Ingenjör - Lediga jobb

När elsystemet blir allt mer komplext ökar kraven på hög datakvalitet och robusta systemstöd. I denna roll bidrar du till att utveckla och förvalta strukturerad data och datamodeller som möjliggör tillförlitliga och långsiktiga beslut för att säkerställa ett driftsäkert elsystem.

Vill du vara med och stärka Svenska kraftnäts datadrivna arbetssätt, samtidigt som du fördjupar din förståelse för det nordiska kraftsystemet? Här får du möjlighet att göra verklig skillnad i energiomställningen – där rätt data i rätt struktur är avgörande.

Om tjänsten

Som ingenjör inom data engineering och modellering bidrar du till att säkerställa att verksamhetskritiska data är korrekt, tillgänglig och långsiktigt förvaltningsbar i ett allt mer komplext elsystem. Du arbetar med modellering av kraftsystemmodeller, data management och systemstöd för driftplanering och uppföljning, samt är med och utvecklar teamets förmåga inom strukturerad datahantering. Du möjliggör ökad digitalisering och automation och bidrar till Svenska kraftnäts uppdrag i energiomställningen och utvecklingen av det nordiska kraftsystemet genom att skapa förutsättningar för datadrivenhet. I tjänsten ingår att kunna bygga och underhålla mindre script byggda med Python och C# samt att arbeta med SQL-frågor och datavyer.

Dina arbetsuppgifter:

• Modellera och vidareutveckla kraftsystemmodeller för driftplanering samt säkerställa datakvalitet genom validering och analys med användning av mindre script i C# och Python.
• Utforma och förvalta rapporter för planering och uppföljning. I detta ingår att bygga databasvyer (SQL) och att arbeta med strukturerade data i JSON och XML-format som resultat från OData-queries till REST API:er.
• Kravställa systemstöd för nätdrift, inklusive data- och informationsmodellering, test och viss konfiguration.
• Fungera som en brygga mellan elnät, data och IT genom att översätta verksamhetens behov till robusta tekniska lösningar samt etablera arbetssätt och dokumentation för dataförvaltning.

Du blir en del av enheten Nätdriftutveckling på avdelning Drift. Enheten bildades 2025 och ansvarar för att driva utvecklingsarbete för den operativa nätdriften. Här arbetar elva medarbetare med olika roller och kompetenser, bland annat verksamhetsutvecklare, processledare, produktägare och kraftsystemspecialister. Arbetet präglas av nära samarbete, kunskapsutbyte och många kontaktytor mot driftverksamheten och IT-organisationen.

Om dig

Skallkrav:

För att lyckas i rollen är du analytisk och strukturerad med förmåga att se helheter och omsätta komplex information till väl genomtänkta lösningar. Du är nyfiken och har ett intresse för att förstå och utveckla verksamheten över tid. Du trivs i samarbete med andra och bidrar aktivt i gemensamma arbetsprocesser och forum. Samtidigt är du initiativtagande och målmedveten, samt tar ansvar för att driva frågor framåt när du ser behov eller förbättringsmöjligheter.

Du ska också leva upp till https://www.statskontoret.se/forvaltningskultur/den-statliga-vardegrunden/

I denna rekrytering lägger vi stor vikt vid dina personliga egenskaper.

Du har en civilingenjörs- eller masterexamen från universitet eller högskola inom data/informationsteknologi eller motsvarande utbildning och/eller arbetslivserfarenhet som Svenska kraftnät bedömer likvärdig.

Du har även:

• Arbetslivserfarenhet inom data engineering och/eller data management, exempelvis med frågor om datakvalitet, infrastruktur eller dataanalys.
• Mycket god förmåga att kommunicera, både skriftligt och muntligt, på svenska och engelska.

Meriterande

Det är meriterande om du har:

• Kunskap om elsystemets uppbyggnad, dataflöden och tekniska beroenden.
• Erfarenhet av arbete med strukturerade data i JSON eller XML format, med Postman, REST API:er och OData eller med MSSQL-databaser.
• Erfarenhet av att dokumentera processer och strukturerade arbetssätt gällande datamodeller och informationsflöden.
• Erfarenhet av verksamhetsutveckling och/eller förvaltning av data.
• Erfarenhet av modellering av tekniska system.

Bra att veta

• Tjänsten är placerad i Sundbyberg.
• Möjlighet till distansarbete upp till 50 % #LI-hybrid.
• Resor kan förekomma någon gång per år.
• Tjänsten är en tillsvidareanställning.
• Sista ansökningsdag är den 31 augusti 2026.
• Istället för att bifoga ett personligt brev till din ansökan besvarar du ett antal frågor i ansökningsformuläret.
• I denna rekryteringsprocess tillämpas tester på slutkandidater.
• Individuell lönesättning tillämpas och sker i enlighet med de centrala löneavtalen RALS/RALS-T.
• https://www.svk.se/jobba-har/var-arbetsplats/formaner/

Vid frågor, kontakta gärna följande personer:

• Vid frågor om tjänsten: Jonas Bergman, rekryterande chef, 010 475 86 86.
• Vid frågor om rekryteringsprocessen: Linda Mattsson, ansvarig rekryterare, 010 350 91 47.
• Annika Ingeborn, facklig representant SACO, 010 475 87 72.
• Erica Midfjäll, facklig representant ST, 010 475 87 31.

Under semestertider nås vi via e-post: Förnamn.Efternamn@svk.se, och svarstiden kan under denna period vara längre än vanligt. Vi går igenom ansökningar och återkopplar om du går vidare i processen först efter sista ansökningsdag.

https://www.svk.se/jobba-har/

Vi undanber oss direktkontakt med bemannings- och rekryteringsföretag samt säljare i samband med rekrytering, vi har upphandlade avtal som gäller för Svenska kraftnät som statlig myndighet.

Övrig information

Vi ställer höga krav på våra medarbetares säkerhets- och sekretess-medvetenhet. Inför anställning genomförs säkerhetsprövning enligt säkerhetsskyddslagen (2018:585) vilket innefattar grundutredning och om anställningen avser befattning i säkerhetsklass kommer säkerhetsprövningen även att innefatta en registerkontroll. För anställning på Svenska kraftnät kan det vara ett krav på svenskt medborgarskap i vissa befattningar. Med anställningen följer en skyldighet att krigsplaceras. För mer information om personalsäkerhet på svenska kraftnät. https://www.svk.se/sakerhet-och-beredskap/sakerhetsskydd/personalsakerhet

När elsystemet blir allt mer komplext ökar kraven på hög datakvalitet och robusta systemstöd. I denna roll bidrar du till att utveckla och förvalta strukturerad data och datamodeller som möjliggör tillförlitliga och långsiktiga beslut för att säkerställa ett driftsäkert elsystem.

Vill du vara med och stärka Svenska kraftnäts datadrivna arbetssätt, samtidigt som du fördjupar din förståelse för det nordiska kraftsystemet? Här får du möjlighet att göra verklig skillnad i energiomställningen – där rätt data i rätt struktur är avgörande.

Om tjänsten

Som ingenjör inom data engineering och modellering bidrar du till att säkerställa att verksamhetskritiska data är korrekt, tillgänglig och långsiktigt förvaltningsbar i ett allt mer komplext elsystem. Du arbetar med modellering av kraftsystemmodeller, data management och systemstöd för driftplanering och uppföljning, samt är med och utvecklar teamets förmåga inom strukturerad datahantering. Du möjliggör ökad digitalisering och automation och bidrar till Svenska kraftnäts uppdrag i energiomställningen och utvecklingen av det nordiska kraftsystemet genom att skapa förutsättningar för datadrivenhet. I tjänsten ingår att kunna bygga och underhålla mindre script byggda med Python och C# samt att arbeta med SQL-frågor och datavyer.

Dina arbetsuppgifter:

• Modellera och vidareutveckla kraftsystemmodeller för driftplanering samt säkerställa datakvalitet genom validering och analys med användning av mindre script i C# och Python.
• Utforma och förvalta rapporter för planering och uppföljning. I detta ingår att bygga databasvyer (SQL) och att arbeta med strukturerade data i JSON och XML-format som resultat från OData-queries till REST API:er.
• Kravställa systemstöd för nätdrift, inklusive data- och informationsmodellering, test och viss konfiguration.
• Fungera som en brygga mellan elnät, data och IT genom att översätta verksamhetens behov till robusta tekniska lösningar samt etablera arbetssätt och dokumentation för dataförvaltning.

Du blir en del av enheten Nätdriftutveckling på avdelning Drift. Enheten bildades 2025 och ansvarar för att driva utvecklingsarbete för den operativa nätdriften. Här arbetar elva medarbetare med olika roller och kompetenser, bland annat verksamhetsutvecklare, processledare, produktägare och kraftsystemspecialister. Arbetet präglas av nära samarbete, kunskapsutbyte och många kontaktytor mot driftverksamheten och IT-organisationen.

Om dig

Skallkrav:

För att lyckas i rollen är du analytisk och strukturerad med förmåga att se helheter och omsätta komplex information till väl genomtänkta lösningar. Du är nyfiken och har ett intresse för att förstå och utveckla verksamheten över tid. Du trivs i samarbete med andra och bidrar aktivt i gemensamma arbetsprocesser och forum. Samtidigt är du initiativtagande och målmedveten, samt tar ansvar för att driva frågor framåt när du ser behov eller förbättringsmöjligheter.

Du ska också leva upp till https://www.statskontoret.se/forvaltningskultur/den-statliga-vardegrunden/

I denna rekrytering lägger vi stor vikt vid dina personliga egenskaper.

Du har en civilingenjörs- eller masterexamen från universitet eller högskola inom data/informationsteknologi eller motsvarande utbildning och/eller arbetslivserfarenhet som Svenska kraftnät bedömer likvärdig.

Du har även:

• Arbetslivserfarenhet inom data engineering och/eller data management, exempelvis med frågor om datakvalitet, infrastruktur eller dataanalys.
• Mycket god förmåga att kommunicera, både skriftligt och muntligt, på svenska och engelska.

Meriterande

Det är meriterande om du har:

• Kunskap om elsystemets uppbyggnad, dataflöden och tekniska beroenden.
• Erfarenhet av arbete med strukturerade data i JSON eller XML format, med Postman, REST API:er och OData eller med MSSQL-databaser.
• Erfarenhet av att dokumentera processer och strukturerade arbetssätt gällande datamodeller och informationsflöden.
• Erfarenhet av verksamhetsutveckling och/eller förvaltning av data.
• Erfarenhet av modellering av tekniska system.

Bra att veta

• Tjänsten är placerad i Sundbyberg.
• Möjlighet till distansarbete upp till 50 % #LI-hybrid.
• Resor kan förekomma någon gång per år.
• Tjänsten är en tillsvidareanställning.
• Sista ansökningsdag är den 31 augusti 2026.
• Istället för att bifoga ett personligt brev till din ansökan besvarar du ett antal frågor i ansökningsformuläret.
• I denna rekryteringsprocess tillämpas tester på slutkandidater.
• Individuell lönesättning tillämpas och sker i enlighet med de centrala löneavtalen RALS/RALS-T.
• https://www.svk.se/jobba-har/var-arbetsplats/formaner/

Vid frågor, kontakta gärna följande personer:

• Vid frågor om tjänsten: Jonas Bergman, rekryterande chef, 010 475 86 86.
• Vid frågor om rekryteringsprocessen: Linda Mattsson, ansvarig rekryterare, 010 350 91 47.
• Annika Ingeborn, facklig representant SACO, 010 475 87 72.
• Erica Midfjäll, facklig representant ST, 010 475 87 31.

Under semestertider nås vi via e-post: Förnamn.Efternamn@svk.se, och svarstiden kan under denna period vara längre än vanligt. Vi går igenom ansökningar och återkopplar om du går vidare i processen först efter sista ansökningsdag.

https://www.svk.se/jobba-har/

Vi undanber oss direktkontakt med bemannings- och rekryteringsföretag samt säljare i samband med rekrytering, vi har upphandlade avtal som gäller för Svenska kraftnät som statlig myndighet.

Övrig information

Vi ställer höga krav på våra medarbetares säkerhets- och sekretess-medvetenhet. Inför anställning genomförs säkerhetsprövning enligt säkerhetsskyddslagen (2018:585) vilket innefattar grundutredning och om anställningen avser befattning i säkerhetsklass kommer säkerhetsprövningen även att innefatta en registerkontroll. För anställning på Svenska kraftnät kan det vara ett krav på svenskt medborgarskap i vissa befattningar. Med anställningen följer en skyldighet att krigsplaceras. För mer information om personalsäkerhet på svenska kraftnät. https://www.svk.se/sakerhet-och-beredskap/sakerhetsskydd/personalsakerhet

Hansa Biopharma develops innovative treatments that give patients with rare and serious immune-mediated conditions a chance to a better life. We are now looking for an experienced Senior QA Manager Validation and Quality, to help shape our quality work at one of the most exciting biotech companies in the Nordics.

You will be a key player in a QA team of six dedicated colleagues, all based at our office in Lund. As Senior QA Manager, you will drive and approve validation activities - spanning process, cleaning and analytical method validation - with a clear quality perspective. You will act as subject matter expert supporting cross-functional teams, external partner management and regulatory authority inspections.

This is the right role for you if you thrive with both strategic ownership and operational presence - where one day you are reviewing validation documentation and the next you are in dialogue with a CDMO or preparing a team for an authority inspection.

• Provide strategic and operational direction for quality management and validation across development, clinical and commercial manufacturing

• QA review and approval of validation documentation

• Supplier quality management: guide and qualify external manufacturing partners (CDMOs/CMOs) throughout the product lifecycle

• Support authority inspections and internal/external audits of suppliers and vendors

• Cross-functional collaboration with CMC, Regulatory, Clinical and Supply Chain

• Drive continuous improvement of the Quality Management System (QMS) and proactively identify areas for development

We believe you are a seasoned QA professional with broad experience across both drug substance (DS) and drug product (DP) manufacturing. You are thorough and results-oriented, but also a natural collaborator who knows when to take the lead and when to seek input from others.

• Advanced degree (Ph.D. or M.Sc.) in Chemical Engineering, Chemistry, Pharmaceutical Sciences or a related discipline

• 10+ years of biopharmaceutical industry experience with a focus on QA, process development and validation

• Proven track record of leading validation activities for DS and DP through clinical and commercial stages

• Strong knowledge of aseptic manufacturing and biotechnology processes

• Deep understanding of regulatory requirements (FDA, EMA, ICH) related to manufacturing and validation

• Experience managing external partners and CDMOs/CMOs

• Experience of authority inspections (FDA, EMA) as presenter and/or coordinator

• Strong communication skills and the ability to influence across functions and organisational levels

At Hansa, you will not just have a job - you will have a role where your work directly contributes to changing lives for patients with acute and complex immune disorders.

• A close-knit, welcoming culture in a mid-sized company where you can see how your contribution makes a difference

• The opportunity to help build a fully integrated biopharmaceutical company with global reach

• Talented, driven colleagues with an open and entrepreneurial mindset

• A strong pipeline built on Hansa’s proprietary IgG-cleaving enzyme technology platform

• Office in Lund, at the heart of a vibrant Life Science ecosystem

At Hansa, we are guided by our core values: Accountability, Courage, Integrity and Pioneering. We believe in the power of diversity and are committed to building an inclusive workplace where every perspective is valued.

Send in an application as soon as possible. In this recruitment, Hansa Biopharma is collaborating with SallyQ. For questions, please contact Ellinor Crafoord, Senior Recruitment Consultant, +46793554257 or ellinor.crafoord@sallyq.se.

Vi söker dig som har en ingenjörsexamen eller motsvarande och minst fem års erfarenhet inom kvalitetssäkring av produkter och processer. Rollen innebär att säkerställa att utveckling och tillverkning följer ISO 13485, GMP och interna kvalitetsstandarder, samtidigt som förbättringsarbete och riskhantering drivs framåt.

Erfarenhet av teknisk dokumentation är central, där spårbarhet, korrekthet och fullständighet upprätthålls genom hela produktlivscykeln.

Kompetens inom avvikelsehantering behövs för att utreda orsaker, genomföra analyser och säkerställa effektiva CAPA‑åtgärder.

Rollen omfattar även granskning och bedömning av interna processer och leverantörer samt stöd vid externa revisioner för att säkerställa högsta nivå av compliance.

Du behärskar svenska och engelska obehindrat, både i tal och skrift.

Som konsult hos QRIOS Life Science & Engineering får du arbeta med spännande uppdrag inom MedTech och Pharma hos både stora och små aktörer. Här utvecklas du snabbt, och har stöd av ett erfaret QRIOS‑team i ryggen. I Malmö är vi 20+ specialister inom projektledning, kvalitet och mekanik, många med över tio års erfarenhet. Vi tror på att leverera på topp utan att kompromissa med livet utanför jobbet. Det kallar vi Work‑Life‑Passion, en kultur där både prestation och välmående får plats.

Vi söker nu fler QA-profiler inom Life Science till vårt nätverk i Stockholm/Uppsala.

Vi arbetar löpande med uppdrag hos några av regionens mest spännande läkemedels- och medicinteknikbolag – och vill nu komma i kontakt med dig som har erfarenhet av kvalitetssäkring i GMP-reglerad miljö.

Som QA Specialist arbetar du nära produktion, tekniska funktioner och projektteam för att säkerställa att processer, system och produkter uppfyller gällande regulatoriska krav.

Arbetsuppgifter kan inkludera:

• Avvikelsehantering (deviations), CAPA och change control

• Granskning och godkännande av dokumentation (SOP, batch records m.m.)

• Deltagande i audits (interna/externa)

• Stöd i kvalitetsledningssystem (QMS)

• Säkerställa efterlevnad av GMP.

• Har erfarenhet av QA inom Life Science

• Har god kunskap om GMP och regulatoriska krav

• Har arbetat med deviation/CAPA/change control

• Talar svenska och engelska flytande.

Vi arbetar både med konsultuppdrag och rekryteringar och tar gärna en dialog kring dina preferenser. Urval sker löpande och eftersom detta är en proaktiv annons så återkopplar vi så snart som möjligt.

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!

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.

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!

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

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

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!

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.

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!

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

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

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!

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

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!

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

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

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!

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

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!

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

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

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!

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.

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!

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

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se