responsibilities will include:
Responsibility for CAD design of mechanical and integrated product systems
Driving design from concept through prototyping and manufacturing
Participating actively in testing, evaluation, and iterative product development
Working closely with experts across multiple disciplines including mechanics, electrochemistry, electronics, MEMS, regulatory & quality, manufacturing, and system development
Your Profile
Key qualifications for the position include:
MSc in Mechanical Engineering or similar
Expert-level SolidWorks capability, should effectively be able to teach it
Strong experience designing for manufacturing, especially injection molded parts
Strong understanding of tolerances, manufacturability, and rapid iteration
Experience with semiconductor manufacturing and MEMS structures is a strong plus
Experience with analog electronics design is a strong plus
PCB layout experience is a strong plus
We are looking for creative and analytical and structured CAD-professional who enjoys working in a highly dynamic and development environment. As a person, you are curious, problem-solving and solution-oriented, with a strong sense of ownership and accountability. You have strong execution focus as well as strong communication and collaboration skills. You enjoy testing what has been designed and believe that great products are created when top experts from different disciplines work closely together.
At Ascilion, you will have the opportunity to make an impact not only in your own area of responsibility, but also on the development of the company as a whole.
About Ascilion
Ascilion was founded in 2012 with a mission to solve the problem of sampling dermal interstitial fluid in an efficient and pain-free way. A team of engineers with deep experience in MEMS technology and microfluidics took on the challenge of solving what turned out to be a very complex problem.
We exist to bridge the worlds of precision engineering and biomarker science, creating innovative microneedle technologies that make dISF accessible, reliable, and painless; empowering researchers, clinicians, and companies to unlock the full potential of health monitoring and diagnostics.
We are currently in a very exciting expansion phase where we grow all aspects of the organization from R&D to sales. Our customer base is increasing with numerous close collaborations in Europe, the US and Asia. Come, join our journey!
To learn more about us please visit, www.ascilion.com
For more information about this position, please contact:
Krishan Johansson Haque, PhD
Sr Recruitment Consultant, QRIOS Life Science & Engineering
T: 0720701653
E: krishan.johansson-haque@qrios.se
Arbetsgivare
QRIOS AB
Vasagatan 7
11120 Stockholm
Webbplats: https://karriar.qrios.se
Ansökan
Ansök senast 3 januari (5 månader och 22 dagar kvar)
Ansök här
CAD Development Engineer to Ascilion AB
Arbetsgivare / Ort:QRIOS AB / Stockholm
Omfattning / Varaktighet:Vanlig anställning / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 3 januari (5 månader och 22 dagar kvar)
Publicerad: 2026-07-07
Källa: Arbetsförmedlingen
Ansök här
Om jobbet
Are you a highly driven development engineer looking to join a core product development team working on new technology and product platforms?
Ascilion is now recruiting a CAD Development Engineer to the company. The position is full-time and based in our headquartered office in Kista and we are looking for a new colleague to join the Engineering group at Ascilion.
At Ascilion we are singularly focused on solving one of medicine’s big challenges: providing real-time access to molecular biomarkers. Ascilion’s proprietary and industry leading microneedle technology enables quick, reliable, and painless access to molecular biomarkers. Our dermal interstitial fluid (dISF) sampling platform can be tailored towards virtually any analytical or sensor technology used within products intended for spot measurement or wearables.
In this role, you will be deeply involved from concept to tested product, with responsibility for CAD design, prototyping, and hands-on verification in the lab. You will work closely with members within team but also cross-functionally with dedicated and highly skilled colleagues across multiple disciplines.
This is an excellent opportunity for you to join a competent and friendly development team and a growing company with an exciting journey ahead. If this sounds interesting to you, please contact us using the details below!
We will interview candidates continuously for the position and welcome your application today.
Responsibilities
The CAD Development Engineer will be a core member of the new product development team at Ascilion. You will report directly to the CTO of the company.
Your main responsibilities will include:
Responsibility for CAD design of mechanical and integrated product systems
Driving design from concept through prototyping and manufacturing
Participating actively in testing, evaluation, and iterative product development
Working closely with experts across multiple disciplines including mechanics, electrochemistry, electronics, MEMS, regulatory & quality, manufacturing, and system development
Your Profile
Key qualifications for the position include:
MSc in Mechanical Engineering or similar
Expert-level SolidWorks capability, should effectively be able to teach it
Strong experience designing for manufacturing, especially injection molded parts
Strong understanding of tolerances, manufacturability, and rapid iteration
Experience with semiconductor manufacturing and MEMS structures is a strong plus
Experience with analog electronics design is a strong plus
PCB layout experience is a strong plus
We are looking for creative and analytical and structured CAD-professional who enjoys working in a highly dynamic and development environment. As a person, you are curious, problem-solving and solution-oriented, with a strong sense of ownership and accountability. You have strong execution focus as well as strong communication and collaboration skills. You enjoy testing what has been designed and believe that great products are created when top experts from different disciplines work closely together.
At Ascilion, you will have the opportunity to make an impact not only in your own area of responsibility, but also on the development of the company as a whole.
About Ascilion
Ascilion was founded in 2012 with a mission to solve the problem of sampling dermal interstitial fluid in an efficient and pain-free way. A team of engineers with deep experience in MEMS technology and microfluidics took on the challenge of solving what turned out to be a very complex problem.
We exist to bridge the worlds of precision engineering and biomarker science, creating innovative microneedle technologies that make dISF accessible, reliable, and painless; empowering researchers, clinicians, and companies to unlock the full potential of health monitoring and diagnostics.
We are currently in a very exciting expansion phase where we grow all aspects of the organization from R&D to sales. Our customer base is increasing with numerous close collaborations in Europe, the US and Asia. Come, join our journey!
To learn more about us please visit, www.ascilion.com
For more information about this position, please contact:
Krishan Johansson Haque, PhD
Sr Recruitment Consultant, QRIOS Life Science & Engineering
T: 0720701653
E: krishan.johansson-haque@qrios.se
Arbetsgivare
QRIOS AB
Vasagatan 7
11120 Stockholm
Webbplats: https://karriar.qrios.se
Ansökan
Ansök senast 3 januari (5 månader och 22 dagar kvar)
Ansök här
CAD Development Engineer to Ascilion AB
Arbetsgivare / Ort:QRIOS AB / Stockholm
Omfattning / Varaktighet:Vanlig anställning / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 3 januari (5 månader och 22 dagar kvar)
Publicerad: 2026-07-07
Källa: Arbetsförmedlingen
Ansök här
Om jobbet
Are you a highly driven development engineer looking to join a core product development team working on new technology and product platforms?
Ascilion is now recruiting a CAD Development Engineer to the company. The position is full-time and based in our headquartered office in Kista and we are looking for a new colleague to join the Engineering group at Ascilion.
At Ascilion we are singularly focused on solving one of medicine’s big challenges: providing real-time access to molecular biomarkers. Ascilion’s proprietary and industry leading microneedle technology enables quick, reliable, and painless access to molecular biomarkers. Our dermal interstitial fluid (dISF) sampling platform can be tailored towards virtually any analytical or sensor technology used within products intended for spot measurement or wearables.
In this role, you will be deeply involved from concept to tested product, with responsibility for CAD design, prototyping, and hands-on verification in the lab. You will work closely with members within team but also cross-functionally with dedicated and highly skilled colleagues across multiple disciplines.
This is an excellent opportunity for you to join a competent and friendly development team and a growing company with an exciting journey ahead. If this sounds interesting to you, please contact us using the details below!
We will interview candidates continuously for the position and welcome your application today.
Responsibilities
The CAD Development Engineer will be a core member of the new product development team at Ascilion. You will report directly to the CTO of the company.
Your main responsibilities will include:
Responsibility for CAD design of mechanical and integrated product systems
Driving design from concept through prototyping and manufacturing
Participating actively in testing, evaluation, and iterative product development
Working closely with experts across multiple disciplines including mechanics, electrochemistry, electronics, MEMS, regulatory & quality, manufacturing, and system development
Your Profile
Key qualifications for the position include:
MSc in Mechanical Engineering or similar
Expert-level SolidWorks capability, should effectively be able to teach it
Strong experience designing for manufacturing, especially injection molded parts
Strong understanding of tolerances, manufacturability, and rapid iteration
Experience with semiconductor manufacturing and MEMS structures is a strong plus
Experience with analog electronics design is a strong plus
PCB layout experience is a strong plus
We are looking for creative and analytical and structured CAD-professional who enjoys working in a highly dynamic and development environment. As a person, you are curious, problem-solving and solution-oriented, with a strong sense of ownership and accountability. You have strong execution focus as well as strong communication and collaboration skills. You enjoy testing what has been designed and believe that great products are created when top experts from different disciplines work closely together.
At Ascilion, you will have the opportunity to make an impact not only in your own area of responsibility, but also on the development of the company as a whole.
About Ascilion
Ascilion was founded in 2012 with a mission to solve the problem of sampling dermal interstitial fluid in an efficient and pain-free way. A team of engineers with deep experience in MEMS technology and microfluidics took on the challenge of solving what turned out to be a very complex problem.
We exist to bridge the worlds of precision engineering and biomarker science, creating innovative microneedle technologies that make dISF accessible, reliable, and painless; empowering researchers, clinicians, and companies to unlock the full potential of health monitoring and diagnostics.
We are currently in a very exciting expansion phase where we grow all aspects of the organization from R&D to sales. Our customer base is increasing with numerous close collaborations in Europe, the US and Asia. Come, join our journey!
To learn more about us please visit, www.ascilion.com
For more information about this position, please contact:
Krishan Johansson Haque, PhD
Sr Recruitment Consultant, QRIOS Life Science & Engineering
T: 0720701653
E: krishan.johansson-haque@qrios.se
Arbetsgivare
QRIOS AB
Vasagatan 7
11120 Stockholm
Webbplats: https://karriar.qrios.se
Ansökan
Ansök senast 3 januari (5 månader och 22 dagar kvar)
Ansök här

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