Civilingenjör, bioteknik

Vi söker en konsult med erfarenhet av DNA-sekvenseringsmetoder och ett stort intresse för forskning och utveckling. Uppdraget är placerat i norr om Stockholm, med omgående start. Arbetsbeskrivning I denna roll kommer du att arbeta i en dynamisk och innovativ forskningsmiljö där du bidrar till att utveckla och optimera laboratoriemetoder. Dina huvudsakliga uppgifter inkluderar: Självständigt planera och genomföra experimentellt arbete i laboratoriemiljö. Bearbeta och analysera insamlade data för att dra relevanta slutsatser. Dokumentera och presentera resultat på ett tydligt och strukturerat sätt. Delta i projektmöten och bidra med din expertis i diskussioner och planering. Engagera dig i förbättringsarbete och metodutveckling inom teamet. Vem vi söker Vi letar efter en person med: Akademisk bakgrund inom Life Science, exempelvis biokemi, molekylärbiologi eller liknande ämnen. Tidigare erfarenhet av laborativt arbete inom forskning och utveckling. Gedigen kunskap om och praktisk erfarenhet av DNA-sekvenseringstekniker såsom PCR, qPCR och NGS. Förmåga att analysera komplexa data och lösa problem på ett strukturerat sätt. Goda datorkunskaper och erfarenhet av mjukvaror för dataanalys. Stark kommunikationsförmåga och vana att samarbeta med andra. Mycket goda språkkunskaper i engelska, både muntligt och skriftligt. Ansökan och process Vi hanterar ansökningar löpande, vilket innebär att tjänsten kan komma att tillsättas innan sista ansökningsdatum. Om du är intresserad av rollen, skicka in din ansökan så snart som möjligt.

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 looking to hire a Development engineer, who will act as a sub-project leader, to join the Design transfer team within the Engineering department, Technical Operations. The department’s main responsibility is to lead the industrialization of the kit manufacturing processes within the Supply Chain organization and ensuring equipment control and business continuity in the premises of our Uppsala office. The department currently consists of a total of 22 employees divided into the three individual teams: 1) Design transfer, 2) Process development & Validation and 3) Equipment & Maintenance. In this position you will act as a sub-project leader responsible for coordinating design transfer activities of new products from R&D to Supply Chain, to ensure producibility of the kit components. You will coordinate complex transfer activities and sometimes also be operational in all necessary design transfer activities such as process development, qualification and validation, manufacturing methods and article structures (BOMs etc.). You will also coordinate changes of existing products. The position is based in Uppsala and reports to Manager Design Transfer. Primary responsibilities As a Development Engineer Design Transfer your primary responsibilities includes, but is not limited to: Lead and coordinate design transfer activities in NPI and development projects according to internal quality processes. Act as change control responsible or owner by coordinating activities between other teams and departments. Lead continuous improvements and develop and improve work processes within the area. Take responsibility of identifying and implementing improvements of work processes that are connected to design transfer in NPI projects. Actively participate and contribute to performance of risk assessments of projects, processes and products. Be accountable for reporting status timely to manager and stakeholders in progress of the above. Qualifications BSc or MSc in Life Science or equivalent. Experience from a leading role in a manufacturing environment, preferably within Life science (e.g. as production preparation engineer, project manager/ activity leader). Experience from design transfer, alternatively product development, where design/ tech transfer has been included. At least 3 years relevant work experience after relevant degrees. Very good communication skills in both English and Swedish. As a person, you should have a genuine technical interest but also enjoy driving and leading projects toward challenging goals. To succeed in this role, you should have strong communication skills, be curious and creative with a proactive mindset. Finding the best solution sometimes requires being flexible and pragmatic, without loosing sight of the most important details. We are looking for a team player that always wants to find the best way of working with the aim to find the most efficient paths to deliver and reach goals. The selection process is on-going, and the position might get filled before the last day of application so please apply as soon as possible, however no later than 2025.04.06. If you want to help to deepen the understanding of real-time human biology and are looking for an exciting new challenge, we encourage you to apply!

An exciting journey to join Diamyd Medical’s own biologics manufacturing facility in Umeå. Diamyd Medical develops precision medicine therapies for Type 1 Diabetes. Diamyd® is an antigen-specific immunotherapy for the preservation of endogenous insulin production. DIAGNODE-3, a confirmatory Phase III trial is actively recruiting patients with recent-onset Type 1 Diabetes in eight European countries and has started in the US. A biomanufacturing facility is being set up in Umeå for the manufacture of recombinant GAD65, the active ingredient in the antigen-specific immunotherapy Diamyd®. In the role as Process Engineer you will work in cross-functional teams to ensure seamless integration between upstream and downstream processes and you will report to the Manufacturing Manager. Due to the nature of the job, work outside office hours will occur. Key responsibilities: Cultivate cells in shake flasks and in bioreactors. Work in cleanrooms according to cGMP regulations. Perform bioanalytical analyses. Relevant background and experience: A university degree in a relevant scientific field (e.g., pharmacy, biotechnology, bioengineering, biomedical sciences) or extensive experience in the life science industry. Several years of hands-on experience in cell cultivation. Proficiency in working with expression vector systems. Prior experience with cell cultivation in bioreactors is an advantage. Familiarity with quality-controlled environments, such as GMP or ISO-regulated industries, is beneficial. Experience working in clean room facilities is a plus. Competence in bioanalytical techniques, including electrophoresis, HPLC, Western Blot, and ELISA. Strong communication and collaboration abilities. Proficiency in both spoken and written English.

Tillsammans utvecklar vi Sahlgrenska Universitetssjukhuset för en hållbar framtid. Vi ställer om hälso- och sjukvården med målet att vara Europas ledande universitetssjukhus 2032. Tillsammans med patienterna arbetar vi för kvalitet, tillgänglighet, patientsäkerhet, forskning, utbildning och innovation – i ett sammanhållet hälso- och sjukvårdssystem i Västra Götalandsregionen. Vår vision och våra mål tar sikte mot en vård av yttersta kvalitet, där patienten alltid är i fokus. Vi erbjuder hälso- och sjukvård lokalt och regionalt, men också högspecialiserad vård till patienter i hela landet och utomlands. Våra medarbetare är vår styrka och de bidrar i kunskapsutbyten nationellt och internationellt. Med digitala verktyg och nya arbetssätt kan vi förenkla vardagen på sjukhuset och erbjuda en modern, tillgänglig och effektiv vård av högsta kvalitet. Om oss Klinisk genetik och genomik vid Sahlgrenska Universitetssjukhuset har totalt cirka 130 medarbetare, bland annat läkare, genetiska vägledare, undersköterskor, vårdadministrativ personal och biomedicinska analytiker. Centrum för Medicinsk Genomik, som ligger inom verksamheten, utför all genetisk diagnostik inom förvärvad och ärftlig cancer, fosterdiagnostik samt sällsynta sjukdomar och präglas av förändringsarbete och utveckling både avseende arbetssätt och införande av ny kunskap. Enheten för Genetisk Analys och Bioinformatik (GAB) ingår i centrumbildningen och här arbetar molekylärbiologer, sjukhusgenetiker och bioinformatiker. Efterfrågan på helgenomssekvensering ökar och NGS är ett teknikområde där utvecklingstakten är hög. Vad erbjuder vi dig Vi erbjuder dig ett spännande och utvecklande arbete med fokus på bearbetning och tolkning av avancerad genetisk data inom en verksamhet med en snabb teknisk utveckling. Arbetsuppgifter Efter introduktion och upplärning tolkar och besvarar du diagnostiska genetiska analyser med ansvar för att rätt analys blir utförd på ett patientsäkert sätt.  Du kommer att arbeta med avancerade genetiska analyser inom området för sällsynta sjukdomar. Du kommer arbeta tillsammans med tex läkare, bioinformatiker och sjukhusgenetiker och ansvara för utveckling och implementering av nya metoder i klinisk genetisk laboratoriediagnostik, ibland med en koppling till Genomic Medicine Sweden. Inom ramen för din tjänst genomgår du en utbildning till sjukhusgenetiker. Som sjukhusgenetiker har du också ett ansvar för utbildning och handledning. Du har en central roll vad gäller intern och extern kommunikation och söker kontinuerligt efter förbättrade arbetssätt, både när det gäller ny teknik/metodologi och de processer som följer det medicinska behovet.   Om dig Vi söker dig med en MSc eller civilingenjörsexamen inom biokemi/bioteknik, molekylärbiologi, genetik eller motsvarande. Du har flera års forsknings-eller arbetslivserfarenhet inom genetik och NGS och/eller helgenomssekvensering vilket inkluderar hantering av storskaliga data med viss vana av att tolka och bedöma genetiska varianter samt bearbetning av genetiska data, dokumentation och metodutveckling.  Det är meriterande om du är disputerad inom relevant ämne som till exempel genetik, biokemi, biologi och med erfarenhet av klinisk forskning eller labbverksamhet och bioinformatik.  Vi letar efter dig som är ansvarsfull och analytisk med god samarbetsförmåga och ett engagemang för utveckling. Det ställs höga krav på noggrannhet då laboratoriet är ackrediterat. Verksamheten bygger på en matrisorganisation där lyhördhet och flexibilitet är viktiga egenskaper i mötet med varierande frågeställningar, komplexa analyser och en verksamhet som är i förändring. Stor vikt kommer att läggas vid personliga egenskaper och du måste behärska svenska i tal och skrift. Välkommen med din ansökan! Möt några av våra medarbetare - Sahlgrenska Universitetssjukhuset Om Västra Götalandsregionen Västra Götalandsregionen finns till för människorna i Västra Götaland. Vi ser till att det finns god hälso- och sjukvård för alla. Vi arbetar för en hållbar utveckling och tillväxt, bra miljö, förbättrad folkhälsa, ett rikt kulturliv och goda kommunikationer i hela Västra Götaland. Västra Götalandsregionen arbetar aktivt för att digitalisera fler arbetssätt. För att vara en del av den digitala omvandlingen har du med dig grundläggande färdigheter och kan använda digitala verktyg och tjänster. Du kan söka information, kommunicera, interagera digitalt, är riskmedveten och har motivation att delta i utvecklingen för att lära nytt. Västra Götalandsregionen krigsplacerar alla tillsvidareanställda medarbetare. Vill du veta mer om Västra Götalandsregionen kan du besöka vår introduktion till nya medarbetare på länken https://www.vgregion.se/introduktion.  Du kan även läsa mer i presentation om https://mellanarkiv-offentlig.vgregion.se/alfresco/s/archive/stream/public/v1/source/available/sofia/rs4011-467070786-672/surrogate. Ansökan Västra Götalandsregionen ser helst att du registrerar din ansökan via rekryteringssystemet. Om du som sökande har frågor om den utannonserade tjänsten eller av särskilda och speciella skäl inte kan registrera dina uppgifter i ett offentligt system - kontakta kontaktperson för respektive annons. Till bemannings-, förmedlings- och rekryteringsföretag och till dig som är försäljare: Vi undanber oss vänligen men bestämt direktkontakt med bemannings-, förmedlings- och rekryteringsföretag samt andra externa aktörer och försäljare av ytterligare jobbannonser. Västra Götalandsregionen har upphandlade avtal.

Academic Resource söker nu dig som vill utveckla dina erfarenheter hos våra kunder i Life Science branschen. Vill du arbeta med något som är relevant för din utbildning och samtidigt få erfarenhet från läkemedelsindustrin eller inom bioteknik/medicinteknik? Då kanske vi har något för dig! Vi söker dig som vill arbeta som såväl Laboratorieingenjör, Laboratorietekniker, Laboratorieassistent, Processoperatör eller liknande. Vi erbjuder dig möjligheten att utvecklas inom olika områden så som produktion, QC eller QA. Du får chansen att utveckla dina laborativa och administrativa kunskaper hos välkända aktörer inom Life Science. Är du den vi söker? Exempel på arbetsuppgifter • Analysarbete inom sektionens ansvarsområde • Leverera provsvar med kort ledtid • Kontrollera att instrument och analysmetoder är fungerande och uppdaterade • Rening och kvalitetskontroller Exempel på analysmetoder som kan förekomma • PCR • HPLC, GC, Karl Fischer, BCA, Atomabsorption • ELISA, koagulationsanalyser med STA-R, Access immunoassays • GC, NIR, FTIR, titrering och våtkemiska analyser Kvalifikationer & erfarenhet Vi söker dig som har erfarenhet av laborativt arbete, antingen från utbildning eller genom tidigare anställningar. Din utbildning får gärna vara med kemisk/ biokemisk/molekylärbiologisk/BMA/biomedicinsk inriktning. Har du erfarenhet av någon av analysmetoderna ovan är det meriterande. Du har även mycket goda kunskaper i svenska och engelska i både tal och skrift, då dokumentation, metoder och instruktioner förekommer på båda språken. Är du den vi söker? Ansökan Ansök med ditt CV och personliga brev och ange referensnummer: NY1121 Kontakt [email protected] Sökord: laboratorieingenjör qc quality control analyser gmp kvalitet kontroll produktion laboratorie administration biokemi kemi molekylärbiologi hplc gc elisa bma gc nir ftir titrering våtkemi instrument pippettering kemi läkemedel industri produktion process deltid sommarjobb lediga jobb stockholm teknik assistent stockholm konsult rekrytering we take you further

Academic Resource söker nu dig som vill utveckla dina erfarenheter hos våra kunder i Life Science branschen. Vill du arbeta med något som är relevant för din utbildning och samtidigt få erfarenhet från läkemedelsindustrin eller inom bioteknik/medicinteknik? Då kanske vi har något för dig! Vi söker dig som vill arbeta som såväl Laboratorieingenjör, Laboratorietekniker, Laboratorieassistent, Processoperatör eller liknande. Vi erbjuder dig möjligheten att utvecklas inom olika områden så som produktion, QC eller QA. Du får chansen att utveckla dina laborativa och administrativa kunskaper hos välkända aktörer inom Life Science. Är du den vi söker? Exempel på arbetsuppgifter • Analysarbete inom sektionens ansvarsområde • Leverera provsvar med kort ledtid • Kontrollera att instrument och analysmetoder är fungerande och uppdaterade • Rening och kvalitetskontroller Exempel på analysmetoder som kan förekomma • PCR • HPLC, GC, Karl Fischer, BCA, Atomabsorption • ELISA, koagulationsanalyser med STA-R, Access immunoassays • GC, NIR, FTIR, titrering och våtkemiska analyser Kvalifikationer & erfarenhet Vi söker dig som har erfarenhet av laborativt arbete, antingen från utbildning eller genom tidigare anställningar. Din utbildning får gärna vara med kemisk/ biokemisk/molekylärbiologisk/BMA/biomedicinsk inriktning. Har du erfarenhet av någon av analysmetoderna ovan är det meriterande. Du har även mycket goda kunskaper i svenska och engelska i både tal och skrift, då dokumentation, metoder och instruktioner förekommer på båda språken. Är du den vi söker? Ansökan Ansök med ditt CV och personliga brev och ange referensnummer: NY1121 Kontakt [email protected] Sökord: laboratorieingenjör qc quality control analyser gmp kvalitet kontroll produktion laboratorie administration biokemi kemi molekylärbiologi hplc gc elisa bma gc nir ftir titrering våtkemi instrument pippettering kemi läkemedel industri produktion process deltid sommarjobb lediga jobb stockholm teknik assistent stockholm konsult rekrytering we take you further

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 seeking a highly motivated and experienced Scientist to join our Affinity Evaluation qPCR Section within the Highplex Department, enabling the development of new highplex products. As Scientist you will participate in research and development of product ideas and products as well as routine screening in accordance with project plans and work schedules. The position involves laboratory work, analysis and documentation. In this role you would report to the Section Manager Affinity Evaluation qPCR and be based in our Uppsala headquarters. Primary Responsibilities Actively lead and/or participate in section-, project- and department activities, and the development of product concepts and ideas. Participate as project member in meetings and project planning. Independently plan and execute laboratory work in accordance with set project plans and work schedules as well as evaluating and documenting results. Handle and prepare antibodies, antigens and biological samples for experiments. Perform PEA-experiments, mainly using qPCR as a readout. Develop new and continuously improve existing procedures, protocols and analysis methods. Perform verification studies and contribute to analyzing data shared with customers. Qualifications Ph.D. in a relevant life sciences field (e.g., Molecular Biology, Biochemistry, Biotechnology, Immunotechnology) or equivalent experience. Two or more years of working experience from an industry setting. Documented lab experience. Extensive scientific and technical knowledge in molecular biology, proteomics and biochemistry. Experience with assay development of antibody-based test methods as well as working with and optimizing PCR/qPCR and DNA sequencing (NGS). Experience of lab automation, pipetting robots and different conjugation chemistries is advantageous. Proven experience of data analysis. Experience with R and handling of large data sets is a preferable. Good general computer skills and expert level knowledge of Excel. Experience of working in, and driving projects. Good communication skills in written and spoken English, Swedish skills is a plus. Soft Skills As a person youare a team player who treats people with respect and finds it easy to communicate with others, both within the team and cross-functionally. You love to solve problems by thinking outside the box and drive development initiatives forward in cooperation with others. Finally, you are a positive person who is flexible in terms of your daily tasks. If you are a driven scientist with a passion for developing innovative protein assays and want to be part of a team at the forefront of biotechnology, we encourage you to apply. 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 on the 30th of March. The selection process is ongoing and the position could get filled before the last application date.

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 on an exciting growth trajectory, and we are thrilled to announce an opportunity for a passionate and skilled Project Manager to join our Project Management Office (PMO). Our PMO, a dedicated team of 8 project managers, spearheads the most strategic and impactful projects aligned with our visionary goals. As a Project Manager at Olink, part of Thermo Fisher Scientific, you will be at the forefront of innovation in proteomics, driving a variety of projects including New Product Introductions (NPI) and diverse business initiatives. Your role will be pivotal in ensuring the continued success and advancement of our cutting-edge products. This position is based at our Uppsala office and reports directly to the Head of PMO. If you are ready to make a significant impact and contribute to the future of proteomics, we would love to hear from you! Primary Responsibilities As Project Manager you will be responsible for leading and delivering strategic projects according to set timeframe and budget. This could include, but is not limited to, the following tasks: Develop a timetable for the projects according to set goals. Lead projects towards agreed goals according to set schedule, quality and budget. Collaborate with project stakeholders internally and externally. Responsible for communication with the Steering Committee. Continually work to improve, educate and lead within Olink's project processes. Develop, manage and drive improvements through engagement, support teamwork and apply structured models in project management. Qualifications/skills Relevant degree in a related field (Bsc, MSc, PhD in Engineering, Life Sciences) Certification in Project Management (e.g PMP, IPMA etc) is highly beneficial. At least a few years of experience in project management or product management within the Life Science industry. Experience of NPI projects is highly advantageous. Professional proficiency in both Swedish and English is mandatory and necessary to be successful in this role. As a person you are responsive, curious and committed. You are a solution-focused leader who thrives in a dynamic and fast-paced environment. Furthermore, you are a team player who is good at communicating with different stakeholders and who can see things from different perspectives. To be successful in this role you should also be pragmatic and meticulous when needed and be able to see things from a long-term, strategic perspective. The selection process is on-going, and the position might get filled before the last day of application so please apply as soon as possible, however no later than 2025.03.30. If you want to help to deepen the understanding of real-time human biology and are looking for an exciting new challenge, we encourage you to apply!

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 now looking for a Development Engineer to join the Assay Development NGS team within the Highplex department, RnD. If you want to work with a world-leading technology that contributes to the development of precision medicine, you might be the person we are looking for. Assay Development NGS has the main responsibility to develop immunoassays for the Olink Highplex products and to evaluate assay performance throughput development projects. This includes performing verification experiments and generating assay performance data for website. Product development is carried out in projects with members from other departments. Further more, Assay Development NGS also contributes to research and development of product concepts and ideas. Assay Development NGS currently consists of 10 people, but since the company is growing rapidly with very exciting things going on, the group needs to be expanded with additional members. Primary Responsibilities As a Development Engineer in the group, your duties will vary across project phases. It will consist of both laboratory work, but also data analysis and logging of information. The main tasks will be to: Perform experiments using Olinks PEA (Proximity Extension Assay) with NGS as a readout platform. Plan and perform laboratory work in accordance with set project plans and work schedules. Evaluate, report and document results from the laboratory work according to existing procedures. Handle and register data for large amounts of antibodies, antigens and biological samples. Actively participate in the development of the group's and department's activities and participate in improvement projects. Qualifications/skills Master’s degree in life sciences or corresponding education. Documented lab experience and a few years of working experience from the industry. Experience in pipetting small volumes and of using pipetting robots is advantageous. Experience with antibody-based test methods as well as with PCR and NGS. Experience with handling and characterizing biological samples, with a focus on plasma and serum is advantageous. Good computer skills in general and good knowledge of Excel. Experience of using python or R-scripts are advantageous. Experience of working in projects. Fluent in spoken and written English, Swedish is a plus. As a person you are responsible, driven, proactive and solution oriented. As we handle large amounts of reagents and data, we value that you are thorough and structured. You are a team player who finds it easy to communicate and interact with others both within the group and with those who work in other departments and functions. It is important that you have a positive attitude and can adapt to changing circumstances. The selection process is on-going, and the position might get filled before the last day of application so please apply as soon as possible, however no later than 2025.03.23.. If you want to help to deepen the understanding of real-time human biology and are looking for an exciting new challenge, we encourage you to apply!

NorthX Biologics is a Contract Development and Manufacturing Organization that offers services and support in the development and manufacturing of biologics used as vaccines, gene therapy and other advanced applications. We have a long tradition of pharmaceutical manufacturing and have been manufacturing biologics to GMP since 1992. In 2021 we were recognised as a national innovation hub for advanced therapeutics and have expanded our development capabilities. This includes a new development organisation with cutting edge laboratories and technologies. We are now searching a talented Process Development Scientist with a passion for bioprocesses, bacterial fermentation and protein purification with a genuine enjoyment of both hands-on lab work and analytical tasks. As a Process Development Scientist, you will play a key role in developing and optimizing processes for recombinant production of biologicals for vaccines and advanced therapeutics. You will be supporting client and internal programs to achieve scalable and high yielding workflows, suitable for clinical production of. Tasks include planning and execution of experiments in the lab as well as reporting and contributing to deliveries from the project teams as a subject matter expert within your area.  You will also be involved in the preparation and execution of GMP batches for clinical use. As you will be part of the entire process from gene to active ingredient you are technically skilled in fermentation and/or protein purification. Experiences in pharmaceutical development and GMP production are meriting, but for the right person and combination of skills. We believe that an academic level of MSc or PhD within a relevant field (Biotechnology, Biochemistry, Biology, Chemistry) is a good base to be successful in the position. The candidate we are seeking has current knowledge about modern technologies and methods within biotechnological production. Your curiosity and desire to expand your expertise to various disciplines are highly valued. We are working in cross functional teams where individuals contribute to both upstream and downstream work but depending on the profile of the successful candidate the focus of the role can be adjusted towards a specific area. Technical skills Required Highly meriting Bacterial cultivation and recombinant expression Tangential flow filtration Chromatographic purification of proteins, DNA and/or mRNA High throughput screening Basic molecular biology methods (AGE, PCR, cloning) Design of experiments Basic microbiology CDMO experience and GMP manufacturing Biochemical analysis (SDS-PAGE, Western Blot, UV/Vis)   The nature of the position is a mix of hands-on work in the laboratory, documenting and writing tasks. You are self-motivated and demonstrate high levels of creativity in finding solutions to complex challenges. The NorthX working climate is highly collaborative and you are expected to bring a positive force to the team and be prepared to assist where needed. You communicate professionally with internal and external parts, your intrapersonal skills and experience to work in teams will be highly valued. Applicants must be able to demonstrate strong written and verbal communication skills and be fluent in English. NorthX Biologics is an expanding company within an exciting field, working with customers and projects globally. For the right candidate we are offering a position with strong opportunities for personal development. NorthX Biologics is located in Matfors, 4 h north of Stockholm, with a 15 min commute to the city of Sundsvall. Housing in the area is affordable and availability of rentals with immediate access is high. NorthX values the work-life-balance for employees and offers flexibility in planning your workdays and hours. The city and area offer a high quality of life through closeness to nature, a vast variety of activities on snow, water and land and a city center rich in restaurants, history, and cultural events.   For further information, please contact:   Agnes Zimmer, Head of Process Development                    [email protected] Akademikerna, Lina Kejerhag                                                   [email protected] Unionen, Jan-Anders Atterhagen                                             [email protected]