Civilingenjör, bioteknik

Göteborgs universitet möter samhällets utmaningar med mångsidig kunskap. 56 000 studenter och 6 600 medarbetare gör universitetet till en stor och inspirerande arbetsplats. Stark forskning och attraktiva utbildningar lockar forskare och studenter från hela världen. Med ny kunskap och nya perspektiv bidrar Göteborgs universitet till en bättre framtid.På institutionen för biomedicin bedrivs forskning och undervisning inom prekliniska och kliniska medicinska ämnen. Institutionen är indelad i följande fyra avdelningar: infektionssjukdomar, mikrobiologi och immunologi, medicinsk kemi och cellbiologi samt laboratoriemedicin. För närvarande har institutionen cirka 340 medarbetare och cirka 450 Mkr i omsättning. Anställningen som biträdande forskare kommer att ligga under avdelning för Laboratoriemedicin/ sektionen Klinisk genetik och genomik. Forskargruppen har en multidisciplinär sammansättning av molekylärbiologer, ingenjörer, BMA och bioinformatiker inom såväl akademin som sjukvården. Forskargruppen har ett tätt samarbete med läkare vid Sahlgrenska sjukhuset, såsom barnonkologer, patologer, kirurger. Tillsammans arbetar gruppen för att identifiera cancergener och undersöka de onkogenetiska cellulära mekanismerna som driver tumörutveckling och progression av hjärntumörer hos barn. Hos barn spelar fusionsgener (sammanfogning av två gener) en viktig roll vid tumörbildning och dessa utgör attraktiva mål för riktad behandling men är också viktiga för diagnostik. Gruppen arbetar för att föra in ny metodologi och kunskap i klinisk rutin för förbättrad tumörklassificering och vägledning av behandling för barncancerpatienter och har också ett nära nationellt samarbete inom ”Genomic Medicine Sweden” (GMS) barncancer projektet. Arbetsuppgifter  Arbetsuppgifterna kommer främst att vara laborativa och innefatta genetisk analys av DNA och RNA från patientprover med ”long-read sekvensering” (t.ex. ONT/nanopore, PacBio/SMRT), alternativt optical genome mapping, samt funktionell analys av genetiska fynd via cellodlingsförsök (såsom transfektion, CRISPR/Cas9, proliferationsassay, proteinextraktion, Western blot och immunfluorescens). Vidare innefattar arbetet bioinformatik, och dataanalys. Vi förutsätter att du självständigt kan planera, genomföra och sammanställa resultat från molekylärgenetiska analyser och in vitro-experiment. Tillsammans med övrig personal i gruppen kommer du att hämta/samla in, hantera och organisera prover från patienter i forskningsbiobanken. Vi förväntar oss därför att du har god samarbetsförmåga och gillar att arbeta i team. Kvalifikationer  Behörig är sökande som har en  civilingenjörsexamen i Bioteknik eller mastersexamen (MSc) i molekylärbiologi/biomedicin/medicin, eller motsvarande. Praktiska och teoretiska kunskaper inom humangenetik och tumörbiologi är ett krav. Praktisk och analytisk erfarenhet av Next generation sequencing eller long-read metoder är meriterande. Tidigare laberfarenhet inom experimentell cellbiologi såsom cellodling och in vitro-experiment (t.ex. transfektion, CRISPR/Cas9, Western blot, immunfärgning) är mycket meriterande. Önskvärt är erfarenhet av arbete med dataanalys i miljöerna R, Python och MatLab. Arbetet kommer att ställa krav på självständighet och god analytisk förmåga. Den sökande ska vara ansvarskännande och noggrann. Eftersom vi publicerar våra resultat i internationella tidskrifter bör du behärska engelska i tal och skrift. Tyngdpunkt läggs vid tidigare erfarenheter och personlig lämplighet.  Anställning  Anställningen är på heltid och tidsbegränsad, 6 månader, med placering tills vidare på institutionen för biomedicin. Tillträde sker enligt överenskommelse.  Kontaktuppgifter för anställningen  Har du frågor om anställningen är du välkommen att kontakta Sjukhusgenetiker, Forskare, Docent: Frida Abel. Mejl: [email protected] Telefonnummer: +46 76- 828 00 96  Fackliga organisationer  Fackliga företrädare vid Göteborgs universitet hittar du här: https://www.gu.se/om-universitetet/jobba-hos-oss/hjalp-for-sokande  Ansökan  Du söker anställningen via Göteborgs universitets rekryteringsportal genom att klicka på knappen "Ansök". Du som sökande ansvarar för att ansökan är komplett i enlighet med annonsen och att den är universitetet tillhanda senast sista ansökningsdag.  Ansökan ska vara inkommen senast: 2025-07-09 Universitetet arbetar aktivt för en arbetsmiljö med jämställda förhållanden och sätter värde på de kvalitéer mångfald tillför verksamheten. Universitetet tillämpar individuell lönesättning. Enligt Riksarkivets föreskrifter är universitetet skyldigt att förvara ansökningshandlingar i två år efter tillsättningsbeslutet. Om du som sökande till en anställning särskilt begär tillbaka dina handlingar återsänds de när de två åren har förflutit, i annat fall kommer de att gallras ut. Till bemannings- och rekryteringsföretag och till dig som är försäljare: Göteborgs universitet anlitar upphandlad annonsbyrå i samband med rekrytering av personal. Vi undanber oss vänligen men bestämt direktkontakt med bemannings- och rekryteringsföretag samt försäljare av jobbannonser.

At Procella Therapeutics, we are developing first-in-class allogeneic regenerative medicines with clinical indications ranging from advanced heart failure to Parkinson’s disease as well as in-house cGMP manufacturing capabilities to advance our portfolio of novel therapies to the clinic. We are now looking for a Bioprocessing Scientist to join our team. As a Bioprocessing Scientist you will work in the process development group, proposing the scientific direction of ongoing work and supporting/executing associated wet lab activities to deliver on project objectives. In this role, you will be working closely with other colleagues in an agile, multidisciplinary environment, to deliver innovative cell therapies and/or novel technology solutions to accelerate the translation of cell therapies to clinic. The Scientist may be tasked with performing process development, QC testing, product manufacturing, or analytical method development depending on the prevailing project goals of the company. Key responsibilities Your contributions and responsibilities will be: • Drive the scientific direction of various projects by proposing development strategies, designing experiments, coordinating teams and planning of ongoing labwork. • Delivery of project objectives on time, on budget, and to a suitable level of quality to meet project milestones, including participating in daily labwork. • Preparation of data reports and present data to internal or external stakeholders. • Routine laboratory and equipment maintenance operations, including cleaning of lab areas and equipment, correct use and maintenance of lab equipment, ensuring availability of raw materials and consumables and support for overall inventory and budget management. • Drafting of SOPs and performing training of staff. • Keeping abreast of latest scientific and industry developments and using this knowledge to inform development capabilities and direction within the team, to support the growth of SmartCella’s portfolio. Required qualifications and competence We believe you need to have: • PhD in a relevant subject area, or BSc and/or MSc in a relevant subject area with 2+ years’ relevant work experience. • Several years of prior practical experience working in cell and gene therapy. • Knowledge and understanding of bioreactors, bioprocessing equipment, media exchange/advanced filtration, cell sorting, Fill&Finish. • Experience with Quality by Design methodology, and Design of Experiments (DoE). • Proficient in use of MS Office tools. • Fluent in written and spoken English and have excellent interpersonal and communication skills, both written and verbal. • Experience working under biosafety conditions and using aseptic technique. It will be a merit if you also have: • Prior experience with relevant analytical methods such as flow cytometry, spectroscopy, qPCR, or ddPCR. • Cell and gene therapy product development in an industry setting. • Experience working with pluripotent stem cells and familiarity with developmental biology. • Innovative and entrepreneurial mindset. • Working under a quality management system. • Familiarity with Lean, Six Sigma, or similar methodologies. • Knowledge and understanding of using risk-based approaches for process assessments. • Established understanding of using statistical and data analysis techniques. • Skills in software programming languages. Interested? Submit your application today! We will review applications on an ongoing basis and hope to fill the position as soon as possible. SmartCella is a world-leading biotech company pioneering the future of targeted therapies by combining first-in-class delivery platforms with cutting-edge cell and gene therapies. The SmartCella group consist of SmartCella Holding AB, ProCella Therapeutics AB, SmartWise AB and SmartCella Solutions AB with a total of 82 employees from more than 20 nationalities.

Lunds universitet grundades 1666 och rankas återkommande som ett av världens främsta lärosäten. Här finns omkring 47 000 studenter och mer än 8 800 medarbetare i Lund, Helsingborg och Malmö. Vi förenas i vår strävan att förstå, förklara och förbättra vår värld och människors villkor. Lunds universitet välkomnar sökande med olika bakgrund och erfarenheter. Jämställdhet, lika villkor och mångfald är grundläggande principer för alla delar av vår verksamhet. Arbetsplatsen Institutionen för Immunteknologi bedriver forskning inom livsvetenskaperna såsom immunologi, onkologi, och överkänslighet/allergi. De moderna lokalerna är belägna på Medicon Village där akademisk forskning bedrivs sida vid sida med privata företag och aktörer från sjukvårdssektorn. En rad viktiga infrastrukturer finns tillgängliga här, bland annat speciallaboratorier för spatial omik, masspektrometri, flödescytometri och antikroppsframställning, samt NBIS (National Bioinformatics Infrastructure Sweden). Tillämpningen av avancerade tekniker för att lösa komplexa biomedicinska utmaningar har bidragit till att institutionen ligger i framkant i flera forskningsområden och ett flertal spin-off bolag är också verksamma på Medicon Village. Vi erbjuder Lunds universitet är en statlig myndighet vilket innebär att du får särskilda förmåner, generös semester och en förmånlig tjänstepension. Läs mer på universitetets webbplats om att vara anställd hos oss https://www.lu.se/om-universitetet/jobba-hos-oss Arbetsuppgifter Du kommer ingå i en translationell forskargrupp som studerar tumörmikromiljön, med särskilt fokus på lymfom.  Du kommer vara ansvarig för att praktiskt utföra laborativa moment såsom infärgning av tumörvävnad och molekylär profilering (protein, RNA, DNA) av patientprover. Arbetsuppgifterna innefattar även analys av genererade data såsom bildanalys, och bioinformatiska arbetsflöden. Projektet är fokuserat på att identifiera och vidareutveckla möjliga nya terapeutiska och prognostiska markör Kvalifikationer Du som söker har: - Magisterexamen i bioteknik, cellbiologi, molekylärbiologi eller motsvarande. - Praktisk erfarenhet av bioinformatik, såsom att t.ex. applicera R skript. - Utmärkta kunskaper och förmågor i engelska i både skrift och tal. - Utmärkta samarbets- och kommunikativa förmågor. Meriterande för tjänsten är - Praktisk erfarenhet av att hantera vävnad och/eller humana celler - Praktisk erfarenhet av att arbeta med protein och/eller RNA-relaterade laborativa flöden. - Praktisk erfarenhet av att färga in vävnad för multiplex immunofluorescence-medierad bildanalys. - Erfarenhet av att arbeta med QuPath - Erfarenhet av att arbeta med dataanalys av patientmaterial och statistisk utvärdering - Kunskap inom lymfombiologi, cancerbiologi och/eller immunologi Personliga egenskaper, såsom driv, intresse för forskning, noggrannhet, god kommunikativ- och samarbetsförmåga, är av särskild vikt. Villkor 10 månaders projektanställning med start den 11 augusti eller enl överenskommelse, dock ej senare än 31 augusti. Instruktioner för ansökan Ansökan bör innehålla personligt brev med motivering till varför du är intresserad av anställningen och på vilket sätt dina meriter matchar anställningen. Ansökan bör även innehålla CV, utbildningsbetyg eller motsvarande samt övrigt som du önskar åberopa (kopior av betyg, uppgifter till referenser, rekommendationsbrev etc.). Universitetet tillämpar individuell lönesättning. Ange gärna löneanspråk i din ansökan. LTH – Lunds Tekniska Högskola – är den tekniska fakulteten vid Lunds universitet. På LTH utbildar vi människor, bygger kunskap för framtiden och arbetar hårt för att utveckla samhället. Vi skapar utrymme för briljant forskning och inspirerar till kreativ utveckling av teknik, arkitektur och design. Här läser närmare 10 000 studenter. Varje år publicerar våra forskare – varav många verkar inom världsledande profilområden – omkring 100 avhandlingar och 2 000 vetenskapliga rön. En rad forskningsresultat och studentarbeten förädlas till innovationer. Tillsammans utforskar och skapar vi – till nytta för världen. Vi undanber oss alla kontakter från annonsförsäljare, rekryterings- och bemanningsföretag på grund av statliga upphandlingsregler.

Who we are Olink, part of Thermo Fisher Scientific, is transforming the understanding of human diseases through advanced proteomics. We are driven by a commitment to innovation, quality, and transparency, providing exceptional solutions and support for human protein biomarker discovery. For many years, the critical role of proteins in human biology has been recognized, but technological constraints limited comprehensive research into their potential across various biological processes and diseases. With our innovative Olink solutions, scientists can now measure thousands of human proteins simultaneously using just a few microliters of blood. Our highly specific and validated assays cover a wide dynamic range, empowering groundbreaking research. Our services include flexible protein biomarker solutions, with a robust library of thoroughly validated assays covering ~5000 proteins. As we expand globally, we continue to play a pivotal role in shaping the future of scientific discovery. To learn more, visit www.olink.com.  Position Description: We are currently seeking a Laboratory Coordinator for our Analysis Service (AS) department in Uppsala. Analysis Service is our service laboratory, analyzing customer samples using Olink products in compliance with applicable GXP requirements (e.g. GCP) and ISO17025. AS consists of three units: The Laboratory unit, the Laboratory Operations unit and the Quality unit. The role as Laboratory Coordinator belongs to Laboratory Operations unit. The main task as the role of Laboratory Coordinator is to prepare and coordinate various activities within the department, e.g. purchasing, logistics, supply and reagents. You will work in close communication with both the Laboratory unit and the functions that exist in its surroundings. You will strive to minimize the laboratory downtime and improve the laboratory’s work environment, and act as an important point of contact for the laboratory and other departments. Primary Responsibilities: Control of reagents and supply, orders, and forecasting of consumables and reagents. Coordinate activities concerning e.g. reagents, supplies and logistics with other departments, such as Analysis Service US, Supply Chain, Facility, Finance and IT. Support the Analysis Service team to work efficiently, safely and with the highest possible quality. Coordinate Access management within Analysis service, e.g. train staff who need access to our facilities. Independent work according to Olink QMS instructions. Work independently within the Analysis Service team and collaborate effectively with other teams to ensure alignment of global Olink processes. Qualifications/Skills: BSc within the Life Science field or similar. 3+ years of experience working in a laboratory setting with customer deliveries (internal or external) and the ability to meet strict deadlines. Familiarity with GCP regulations in laboratory work. Experience with LIMS or similar systems is an advantage. Experience with ERP or similar systems is an advantage. Experience with logistics work is and advantage. Fluent verbal and written communications skills in English. We are looking for a meticulous and quality-focused professional who enjoys driving their own daily tasks as well as coordinating communication and activities between different functions within the department/company. You are pro-active, flexible, and capable of adjusting your priorities in a fast-paced and dynamic environment. You are a team player with strong communication skills and a positive, solution-oriented mindset. Please note that you should already be eligible to work in Sweden and should be able to come into our Uppsala office daily. Please submit your resume and a cover letter detailing your relevant experience and why you are the ideal candidate for this position. The last application date is the 19th of June 2025. If this sounds interesting, please send us your application, and come join Olink!

Xbrane Biopharma AB is a pioneering Swedish biotech company dedicated to delivering high-quality biosimilar drugs—affordable alternatives to existing biologic therapies. We have an exciting opportunity for you to join Xbrane Biopharma as a Senior Analytical Manager. Xbrane is actively exploring strategic expansion opportunities, and as part of our team, you’ll play a role in shaping how we grow our presence in the global biosimilar market and venture into new areas. About the Role Xbrane Biopharma is seeking an experienced and motivated Senior Manager in late stage analytics to join our Analytical Science and Technology (ASAT) team with a focus on cell-based assays. In this role, you’ll be responsible for coordinating QC activities, including method validation, transfers and stability studies. You’ll contribute by your expertise to support Xbrane’s development programs and collaborate closely with Contract Manufacturing Organizations (CMOs). This is a great opportunity to be part of a cross-functional and fast-paced environment where your work will play a key role in bringing high-quality biologics to patients worldwide. Key Responsibilities • Lead the planning, coordination, and tracking of timelines and costs for both internal and external activities to ensure CMO progress aligns with overall project plans. • Serve as the primary point of contact for day-to-day QC activities at CMOs, ensuring alignment with project timelines and deliverables. • Act as a Subject Matter Expert (SME) in analytical sciences with expertise cell-based potency assays, and binding assays. • Support CMOs in managing and investigating deviations, changes, CAPAs, and out-of-specification (OOS) results. • Lead the validation and technology transfer of analytical methods, as well as stability studies and other analytical work within cross-functional teams. • Provide technical support, troubleshooting, and review for analytical activities, as well as contribute to regulatory submissions. Your profile • University degree in Life Sciences (e.g., Biotechnology, Biochemistry, Pharmacy). • Expert in cell-based potency assays and binding assays for biopharmaceuticals • Proven track record from method development, validation, analytical tech transfer, and stability studies • Experience from working at QC or as QA- with analytical focus during development and/or commercial production • Proven track record supporting program in commercial phase and development programs in clinical phases • Proven experience in managing CMO/CLO relationships and external activities. You are highly organized with strong time-management abilities. A collaborative team player, you demonstrate excellent communication, presentation, and writing skills, and are fluent in English. You naturally build and maintain productive relationships with colleagues and external partners, fostering a culture of open communication and effective collaboration. Why choose Xbrane? Xbrane Biopharma is a values-driven and certified Great Place to Work® that offers opportunities for professional growth, influence, and development in a people-focused environment. If you have a can-do attitude and on top of that share our values; — Make it happen, Beat yesterday, Nothing is Impossible, and We win as one, you will thrive together with us. We believe that when you thrive, so does our impact. That’s why we offer a benefits package designed to support your well-being, both in and outside of work. Interested? In this recruitment, Xbrane Biopharma is collaborating with Mpya Sci & Tech. Please submit your application at www.mpyascitech.com no later than the 10th of August. We are conducting an ongoing selection process, so don't delay your application, as the position may be filled before the final application date. Questions? Please contact Johan Östman at +46(0)76 628 78 91 or [email protected] Xbrane Biopharma is a Swedish biotechnology company that develops and manufactures biosimilars. We’re proud to be a Great Place to Work® certified company, where innovation, collaboration, and an entrepreneurial mindset are at the heart of everything we do. Our vision and business concept are closely aligned with global sustainability and contribute to achieving the UN Sustainable Development Goals No. 3 – Good Health and Well-being, and No. 10 – Reduced Inequalities. Xbrane’s headquarters are located at the vibrant Solna Campus just outside Stockholm, offering a collaborative and inspiring work environment. Please visit www.xbrane.com for more information.

Xbrane Biopharma AB is a pioneering Swedish biotech company dedicated to delivering high-quality biosimilar drugs—affordable alternatives to existing biologic therapies. We have an exciting opportunity for you to join Xbrane Biopharma as Drug Product Manufacturing Manager to work closely with our partners and external manufacturers. Xbrane is actively exploring strategic opportunities for expansion, and as part of our team, you’ll play a role in shaping how we grow our presence in the global biosimilar market and venture into new areas. About the Role Xbrane Biopharma is looking for an experienced and motivated Drug Product Manufacturing Manager to join our Manufacturing Science and Technology (MSAT) team. In this role, you will be responsible for coordinating drug product manufacturing activities, including process transfers, manufacturing campaigns, and process validation. You will contribute your expertise to support Xbrane’s development programs and collaborate closely with Contract Manufacturing Organizations (CMOs). This is a great opportunity to be part of a cross-functional and fast-paced environment where your work will play a key role in bringing high-quality biologics to patients worldwide. Key Responsibilities • Leading the planning, coordination, and follow-up of timelines and costs for internal and external activities to ensure progress at CMOs aligns with project plans. • Supporting drug product manufacturing activities through all development phases, from early clinical to commercial supply. • Providing technical support including documentation preparation and review, troubleshooting, investigations, and input to regulatory submissions. • Acting as a Subject Matter Expert (SME) in drug product manufacturing, ideally with experience in fill-finish operations and sterile manufacturing processes. Your profile We are looking for an experienced Drug Product Specialist with great communication and negotiating skills, and a proactive approach, who contributes to an efficient and engaging work environment. • A university degree in Life Sciences (e.g., Biotechnology, Biochemistry, Pharmacy). • Extensive experience in the biopharmaceutical industry, with a strong background in drug product manufacturing. • Proven track record supporting development programs across clinical and commercial phases, including technology transfer and process validation. • Deep understanding of cGMP requirements for drug product manufacturing. • Demonstrated ability to manage external activities and maintaining strong relationships with CMOs. • Excellent communication skills and fluency in English, both written and spoken. • You have a natural way of creating and maintaining productive relationships with colleagues and external contacts where collaboration and communication are in focus. • Experience with aseptic/sterile manufacturing and knowledge of container-closure systems is a strong advantage. Why choose Xbrane Biopharma? Xbrane Biopharma is a values-driven and certified Great Place to Work® that offers opportunities for professional growth, influence, and development in a people-focused environment. If you have a can-do attitude and on top of that share our values; — Make it happen, Beat yesterday, Nothing is Impossible, and We win as one, you will thrive together with us. We believe that when you thrive, so does our impact. That’s why we offer a benefits package designed to support your well-being, both in and outside of work. Interested? In this recruitment, Xbrane Biopharma is collaborating with Mpya Sci & Tech. Please submit your application at www.mpyascitech.com no later than the 10th of August. We are conducting an ongoing selection process. Questions?Please contact Perjohan Säfström at +46(0)76 163 57 00, [email protected] or Linnéa Andersson at +46(0)72 888 65 77, [email protected]. Xbrane Biopharma is a Swedish biotechnology company that develops and manufactures biosimilars. We’re proud to be a Great Place to Work® certified company, where innovation, collaboration, and an entrepreneurial mindset are at the heart of everything we do. Our vision and business concept are closely aligned with global sustainability and contribute to achieving the UN Sustainable Development Goals No. 3 – Good Health and Well-being, and No. 10 – Reduced Inequalities. Xbrane’s headquarters are located at the vibrant Solna Campus just outside Stockholm, offering a collaborative and inspiring work environment. Please visit www.xbrane.com for more information.

Xbrane Biopharma AB is a pioneering Swedish biotech company dedicated to delivering high-quality biosimilar drugs—affordable alternatives to existing biologic therapies. We have an exciting opportunity for you to join Xbrane Biopharma as Drug Substance Manufacturing Manager to work closely with our partners and external manufacturers. Xbrane is actively exploring strategic opportunities for expansion, and as part of our team, you’ll play a role in shaping how we grow our presence in the global biosimilar market and venture into new areas. About the Role Xbrane Biopharma is looking for an experienced and motivated Drug Substance Manufacturing Manager, preferrable with experience from upstream processes, to join our Manufacturing Science and Technology (MSAT) team. In this role, you will be responsible for coordinating drug substance manufacturing activities, including process transfers, manufacturing campaigns, and validation work. You will also bring your expertise to support Xbrane’s development programs and work closely with Contract Manufacturing Organizations (CMOs). This is a great opportunity to be part of a cross-functional and fast-paced environment where your work will play a key role in bringing high-quality biologics to patients worldwide. Key Responsibilities • Leading the planning, coordination, and follow-up of timelines and costs for internal and external activities to ensure progress at CMOs is aligned with project plans. • Supporting manufacturing through all phases of development, from early clinical to commercial. • Providing technical support such as documentation preparation and review, troubleshooting, investigations, and contributions to regulatory submissions. • Acting as a Subject Matter Expert (SME) in drug substance manufacturing, with a focus on upstream processes. Your profile We are looking for an experienced Drug Substance Specialist with great communication and negotiating skills, and a proactive approach, who contributes to an efficient and engaging work environment. • A university degree in Life Sciences (e.g., Biotechnology, Biochemistry, Biology). • Extensive experience in the biopharmaceutical industry, particularly in biologics drug substance manufacturing. • Proven track record across several development phases including process development, clinical supply, and commercial manufacturing. • Deep understanding of cGMP requirements for DS manufacturing. • Demonstrated ability to manage external activities and maintaining strong working relationships with CMOs. • Excellent communication skills and fluency in English, both written and spoken. • You have a natural way of creating and maintaining productive relationships with colleagues and external contacts where collaboration and communication are in focus. • Experience with the establishment and testing of cell banks is a strong advantage. Why choose Xbrane Biopharma? Xbrane Biopharma is a values-driven and certified Great Place to Work® that offers opportunities for professional growth, influence, and development in a people-focused environment. If you have a can-do attitude and on top of that share our values; — Make it happen, Beat yesterday, Nothing is Impossible, and We win as one, you will thrive together with us. We believe that when you thrive, so does our impact. That’s why we offer a benefits package designed to support your well-being, both in and outside of work. Interested? In this recruitment, Xbrane Biopharma is collaborating with Mpya Sci & Tech. Please submit your application at www.mpyascitech.com no later than the 10th of August. We are conducting an ongoing selection process, so don't delay your application, as the position may be filled before the final application date. Questions? Please contact Perjohan Säfström at +46(0)76 163 57 00, [email protected] or Linnéa Andersson at +46(0)72 888 65 77, [email protected]. Xbrane Biopharma is a Swedish biotechnology company that develops and manufactures biosimilars. We’re proud to be a Great Place to Work® certified company, where innovation, collaboration, and an entrepreneurial mindset are at the heart of everything we do. Our vision and business concept are closely aligned with global sustainability and contribute to achieving the UN Sustainable Development Goals No. 3 – Good Health and Well-being, and No. 10 – Reduced Inequalities. Xbrane’s headquarters are located at the vibrant Solna Campus just outside Stockholm, offering a collaborative and inspiring work environment. Please visit www.xbrane.com for more information.

Gör skillnad. Varje dag. Vill du vara med och utveckla framtidens avancerade terapier? Advanced Therapy Medicinal Products (ATMP) centrum vid Skånes universitetssjukhus (Sus) i Lund växer och nu söker vi en GMP-ingenjör eller anläggningstekniker som vill bidra till att bygga upp och driva vår moderna GMP-infrastruktur för tillverkning av avancerade läkemedel. ATMP-centrum är en nysatsning inom Region Skåne för att möjliggöra produktion av avancerade terapier som genterapi, cellterapi och vävnadstekniska produkter inom sjukhusets väggar. Vi arbetar i nära samarbete med forskare, kliniker och läkemedelsutvecklare för att möjliggöra kliniska prövningar och framtida behandlingar. Vi befinner oss i ett uppbyggnadsskede och söker nu dig som vill vara en del av denna spännande resa. Centrumet har i uppdrag att tillverka, bereda och koordinera kliniska prövningar med ATMP samt vara ett stöd till akademi och företag som i regionen vill genomföra kliniska prövningar med denna typ av läkemedel. Region Skåne har precis slutfört byggnationen av en GMP-facilitet på Skånes universitetssjukhus i Lund som tillhör ATMP-centrum. GMP-faciliteten innehåller renrum för tillverkning och beredning av ATMP. Valideringen av lokalerna är genomförd och nu förbereds den första tillverkningen av cellbaserade läkemedel. ATMP-centrum kommer också att vara en del av sjukhusapoteksfunktionen och bereda såväl marknadsgodkända ATMP som prövningsläkemedel. ARBETSUPPGIFTER Som GMP-ingenjör är du en nyckelperson i arbetet med att säkerställa att vår anläggning uppfyller kraven enligt GMP (Good Manufacturing Practice). Du kommer arbeta med kvalificering, validering, dokumentation och tekniskt stöd i nära samverkan med kvalitetsansvariga och tillverkningsteamet. Du kommer också att vara delaktig i utvecklingsarbetet med nya tillverkningsmetoder. Exempel på arbetsuppgifter: •Ansvara för drift, övervakning och underhåll av renrumsanläggningar och teknisk utrustning. •Medverka i validerings- och kvalificeringsarbete (t.ex. IQ/OQ/PQ). •Upprätta dokument och följa rutiner enligt GMP. •Delta i riskanalyser och avvikelserapporter. •Bidra till kontinuerliga förbättringar och utveckling av anläggningen. •Medverka i utvecklingen av nya tillverkningsprocesser. I ditt arbete hos oss kommer du att behöva ta mycket eget ansvar då det är en verksamhet under uppbyggnad. Du kommer att få en utvecklande och stimulerande arbetsmiljö samt utbildning anpassad efter verksamheten. Slutligen kommer du att ingå i en positiv grupp med hög kompetens och ett visionärt ledarskap. KVALIFIKATIONER Vi söker dig som har: •Ingenjörsexamen inom medicinsk biologi, bioteknik, kemiteknik eller motsvarande område. •Erfarenhet av arbete i GMP-reglerad verksamhet, exempelvis inom läkemedelsproduktion, medicinteknik eller kvalitetsarbete. •God teknisk förståelse och vana vid teknisk dokumentation. •Flytande svenska i tal och skrift samt god engelska. Erfarenhet av arbete med renrum eller tillverkning av ATMP-produkter samt erfarenhet av kvalificering och validering enligt GMP är meriterande. Då vi är en liten verksamhet som är under uppbyggnad är det viktigt att du är flexibel, har mycket god samarbetsförmåga samt är villig att hjälpa till där det behövs. Du ska ha förmåga att ta egna initiativ och självständigt kunna utföra ditt arbete. Vi värdesätter att du är kvalitetsmedveten, noggrann, har god samarbetsförmåga och är prestigelös. Stor vikt kommer läggas vid personlig lämplighet. I denna rekrytering använder vi oss av löpande urval. Varmt välkommen med din ansökan redan idag! ÖVRIGT Region Skåne ansvarar för hälso- och sjukvård, kollektivtrafik och en hållbar utveckling i hela Skåne. Vårt högsta beslutande organ är regionfullmäktige, som väljs direkt av invånarna i Skåne. Region Skåne är en värderingsstyrd organisation som arbetar med värderingarna välkomnande, drivande, omtanke och respekt i allt vi gör. Skånes universitetssjukhus (Sus) finns i Lund och Malmö och är landets tredje största sjukhus. Sus är ett kunskapsnav för hälso- och sjukvård i livets alla skeden på regional, nationell och internationell nivå. Våra 12 000 medarbetare är med och driver utvecklingen inom universitetssjukhusets tre uppdragsområden: vård, forskning och utbildning. Hos oss får du arbeta i en värderingsstyrd organisation som utvecklar hälso- och sjukvården tillsammans med patienter och deras närstående. Välkommen! På https://www.skane.se/ledigajobb kan du se i vilket skede Region Skånes rekryteringar befinner sig och hur många som har sökt tjänsterna. Till bemannings- och rekryteringsföretag och till dig som är försäljare: Vi undanber oss vänligen men bestämt direktkontakt med bemannings- och rekryteringsföretag samt försäljare av ytterligare jobbannonser.

At Intervacc, we are pioneering the next generation of veterinary vaccines through our proprietary technology platform. Rooted in research from the Karolinska Institutet (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 a CMC Regulatory Affairs Manager who will be responsible for the CMC regulatory strategy and execution for the company’s marketed products, in additions to supporting the development and commercialization of new vaccine products. The CMC Regulatory Affairs Manager will have a central role in providing guidance, support, and technical expertise for CMC activities and related regulatory initiatives. You will work with different markets to fulfil 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 Regulatory Affairs Manager, you will provide CMC regulatory strategy input and expertise for our marketed and investigational products to ensure the company’s products are developed and maintained in compliance with global regulatory requirements and guidance. Duties and responsibilities include: • Prepare, review, and submit CMC regulatory documents throughout the product lifecycle • Develop and implement CMC regulatory strategies to support clinical development, registration, and post-approval changes • Act as the primary CMC regulatory contact with health authorities, internal teams, and external partners • Oversee change control processes and ensure timely reporting of CMC variations and updates • Tracking of all regulatory activities and housekeeping of the filed documentation • Maintain 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 in a science-related subject e.g. pharmacy, biology or chemistry • CMC Regulatory Affairs experience with submissions for biologics or biotechnology-derived products e.g. vaccines • Knowledge of the drug development process for biologics (including upstream and downstream processes and analytical methods) and regulatory submissions • Knowledge of current regulatory CMC requirements • 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: • Is analytical, solution-oriented with a strong personal drive • Is structured and organized but also adaptable to change • Has a good eye for detail and a thorough approach to work • Is a proactive, flexible, motivated and ambitious team player If you are ready to bring your expertise in CMC Regulatory Affairs, 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 Institutet (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: [email protected]

About Bioextrax Bioextrax is an innovation-driven company using industrial biotechnology to contribute to a more sustainable future. We are originally a spin-off from the Department of Biotechnology at Lund University and are now a rapidly growing publicly traded company. Our vision is to be a world-leader in bio-based technologies accelerating the transition to a sustainable, green global economy. The company is consistently working to develop innovative and green solutions based on microbiology and biotechnology. The core of our business is a bio-based platform technology for hydrolysis of protein rich materials. This technology has many applications that can contribute to a bio-based and circular economy. We have developed methods to produce the bio-based and biodegradable polymers polyhydroxyalkanoates (PHAs) and to turn various protein-rich materials such as poultry feathers into valuable materials to be used in feed, textile, and cosmetic applications. While we are bringing our technologies to the market, we are constantly exploring new ways our platform can contribute to a more sustainable society. Does this interest you? Are you up for the challenge? About the position We are looking for a Biotechnology Engineer to join our team in Lund, Sweden. You will be working closely with our Chief Technology Officer in a creative role where your tasks will range from design and execution of lab/pilot experiments, to exploration of new applications of our bio-based technologies. You will be working in a team developing and identifying new bio-based processes, and the evaluation and testing of strategies to improve bioprocess KPIs such as yields and product properties. You will have an essential role in designing experiments, running bench-top and pilot-scale fermentations and downstream processing. The work will focus on improving KPIs, generating and analyzing data and materials for customers, preparing experimental reports, and providing input on technical approaches to meet project goals. The position will require occasional shift work (e.g. evenings, nights and/or weekends). Job responsibilities: - Independent and in-team design and operation of lab and pilot experiments - Presentation and interpretation of results and projects outcomes, standard operating protocols, SOP. - Support Bioextrax management team in communication customer interaction. Who are you? We are looking for an ambitious individual with an MSc or BSc degree in Chemical engineering, Biotechnology, Microbiology or a related field. The candidate should be excited about the prospect of joining a quickly expanding team on our journey to become a global leader within the biobased economy. Required lab experience: - Cultivation and characterization of pure microbial strains in lab scale bioreactors - Optimization of microbial cultivation media for high-cell density growth and high product yield - Downstream processing of microbial metabolites - Characterization of intracellular and exocellular microbial products - Online/Offline monitoring of microbial growth and products (spectroscopy, electrophoresis and chromatography) Desirable experience: - Pilot-scale fermentation - Biomass pre-treatments - Bioprocess cost estimation - Statistical optimization of media for microbial cultivations - Cell-free hydrolase reactions (e.g., protease, esterase, amylase, lipase, or cellulase) About you: You have an entrepreneurial mindset and the ability to take advantage of new opportunities and let go of things that do not work. You also possess a willingness to learn new things, collaborate, and critically assess new ideas. We think that the right person can work on a stand-alone basis. It is also important that you are flexible, solution-oriented, innovative and at the same time being reliable. You possess good social skills and are a down-to-earth team player.