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Vill du arbeta nära forskning och utveckling i en högteknologisk miljö där ditt arbete gör verklig skillnad? Nu söker vi en vikarierande forskningsassistent till vårt agglomereringslaboratorium i Malmberget. Framtidens viktigaste jobb Vi vill leda omställningen av vår industri mot en hållbar framtid. På samma sätt som vi villförändra världen, vill vi utveckla alla som är med oss på resan, personligt och professionellt. Vill duvara med och forma framtiden för världens gruv- och mineralindustri? Din roll Som forskningsassistent i Agglomereringslaboratoriet har du en varierad och praktisk roll där du bidrar till LKAB:s utveckling av både produkter och processer. I labbet arbetar vi med att tillverka och analysera råkulor och pellets med hjälp av avancerad utrustning. Arbetet spänner över flera skalor – från mikro- och labbskala till pilotskala – och du får arbeta med olika metoder och instrument. Du registrerar prover och rapporterar analysresultat i vårt labbdatasystem samt arbetar nära forskare, tekniker och labingenjörer. Exempel på arbetsuppgifter: Tillverka råkulor genom mikrorullning och analysera deras produktegenskaper Utföra analyser i partikellaboratoriet Underhålla och rengöra laboratorieutrustning Registrera och rapportera analysdata Arbetet är till stor del praktiskt och innefattar även vissa administrativa moment. Tunga arbetsmoment förekommer. Det här har du med dig Du är en strukturerad och ansvarstagande person som trivs i en roll där du planerar och driver ditt arbete framåt enligt givna instruktioner. Du har lätt för att samarbeta och bidrar till ett gott arbetsklimat, samtidigt som du tar stort ansvar för att arbetet utförs noggrant, särskilt då rollen innefattar hantering av data och analysresultat. Utöver det förväntar vi oss att du har Gymnasieutbildning, gärna med inriktning mot natur eller teknik B-körkort Goda kunskaper i svenska och engelska, i tal och skrift Det är meriterande om du även har Erfarenhet från processindustrin eller laboratorieverksamhet Varmt välkommen med din ansökan! Vi strävar efter en rättvis och objektiv rekryteringsprocess. Därför ber vi vanligtvis inte om personliga brev. I stället ber vi dig att svara på frågor relaterat till den specifika tjänsten du söker. Dina svar hjälper oss att förstå din kompetens och erfarenhet, så ta dig tid att svara så tydligt och utförligt som möjligt. Vi går snart in i semestertider och vill därför informera om att rekryteringsprocessen kommer att ta ett sommaruppehåll. Sista ansökningsdag för den här rollen är den 5 augusti och vi återkommer med återkoppling i slutet av augusti. Ansökningar kan komma att behandlas löpande, innan sista ansökningsdag. Tack för ditt intresse och vi ser fram emot att läsa din ansökan och önskar dig en riktigt fin sommar! Start: Enligt överenskommelse. Plats: Malmberget Omfattning: Heltid, dagtid. Visstidsanställning till sommaren 2027 Kontakt: För mer information om tjänsten är du välkommen att kontakta rekryterande chef Lotta Hedström lotta.hedstrom@lkab.com Facklig kontakt: IF Metall Gruv 4:an (Malmberget), Tomas Larsson Thomas.L.Larsson@lkab.com LKAB är en internationell gruv- och mineralkoncern med norra Sverige som bas och hela världen som arbetsplats. Vileder vägen mot koldioxidfri produktion och vi gör det tillsammans – i en öppen, varm och säker arbetsmiljö medteknologi och utveckling i fokus. Vi välkomnar utmaningar, innovativa idéer och initiativförmåga, alltid medjämställdhet och mångfald i fokus.
Nu har du chansen att bli en av oss! Vi arbetar tillsammans med hjärta och kvalitet för att kunna ge bästa möjliga service till Ronneby kommuns invånare. Ronneby ligger vackert mellan hav och skog i mitten av Blekinge. Dessutom har vi bra kommunikationer med bil, tåg och flyg. Dina 2500 blivande kollegor är duktiga på att möta framtidens utmaningar och våra invånares ökade förväntningar genom digitalisering, samarbete och ett engagerat ledarskap. Tillsammans med dig gör vi Ronneby ännu bättre! Läs om Ronneby kommun via https://ronneby.se/naringsliv--arbete/arbeta-hos-oss.html Utbildningsförvaltningen i Ronneby har satt fokus på det kollegiala lärandet! Verksamheten ska genomsyras av kollegialt lärande och de metoder som bygger på vetenskaplig grund och beprövad erfarenhet. Då når vi framgång! Hos oss ska samtliga medarbetare vara väl medvetna om våra styrkor och värna om dessa, samtidigt som vi hela tiden utvecklas. Det gör vi tillsammans! I utbildningsförvaltningen arbetar vi efter den ”röda tråden”, en gemensam syn på utveckling och lärande med demokratisk värdegrund från förskola, grundskola, anpassad skola till gymnasie- och vuxenutbildning. Ta chansen att jobba i en kommun som fokuserar på kärnan i utbildningen! 1 plats(er). ARBETSUPPGIFTER I ditt uppdrag som musiklärare ingår det att planera, genomföra och utvärdera det pedagogiska arbetet. Du ska även hitta strategier för att nå varje enskild elev och stärka denne i sin kunskapsutveckling. Tillsammans med övriga kollegor ska du ha skolans värdegrund och kunskapssyn i fokus. Ett aktivt värdegrundsarbete är en självklarhet för dig. Du har drivkraft och bidrar till skolans kvalitetsarbete. Du kommer att undervisa elever från Saxemaraskolan åk 3-6 samt elever på Hobyskolan åk 3-6. Undervisningen sker på Hobyskolan. Tjänsten är på 60%. I din roll är du delaktig för att skapa en trygg grund för våra elever. En viktigt del i arbetet är att stimulera och motivera eleverna att utveckla sina förmågor och skapa möjligheter för lärande. Du ska vara väl förtrogen med skolan styrdokument och insatt i dess dokumentationskrav. KVALIFIKATIONER Du ska ha en lärarlegitimation. Annan person som innehar pedagogisk utbildning som arbetsgivaren bedömer likvärdig, kan vara aktuell men då för en visstidsanställning. Du ska vara en person som har lätt för att skapa goda relationer med eleverna där du kommer att ansvara fullt ut för musikundervisningen. Du ska kunna uttrycka dig väl i tal och skrift. Du ska kunna kommunicera och samarbeta med kollegor, elever, vårdnadshavare samt övriga professioner du möter i ditt yrke. Du bör ha grundläggande kunskaper i office365 samt relevanta system för tjänsten. Vi ser det meriterande att du har arbetat som musiklärare tidigare och att du behärskar olika instrument. Innan tillsättning sker krävs enligt lag uppvisande av ett giltigt utdrag ur polisens belastningsregister. https://polisen.se/tjanster-tillstand/belastningsregistret/skola-eller-forskola/ Löneform: Månadslön. Anställningsform: Tillsvidareanställning. Varaktighet: Tillsvidare. Observera att Ronneby kommun har tagit bort det personliga brevet från ansökningsprocessen. Du som söker en tjänst hos oss kommer istället i ansökningsförfarandet att få svara på ett antal frågor där du beskriver din kompetens inom efterfrågat område. I urvalsarbetet kommer vi att utgå ifrån dessa svar som komplement till ditt CV, och alltså inte begära in ett personligt brev. I de fall det finns lagkrav på utdrag ur belastningsregistret kommer du att behöva uppvisa ett sådant. För vissa tjänster i Ronneby kommun genomför vi bakgrundskontroller av slutkandidater. Hos oss i Ronneby kommun omfattas våra medarbetare av centrala kollektivavtal (HÖK och AB). Vi tillämpar individuell och differentierad lönesättning, och erbjuder ersättningar enligt kollektivavtalens bestämmelser. Via länken kan du läsa om lönestatistik i Ronneby kommun. https://ronneby.se/naringsliv--arbete/arbeta-hos-oss/lediga-jobb-hos-ronneby-kommun.html Vårt lönepolitiska arbete bygger på de centrala kollektivavtalen. Har du frågor är du välkommen att kontakta Personalenheten via personal@ronneby.se. För att kvalitetssäkra rekryteringsprocessen samt möjliggöra god kommunikation med dig som sökande ber vi dig ansöka via ansökningslänken i annonsen.
Lyten Sweden is seeking a professional Quality Control Technician to join our R&D organization in Västerås. In this role you will be responsible for analysing materials, incoming parts, product intermediates and finalized products for R&D, production and external suppliers using a wide range of instruments. You will participates in problem solving, technical troubleshooting exercises and technical discussions where needed. Key responsibilities (including but not limited to) Write the testing plans for materials, incoming parts, product intermediates and finalized products Perform testing of control plan inspection items using a variety of laboratory instruments Perform data analysis/interpretation and report according to quality standards Be able to troubleshoot first of line problems arising on the instruments Drive method improvements; help update standard operating procedures as needed Perform regular (daily, weekly, monthly) preventive maintenance on instruments Become familiar with the fundamentals of quality assurance and quality control principles and relevant quality management system requirements (control plan, non-conformity management, deviation and change management, control samples and control charts, calibration management, ISO9001, IATF16949, ISO17025, etc.) Adhere to and ensure 5S and safety protocols are maintained within the laboratory work environment Always work with safety as first priority Requirements Qualifications and experience Bachelor´s degree (or technical school degree) in Chemistry or a technical field is preferred. Significant relevant previous laboratory and work experience. Hands-on experience using a set of relevant analytical instruments and measurement equipment. Experience within a quality control work environment is a plus. Curious, technically educated, and with an interest in a laboratory career in industry. Knowledgeable in Lean and six sigma Familiar with SPC, FMEA, Quality troubleshooting tools and problem-solving methodology Specific skills Excellent oral and written communication skills in English, Swedish is a plus User experience with Office and JIRA software
SHL Medical is a world-leading provider in the design, development, and manufacturing of advanced self-injection devices. With a global team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to deliver innovative autoinjectors, pen injectors, and other drug delivery systems that ensure effective treatment for patients. Headquartered in Switzerland since 2018, with key operations in Sweden, Taiwan, and the US, we are united by a commitment to innovation, impact, and growth. Together, we empower our people to develop solutions that make a meaningful difference in the lives of millions of patients while fostering a supportive, inclusive, and dynamic workplace for our colleagues. Job Overview The Sr Quality Engineer is responsible for acting as Workstream Lead Quality (QE Lead) in the Design & Development projects as responsible for design assurance activities across all project phases ensuring quality and robustness of the product design and manufacturing processes (including product care projects, design changes and design reviews). Furthermore, the Quality representative is responsible to assure compliance with applicable regulations and SHL Medical AB’s Quality Management System (QMS) in both Design & Development Projects and other Quality element tasks such as CAPAs and Change Control handling. Main Responsibilities Maintain and calibrate laboratory equipment and instruments to ensure operational reliability and compliance. To act as Workstream Lead Quality applying Quality Engineering principles in a dynamic way in development and production projects. To represent Workstream Lead Quality in all Design Controls and Product Development related aspects. To ensure that all design control and production/process control projects meet applicable (local and international) regulations, Corporate, Customer, and Local QMS requirements. To utilize Quality Engineering best practices, ensuring internal and external customers’ needs and requirements are built into new products and future product changes. To support SMEs in the identification and traceability of Critical to Quality attributes by applying Advanced Product Quality Planning/DFSS/Risk tools and techniques across all product development phases. To promote the use of statistics in testing and control of quality. To support and guide Risk Management activities (FMEAs). To assess and approve the risk mitigation techniques implemented and whether these are consistent with the product classification, potential defect types, defect frequency, severity, patient risk, process capability, product and process controls. To support Device product/process development and production activities, including the following: Develop or review product/process specifications and requirements. Develop or review product reliability specifications/predictions, and reliability test activities. To develop quality plans and work further with Manufacturing on the transfer of quality requirements. To contribute to compilation and maintenance of Design History Files (DHF). Minimum requirements Minimum 5+ years' work experience in relevant roles such as Quality Assurance, Quality Engineering Fluent in written and spoken English. Experience from working with interpretation of ISO Standards, e.g EN ISO 14971:2019 and EN ISO 13485:2016 Experience in establishing, reviewing and approving quality documentation Experience with model development, test method validation and statistical analysis. Green Belt practitioner, or demonstrated experience in application of Quality Methodologies such as DFSS, DMAIC, Lean Hands-on experience in product development from ideation to launch in the Medical Device Industry Preferred Qualifications Fluent in written and spoken Swedish. Experience with Design Controls and Design Transfer activities within the Medical Device industry Experience with injection molding and automated assembly manufacturing processes. Familiarity with validation activities including IQ/OQ/PQ and Test Method Validation (TMV). Experience working in cross-functional and international environments. We Offer Challenging assignments in a fast-growing and innovative industry. An exciting opportunity in a fast-growing international medical technology company. A modern working environment with multicultural and dynamic teams. A centrally located office in Zug, very close to the train station. Interested in joining SHL Medical and in supporting us with your expertise and personality? Then we look forward to receiving your application to our Talent Acquisition Department. Please note: We do not accept applications from recruitment agencies for this position
Aimpoint AB is the company that invented and developed the red dot sight, for which we are today the world-leading provider. Aimpoint sights are used in the civilian hunting and shooting markets, as well as by police and military forces. The company has over 570 employees and a turnover of approximately 2,3 billion SEK. Sales in the United States are managed through our American subsidiary, Aimpoint Inc. Our headquarters are located in Malmö, with production facilities in Malmö and Gällivare. Aimpoint is part of the Sandberg Development group. For more information about the company, please visit www.aimpoint.com/se TEST ENGINEER Are you looking for a workplace where innovation, curiosity, and teamwork drive us forward? We invite you to join us on our journey as a experienced Test Engineer within Aimpoint’s Advanced and System Verification Engineering team—a role where curiosity meets precision and hands-on ingenuity. Your Role As a Test Engineer, you’ll be a key player in planning, coordinating, evaluating and verifying advanced products in the fields of optics, electronics, mechanics, and environmental testing. You will not only perform thorough tests and document the results with high accuracy but also write test plans, develop new test methods and innovative equipment solutions to ensure we meet industry-leading standards. What you will do · Act as a test and verification resource within an agile, cross‑functional team, supporting sprint planning, execution, reviews, and retrospectives. · Test lead: planning, coordinating and conducting tests, verifications, and analyses within optics, electronics, mechanics and environmental systems. · Being the team’s key competence in test activities by driving test planning, stakeholder alignment, prioritization, and follow-up of test execution and results. · Continuously prioritize and adapt test activities based on team needs, development progress, and risk assessments. · Documenting findings in clear, precise technical reports in both English and Swedish. · Developing and validating new testing methods and equipment. · Maintaining and improving laboratory tools and instruments. · Collaborating closely with stakeholders to ensure products meet stringent quality criteria. · Exploring creative, hands-on solutions—perfect for someone who enjoys tinkering and practical hobby projects. Your Profile We are looking for someone with a strong technical background who thrives in an innovative environment and enjoys both problem-solving and collaboration. Skills and Experience · Experience with documentation management and report writing—particularly technical English. · Ability to collaborate closely with multidisciplinary team members and take shared responsibility for team deliveries and quality outcomes. Personal Qualities · A flexible, social, and communicative approach, with an eagerness to adapt to varied tasks and challenges. · Naturally curious about science and technology, with special interest in optics and physics. · Creativity and a passion for hands-on work—someone who enjoys experimenting and building. Meritorious · Experience with mechanical CAD software (SolidWorks) · Programming experience (C# / Python, MATLAB, C/C++) · Experience of working as a contributing resource in agile or iterative development teams (e.g. Scrum, Kanban, or similar ways of working). · Knowledge in optics, electronics, and chemistry. · Previous experience in risk management and military test standards. Education and Qualifications A degree in Engineering (Physics, Electrical, Mechanical, Computer Engineering) or equivalent experience. At least 5 years of experience in product development in physics, mechanics, electronics or equivalent. The salary range for an Test Engingeer is SEK 45,000–55,000 depending on experience and qualifications. Why Aimpoint? We are driven by our core values: Performance, Innovation, and Commitment! - and we believe you are too! Just like us, you enjoy having fun at work and find interaction with others both challenging and rewarding. Collaboration with colleagues and customers is a natural part of the job. You can apply quickly and easily through our career page. Questions? Feel free to contact P&C Sr Recruiting Specialist, Sofie Selind, at: sofie.selind@aimpoint.com Applications will be reviewed on an ongoing basis - so don’t delay! Learn more about us and how we handle your personal data on our website. Important Information At Aimpoint security is a key factor and due to this, we perform a background check on all positions within the company before employment.
Company description: At NKT in Karlskrona, we develop and manufacture high voltage power cables that enable the transition to renewable energy. Here, you will be part of an international engineering centre with advanced high voltage test halls, modern cable production and the cable laying vessel NKT Victoria. As Connectors, we collaborate to develop innovative technology that connects a greener and more sustainable world. NKT is headquartered in Denmark and operates in more than 30 countries.NKT - We connect a greener world. www.NKT.com. Job description:We are looking for a Laboratory Engineer for the department Material Technology in KarlskronaNKT connects a greener world with high-quality power cable technology and plays a central role in the global transition to renewable energy. At our factory in Karlskrona, we design, develop and manufacture high-voltage power cable solutions that enable a sustainable future. We are now looking for a Laboratory Engineer to join our Material Technology department, a role where you will combine laboratory work with a key responsibility for our digital lab environment. Shape the future of our laboratory systemsAs a Laboratory Engineer at NKT, you will not only contribute with reliable and accurate test results, you will also take on a central role in developing, maintaining and supporting our Laboratory Information Management System (LIMS). You will act as a link between laboratory users, instruments and system suppliers, ensuring that our systems support the business in an efficient and sustainable way. This is a broad and diverse role where you work both operationally and strategically. Main resnonsibilities: Plan, perform and report laboratory work according to applicable standards and instructions Quality control of incoming material and quality assurance of manufacturing steps Operate and maintain laboratory equipment Develop, adapt and improve the LIMS environment based on business need Identify and resolve issues across system, instruments and workflows Act as main point of contact towards system suppliers and support improvements Provide user support and training in LIMS to ensure efficient daily use Handle system administration and ensure stable system performance Who are you?You are an organized and structured colleague who enjoys working both practically in the lab and with digital tools and systems. You are curious, solution-oriented and take initiative to improve ways of working.You thrive in a role where you collaborate broadly, support colleagues and manage of both processes and systems. Key requirements: Bachelor’s degree in engineering, chemistry, physics – or equivalent experience Good communication skills in Swedish and English, both spoken and written Experience or interest in working with databases and digital systems Structured, service-minded and comfortable supporting users Contact and applicationNKT is committed to fostering a diverse organization and an inclusive culture where people from different backgrounds can thrive and perform at their best. You will gain exciting opportunities for career development and attractive benefits. Read more about our offer and listen to some voices of NKT Connectors here! We will review applications continuously, but we recommend you apply no later than 2026-08-09. An extract from the criminal record, alcohol and drug tests, along with personality and capacity tests, might be part of our recruitment process. If you have any questions about the role or the recruitment process, please reach out to Agnes Carlsson, agnes.carlsson@nkt.com. Please note that due to the GDPR regulations we cannot accept any applications via e-mail. Due to the holiday season, we kindly ask for your understanding that our response times may be slightly longer than usual. We collect confidential candidate experience feedback to improve our recruitment process. Your responses are for quality development only and do not affect hiring decisions. Union representativesSveriges Ingenjörer – Christian Fisch, +46 455 56 380Unionen – Joakim Wikström, +46 734 070 243Ledarna – Roger Jönsson, +46 455 55 911 Be a Connector of the green tomorrow! #LI-AC2 #LI-Onsite
Är du legitimerad biomedicinsk analytiker eller undersköterska och söker en varierande och stimulerande tjänst med patientkontakt och omväxlande arbetsuppgifter? Då kan Akutlaboratoriet på Karlskoga lasarett vara rätt arbetsplats för dig! Vi är ett team på 23 medarbetare med bred kompetens och varierande erfarenheter. Tillsammans skapar vi en arbetsmiljö som präglas av samarbete, engagemang och trivsel. Vår verksamhet omfattar Klinisk kemi, Transfusionsmedicin, provtagning samt blod- och plasmatappning. Verksamheten inom klinisk kemi och transfusionsmedicin bedrivs dygnet runt. Laboratoriets provtagning tar emot patienter vardagar dagtid för venös- eller kapillär provtagning samt belastningar. På laboratoriet roterar du mellan olika arbetsstationer utifrån dina behörigheter, vilket skapar stor variation i arbetsuppgifterna och ger dig möjlighet att utveckla en bred kompetens. Vi erbjuder också goda möjligheter till fördjupning och kompetensutveckling inom våra olika verksamhetsområden. Arbetsuppgifter Som biomedicinsk analytiker hos oss arbetar du självständigt med laborativt arbete. Dina huvudsakliga arbetsuppgifter innefattar analys, bedömning och tekniskt godkännande av prover inom områdena klinisk kemi, immunokemi, hematologi, koagulation, PNA och transfusionsmedicin. Vi har även en provtagningsmottagning där du utför både venösa och kapillära provtagningar på patienter. Som undersköterska arbetar du på laboratoriets provtagning med venös- och kapillär provtagning samt belastningar. Beställning av förbrukningsmaterial samt viss provhantering kan också ingå i arbetsuppgifterna. Kvalifikationer Vi söker dig som är legitimerad biomedicinsk analytiker eller undersköterska. Du har lätt för att samarbeta med andra och ger ett positivt och respektfullt bemötande mot både kollegor och patienter. Du kan arbeta både självständigt och i team, är ansvarstagande och flexibel. Du har god prioriteringsförmåga även i stressade situationer. Du är kvalitetsmedveten och bidrar aktivt till verksamhetens utveckling. Det är viktigt att tycker om att arbeta med patienter och att du har goda kunskaper i svenska, både i tal och i skrift. Eftersom laboratoriet bemannas dygnet runt, alla årets dagar, förväntas du som biomedicinsk analytiker vara flexibel och villig att arbeta enligt ett skiftande schema. Tidigare erfarenhet av laborativt arbete är meriterande. Vi fäster stor vikt vid personliga egenskaper som gott bemötande, ansvarskänsla, samarbetsförmåga och kvalitetsmedvetenhet. Ansökan Ansökan ska innehålla CV och personligt brev. Intyg, betyg, examensbevis med mera ska lämnas vid en eventuell intervju. Om du är eller tidigare varit anställd i Region Örebro län kommer vi ta interna referenser från din nuvarande eller tidigare chef, om du blir aktuell för anställning. Kontroll av registerutdrag från Polismyndigheten kan komma att ske enligt aktuell lagstiftning. Som anställd i Region Örebro län omfattas du av trygga kollektivavtal. Läs mer om villkor och förmåner. Vi sätter löner individuellt och differentierat. Läs mer om lön och lönestatistik. Vi krigsplacerar våra tillsvidareanställda och i vissa fall även visstidsanställda. Läs mer om vad det innebär. Om verksamheten Laboratorieverksamheten i Region Örebro län är en länsklinik, vilket innebär ett samlat ansvar för den laboratoriemedicinska service som bedrivs vid laboratorierna inom Universitetssjukhuset Örebro, Karlskoga lasarett och Lindesberg lasarett. Vi driver en bred verksamhet inom områdena klinisk kemi, bakteriologi, virologi, immunologi, transfusionsmedicin inklusive terapeutisk plasmaferesbehandling, patologi, genetik, cytologi, molekylärgenetik och verksamhet för instrumentsterilisering. Här arbetar närmare 300 personer med rutindiagnostik, forskning och utveckling samt utbildning. Region Örebro län är en av länets största arbetsgivare och en viktig tillväxtmotor i regionen. Vi arbetar för människors hälsa, trygghet och välbefinnande och för länets utveckling. Hos oss finns spännande och viktiga jobb inom bland annat hälso- och sjukvård, tandvård, kollektivtrafik, kultur och näringslivsutveckling. Övrig information Välkommen med din ansökan! Vi har gjort vårt medieval för denna rekrytering och undanber oss därför erbjudanden om annonserings- och rekryteringshjälp i samband med denna annonsering.
The European Spallation Source (ESS) will soon be the world’s most powerful source of neutrons, providing researchers with unique opportunities to explore the structure of materials at the atomic level. Neutron scattering at ESS will address critical questions in physics, chemistry, geology, materials science and life science. About the role: The Scientific Support Division at ESS is looking for a Biodeuteration Scientist to support the ESS neutron user program. The Deuteration group at ESS operates a support service providing deuterium-labelled samples for the scientific users of the ESS neutron instruments for carrying out a broad range of experiments primarily in materials and life science research. In this position, you will play an important role in ensuring the success of biological and biomaterial experiments at ESS by further developing methods for the biological production of a range of deuterated biomolecules, contributing deuterated materials for user proposals and requested by ESS users, and optimising purification and analysis capabilities. In the ESS Deuteration group, we also work in close collaboration with our international colleques at other deuteration laboratories. In this role, you will: Provide deuteration services for neutron experiment users, including the production, purification and characterization of a variety of biologically deuterated molecules. Further develop ESS capabilities for biodeuteration as well as related purification and analysis methods, in order to meet the evolving needs of the ESS scientific user program. Coordinate the planning, organization and operation of ESS biodeuteration support including proposal calls, feasibility reviews and proposal work scheduling. Maintain and operate the biological deuteration facilities of ESS in collaboration with the Lund Protein Production Facility at Lund University hosting our biodeuteration activities. Supervise and provide technical guidance to visitors and hosted students and postdocs working on biodeuteration projects. Participate in external and internal collaborations to enhance ESS biodeuteration capabilities and scientific output of the user programme. Disseminate results and method developments through publications in peer-reviewed journals and at relevant scientific meetings as appropriate. Collaborate with Deuteration laboratories at other large-scale research infrastructure to to ensure continuing development of Deuteration services ESS. This is a full-time permanent position based at the brand new https://www.youtube.com/watch?v=d5h4bIEfM5Q About you: We're seeking an experienced and highly motivated biochemist/biologist with a PhD in biology, molecular biology, biochemistry or biotechnology and a strong track record of the expression of biological molecules in microbial cell cultures for research. You have experience of bacterial and yeast expression systems and biochemical modifications and purification methodologies. In addition to designing biological production processes and optimising purification methods, you also bring deep expertise and understanding of modern cell culturing and analytical techniques - including automated fermentation systems, purification technologies and biophysical characterisation methods. Experience in protein ligation-mediated polypeptide engineering, and/or genetic engineering of microbial expression systems is an advantage. You take pride in delivering reliable results on time, and you thrive in both independent and collaborative settings. Comfortable working with colleagues and neutron users from many disciplines, you have a service-minded proactive approach and an eagerness to contribute to a fast-paced, international research environment. Communicating clearly in English - both written and spoken - comes naturally to you, and you're confident engaging with colleagues from a wide range of technical backgrounds and presenting your work at conferences. If you’ve worked with biological deuteration previously, that’s a strong advantage. So is experience operating automated bioreactor systems, experience with higher eukaryotic cell culturing, biomolecule production and purification at mg-g scale, or supporting user-driven custom projects in research, infrastructure or contract environments. You’re someone who wants to contribute to the bigger picture outside your own lab work – both scientifically but also practically by acting as a driver for the development of new capabilities, maintaining high safety standards, caring for shared infrastructure, and keeping instruments in top condition. Most importantly, you bring curiosity, scientific rigour, and a team-oriented spirit to everything you do. To apply: A career at ESS gives you the opportunity to contribute to the future discoveries within neutron science at a stunning, brand-new workplace filled with innovative minds and brilliant people from across the globe. We offer market competitive, individualised compensation which is differentiated according to role, responsibilities, individual skills, abilities and achievements as well as monthly pension contributions on top of your salary. If you see yourself in what we’re looking for, please provide your CV and motivation letter in English by clicking on “apply” and following the instructions. Please be aware that we can only accept direct applications made via the ESS website, so submit your application as soon as you can. The last date for receiving applications is August 25th. Please note that 1st zoom interviews will take place mid September and onsite interviews mid October. For further information regarding the position, please contact Talent Acquisition Specialist Sofie Berg on sofie.berg@ess.eu or Hiring Manager Hanna Wacklin-Knecht - Head of the Scientific Support Division on mailto:hanna.wacklin-knecht@ess.eu For more information regarding the ESS recruitment process in general, please follow this link: https://europeanspallationsource.se/careersFor trade union information, please contact Unionen representative Nerusha Naicker on Nerusha.Naicker@ess.eu or SACO/Swedish Association of Graduate Engineers representative Marc Kickulies at Marc.Kickulies@ess.eu
Department of Molecular Sciences Third-cycle subject area: Chemistry Description of the doctoral project Do you want to work in a project that aims to replace fossil sources with forest raw materials for the production of biomaterials? Are you interested in immersing yourself in molecular interactions at the atomic level with advanced analytical instruments? Do you want to work with a whole group of researchers who share these interests? If so, this could be a PhD position for you. The overall goal of this PhD project is to enzymatically modify glycans from hemicellulose to produce bio-based crosslinkers for applications in adhesives, hydrogels and other crosslinked materials. However, many materials that we consider bio-based, such as wood fibreboards, hydrogels and stabilizers from non-fossil polymers, still rely on crosslinkers that have fossil origins and are often very harmful chemicals. Fibreboards for furniture, construction and insulation typically contain around 9% glue consisting of urea formaldehyde. Formaldehyde is classified as a known human carcinogen and its emissions from fibreboards are a major concern. Oxidative enzymes will be used on hemicellulose substrates, such as xyloglucan and glucomannan, to obtain aldehyde and ketone functions on the sugar ring in parallel with a partial degradation to oligosaccharides. The expected result is a collection of non-toxic, bio-based crosslinkers that can potentially replace formaldehyde and similar fossil-based crosslinkers. About the position You will be part of a research group conducting research in organic chemistry and biotechnology with a focus on structural analysis of enzymes and carbohydrate substrates using NMR spectroscopy, as well as the development of new methods for studying interactions between proteins and carbohydrates using NMR spectroscopy. The project includes a lot of laboratory work and will be carried out with an advanced level of characterization using NMR spectroscopy and mass spectrometry to be able to draw conclusions about the structural composition of the crosslinkers and the crosslinked materials. To achieve these goals while ensuring a productive and enriching environment, the project includes supervision in organic chemistry, enzymology and wood technology. The position also includes teaching up to 20% of the time. Requirements To meet the general entry requirements you must have: been awarded a second-cycle (Master’s) qualification; satisfied the requirements for courses comprising at least 240 credits of which at least 60 credits were awarded in the second-cycle, or acquired substantially equivalent knowledge in some other way in Sweden or abroad (Higher Education Ordinance 1993:100, Chapter 7, Section 39). Specific entry requirements for the third-cycle courses and study programme in chemistry: To meet the specific entry requirements, you must have at least 60 HEC in chemistry-related subjects (general, analytical, inorganic, organic and physical chemistry as well as biochemistry). This must include a degree project and at least 30 HEC must be at second-cycle level. You must also meet the equivalent English language requirements as those necessary for the Swedish upper-secondary qualification Engelska B/6. Your profile We are looking for a highly motivated candidate who has a master's degree in a field relevant to the position, for example in organic chemistry, biotechnology, molecular biology or equivalent. A focus on biochemistry or organic chemistry with experience in laboratory work are valuable merits, as are experience in NMR spectroscopy and/or protein expression and purification. Great emphasis is placed on personal qualities such as collaborative skills, analytical and problem-solving skills, as well as the ability to work independently. Good knowledge of English (both spoken and written) is required. About us You will be placed in the subject of organic chemistry at the Department of Molecular Sciences, SLU, Uppsala. The department consists of about 100 employees and, together with three other departments, forms an inspiring research environment at the BioCenter on the Ultuna campus in Uppsala. At the BioCenter there is broad expertise in plant biology, plant pathology, plant genetics, mycology, microbiology, food science, chemistry and biotechnology. We have access to advanced infrastructure such as a fermentation lab, advanced microscopy, X-ray diffraction, mass spectrometry and NMR spectroscopy. The department conducts research and teaching in chemistry, biotechnology, food science and microbiology. Our research projects include among other things enzymatic degradation of forest raw materials, production of fish feed from yeasts, programmed cell death in plants and biogas production. More information about the department is available at https://www.slu.se/en/about-slu/organisation/departments/molecular-sciences/. Read more about staff benefits and life as an SLU employee on https://www.slu.se/en/about-slu/work-at-slu/ Read more about third-cycle courses and study programmes onhttp://www.slu.se/utbildning/program-kurser/forskarutbildning/ Form of employment Employment as a doctoral student (4-year programme). Doctoral student’s salaries are set following the local collective agreement. Salary progression is fixed. Scope: 100% Location: Uppsala Start date: Upon agreement, but no later than December 2026. Application and selection: Please submit your application using the link below. The deadline is August 5, 2026. Read more about the attachments that your application should include at https://www.slu.se/en/study/programmes-courses/doctoral-education/how-can-i-become-a-doctoral-student/application/ Selection among eligible applicants is based on the documents attached to the application, and is carried out with regard to the applicant’s ability to complete the programme within the allotted time. Academic union representatives: https://internt.slu.se/en/my-employment/employee-associations/kontaktpersoner-vid-rekrytering/ Note: This is a shortened version of the advertisement adapted to the Swedish Public Employment Service’s (Platsbanken) system. Please see the full advertisement on SLU’s website: https://www.slu.se/en/about-slu/work-at-slu/jobs-and-vacancies/
We are looking for a Doctoral student to become part of our team at the Division of Nano and Biophysics at the Department of Physics and Astronomy. Join our innovative team and contribute to exciting research in developing materials for tomorrow's applications in medice and quantum technology in a collaborative, international and dynamic environment. We use state-of-the-art advanced instruments for understanding how to mechanisms determining the materials properties and enabling the design materials and devices. We collaborate with research groups in academia and industry to complete the chain from material fabrication, device development, structural and properties characterisation and application of the devices. About us Division of https://www.chalmers.se/en/departments/physics-and-astronomy/research/nano-and-biophysics/ is working at the forefront of experimental and theoretical research in the field of electron microscopy and correlation of atomic structure to properties. We combine world-class infrastructure, including the access to MC2 clean room and Chalmers materials analysis laboratory with state-of-the-art electron microscopes. The specific mission of Eva Olsson Group is to understand fundamental mechanisms that determine the properties of materials and enable the design of materials for tomorrow using advanced and state-of-the-art electron microscopy. We also develop new methods for correlating atomic structure to properties. We have a wide spread international collaboration network. From quarks to the cosmos – atoms to devices. At https://www.chalmers.se/en/departments/physics-and-astronomy/, we explore everything from the smallest scale to the largest, in order to understand, explain and improve our lives. About the research project The focus of the project is to develop new and more efficient X-ray detectors. One important aspect is that they are flexible which is well suited for applications in medicine and diagnostics. The research will be carried out within the framework of a collaboration project with Linköping University and Uppsala University. The project is entitled " Flexible X-ray detectors based on novel high-Z covalent organic frameworks" and is funded by the Knut and Alice Wallenberg Foundation. Who we are looking for The following requirements are mandatory: To qualify as a Doctoral student, you must have a Master's degree (masterexamen) of 120 credits or a Master’s degree (magisterexamen) of 60 credits* in physics. Strong written and verbal communication skills in English Course credits from one or more courses that include crystallography, diffraction and the theory of reciprocal space *for students with an education earned outside of Sweden, a 4-year Bachelor’s degree is accepted. The following experience will strengthen your application: Experience in using electron microscopes Experimental experience in high resolution imaging and diffraction using transmission electron microscopes Experimental experience of using energy dispersive x-ray spectroscopy in electron microscopes Experience in speciemn preparation for transmission electron microscopy What you will do Take courses at an advanced level within the Graduate school of https://www.chalmers.se/en/research/we-train-new-researchers/graduate-schools/physics/ Develop your own scientific concepts and communicate the results of your research verbally and in writing The position generally also includes teaching on Chalmers' undergraduate level or performing other duties corresponding to 20 percent of working hours Use and further develop techniques for advanced electron microscopy Contract terms The Doctoral student positions are fully funded from start. The position is a fixed-term appointment of four years, with the possibility to teach up to 20%, which extends the position up to five years. A starting salary of 35,725 SEK per month (valid from May 1, 2026). Doctoral studies require physical presence throughout the entire study period. A valid residence permit must be presented by the study start date; otherwise the admission may be withdrawn. What we offer As a Doctoral student at Chalmers, you are an employee and enjoy all employee benefits. Read more about https://www.chalmers.se/en/about-chalmers/work-with-us/ and our https://www.chalmers.se/en/about-chalmers/work-with-us/chalmers-as-an-employer/benefits-and-conditions/ for employees. A dynamic and inspiring working environment in the coastal city of https://www.goteborg.com/en. Read more about Sweden’s generous parental leave, subsidized day care, free schools, healthcare etc at https://www.movetogothenburg.com/ Chalmers is dedicated to improving gender balance and actively works with equality projects, such as https://www.chalmers.se/en/about-chalmers/organisation-and-governance/equality/genie-gender-initiative-for-excellence/. We celebrate diversity and consider equality and inclusion as fundamental aspects of all our activities. If Swedish is not your native language, Chalmers offers Swedish courses to help you settle in. Find more general information about doctoral studies at Chalmers https://www.chalmers.se/en/research/we-train-new-researchers/about-doctoral-studies/. Application procedure The application should be written in English and attached as PDF-files, as below. Maximum size for each file is 40 MB. Please note that the system does not support Zip files. CV Personal letter A brief introduction about yourself. A brief motivation as to why you are interested in this position. Bachelor’s and, if available, master’s thesis together with the transcripts. Use the button at the foot of the page to reach the application form. A background check may be conducted as part of the application process. Please note: The applicant is responsible for ensuring that the application is complete. Incomplete applications and applications sent by email will not be considered. Contact details to references will be requested after the interview. We welcome your application no later than July 31, 2026 For questions, please contact: Eva Olsson Professor mailto:eva.olsson@chalmers.se We look forward to your application! *** Chalmers declines to consider all offers of further announcement publishing or other types of support for the recruiting process in connection with this position. ***
Vill du skapa ny teknik i stället för att bara vänta på den? Hos Syntronic ligger vi steget före och är i teknikens framkant. Vi vill blir fler Integrationsingenjörer på Syntronic och söker dig som vill bli en del av vårt team bestående av experter i en internationell miljö. Arbetet innebär att du kommer att jobba med integration och verifiering av de senaste 5G radioprodukterna. Som Integrationsingenjör kommer du bland annat att arbeta med: Integration av mjukvara och hårdvara Felsökning och problemlösning Funktions- och verifieringstester Analysera krav och skriva testspecifikation Validera testutrustning. Som Integrationsingenjör på Syntronic kommer du främst jobba inom telekom. Ditt arbete har en internationell miljö och du får tillsammans med dina kollegor utvecklas inom avancerad RF-teknik. Dina uppdrag kommer i första hand att utföras in-house på Syntronic men kan också vara ute hos någon av våra kunder. Vi söker en Integrationsingenjör som: Har en högskole- eller civilingenjörsexamen eller annan relevant utbildning inom exempelvis Radio, Elektro, Teknisk fysik, eller motsvarande Är analytisk och noggrann Kommunicerar flytande på svenska och engelska i både tal och skrift. Det är meriterande om du som Integrationsingenjör har: Tidigare arbetat med Elektronikkonstruktion, gärna mot RF Mjukvaruerfarenhet (Linux, HP Vee, m.m.) Erfarenhet av arbete i labbmiljö med avancerade mätinstrument så som signalgenerator och spektrumanalysator Erfarenhet av att analysera testdata. Syntronic erbjuder en trygg anställning i en dynamisk och framåtriktad miljö. Att vi är ett team är vår styrka, därför ser vi att du arbetar tillsammans på plats med oss på kontoret – när du inte behövs hos någon av våra kunder förstås! På vårt huvudkontor i Gävle har vi labb på över 1500kvm med den senaste avancerade utrustningen för att kunna arbeta med digital och analog utveckling. Personliga egenskaper Vi ser att du som Integrationsingenjör hos oss är driven, flexibel och självgående med en stark teamkänsla. Det är viktigt att du är kreativ och arbetar med ett engagemang och driv för dina arbetsuppgifter. Du har en god social kompetens men kan även vid behov arbeta självständigt och vet när det är dags att fokusera. Vi ser också gärna att du är analytisk, logisk, metodisk och strukturerad samt kan hantera flera uppgifter parallellt. Vi erbjuder På Syntronic blir du en del av en härlig gemenskap där din röst hörs och dina idéer välkomnas. Vi erbjuder flexibla arbetstider, balans mellan arbete och fritid samt regelbundna karriärutvecklingssamtal och interna workshops för din utveckling. Utöver detta får du riktigt bra förmåner och försäkringar. Hos oss får du inte bara ett jobb - du får en plats att växa och trivas både personligt och professionellt. Välkommen till Syntronic! Ansökan Ansök senast 5/8. Under sommar och semestertider kan återkoppling på din ansökan och rekryteringsprocessen för tjänsten ta längre tid än vanligt. Vi uppskattar ditt tålamod och ser fram emot att ta del av din ansökan. Av kommunikation- och kvalitetssäkringsskäl ber vi dig att skicka in din ansökan digitalt via vårt system och inte via e-post. Vi kan använda AI och automatiserade verktyg som stöd i vår rekryteringsprocess. Alla beslut om urval och anställning fattas alltid av människor.
The opportunity Innovation is the heart of Hitachi Energy, and our research centres are its backbone. Join us if you have scientific or technical expertise as well as drive and passion for research. You will work in a dynamic, motivated, and creative team with a wide range of experience and competence and with access to advanced laboratory facilities. We are looking for a research scientist with expertise experimental applied physics to join the Applied Physics team at our research center in Västerås, Sweden. You will lead multidisciplinary research projects developing cutting-edge technologies for future Hitachi Energy products. How you'll make an impact Together with your colleagues, solve challenging R&D problems using a combination of analytical, computational and experimental methods. With support from operation specialists, test and validate your ideas by building prototypes, and experiments in the labs or on pilot units. Build your network in the company and actively disseminate your results in presentations, technical reports, patent applications, and scientific publications. Work closely with our global multidisciplinary team of researchers and operation specialists in Hitachi Energy Research, our business units, universities and industrial partners. Propose and lead technology development projects to bring innovative new ideas from concepts to solutions ready for handover to the R&D product development teams. Learn about Hitachi Energy products. Identify issues, possible improvements and challenge established designs. Keep up with the latest development from competitors and academia, to contribute to shaping Hitachi Energy’s technology strategy. Continuously learn new methodologies and tools within your competence area and apply them to Hitachi Energy’s products and applications. Your background Required: PhD in physics, preferably with a focus in high-voltage or dielectrics. Excellent leadership and communication skills, team player attitude, initiative, and creativity. Fluent in English, both written and spoken. Considered a strong advantage: Experience with high voltage insulation systems. Hands‑on experience measuring high‑field phenomena, including partial discharge, electrical breakdown, electromagnetic fields, and shockwaves in gaseous or liquid environments. Hands-on experience using instruments such as voltage and current probes, photodiodes, silicon photomultipliers, scientific cameras (high speed or high sensitivity), oscilloscope, lock in amplifiers, custom optical setups (e.g. shadowgraphy, polarimetry). Experience with numerical or multiphysics simulation tools, such as COMSOL, CST, ANSYS, or comparable open‑source packages. Experience with data analysis using scripting languages such as Python or Matlab. Nice to have: Experience designing and procuring simple mechanical parts or electronics using CAD / EDA engineering tools. Experience or interest developing machine learning application. More about us What We Offer: • Collective agreement • Flexible working time • Health care and wellness allowance • Fantastic career possibilities within Hitachi Energy both within Sweden and globally • A mentor to support you throughout the onboarding phase • Various trainings and education supporting employee development • Diversified company with over 70+ nationalities working in Sweden • Supplementary compensation for parental leave • Employee Benefit Portal with thousands of discounts and perks Are you ready for a new exciting challenge? Does the above description sound like you? Applications will be reviewed on an ongoing basis, so don’t delay – apply today! Recruiting Manager Swann Levasseur, swann.levasseur@hitachienergy.com will answer your questions about the position. Union representatives - Sveriges Ingenjörer: Bo Westman, +46 107-38 38 04; Unionen: Karin Ulvemark, +46 107-38 51 42; Ledarna: Frank Hollstedt, +46 107-38 70 43.
The opportunity Innovation is the heart of Hitachi Energy, and our research centres are its backbone. Join us if you have scientific or technical expertise as well as drive and passion for research. You will work in a dynamic, motivated, and creative team with a wide range of experience and competence and with access to advanced laboratory facilities. We are looking for a research scientist with expertise experimental applied physics to join the Applied Physics team at our research center in Västerås, Sweden. You will lead multidisciplinary research projects developing cutting-edge technologies for future Hitachi Energy products. How you'll make an impact Together with your colleagues, solve challenging R&D problems using a combination of analytical, computational and experimental methods. With support from operation specialists, test and validate your ideas by building prototypes, and experiments in the labs or on pilot units. Build your network in the company and actively disseminate your results in presentations, technical reports, patent applications, and scientific publications. Work closely with our global multidisciplinary team of researchers and operation specialists in Hitachi Energy Research, our business units, universities and industrial partners. Propose and lead technology development projects to bring innovative new ideas from concepts to solutions ready for handover to the R&D product development teams. Learn about Hitachi Energy products. Identify issues, possible improvements and challenge established designs. Keep up with the latest development from competitors and academia, to contribute to shaping Hitachi Energy’s technology strategy. Continuously learn new methodologies and tools within your competence area and apply them to Hitachi Energy’s products and applications. Your background Required: PhD in physics, preferably with a focus in high-voltage or dielectrics. Excellent leadership and communication skills, team player attitude, initiative, and creativity. Fluent in English, both written and spoken. Considered a strong advantage: Experience with high voltage insulation systems. Hands‑on experience measuring high‑field phenomena, including partial discharge, electrical breakdown, electromagnetic fields, and shockwaves in gaseous or liquid environments. Hands-on experience using instruments such as voltage and current probes, photodiodes, silicon photomultipliers, scientific cameras (high speed or high sensitivity), oscilloscope, lock in amplifiers, custom optical setups (e.g. shadowgraphy, polarimetry). Experience with numerical or multiphysics simulation tools, such as COMSOL, CST, ANSYS, or comparable open‑source packages. Experience with data analysis using scripting languages such as Python or Matlab. Nice to have: Experience designing and procuring simple mechanical parts or electronics using CAD / EDA engineering tools. Experience or interest developing machine learning application. More about us What We Offer: • Collective agreement • Flexible working time • Health care and wellness allowance • Fantastic career possibilities within Hitachi Energy both within Sweden and globally • A mentor to support you throughout the onboarding phase • Various trainings and education supporting employee development • Diversified company with over 70+ nationalities working in Sweden • Supplementary compensation for parental leave • Employee Benefit Portal with thousands of discounts and perks Are you ready for a new exciting challenge? Does the above description sound like you? Applications will be reviewed on an ongoing basis, so don’t delay – apply today! Recruiting Manager Swann Levasseur, swann.levasseur@hitachienergy.com will answer your questions about the position. Union representatives - Sveriges Ingenjörer: Bo Westman, +46 107-38 38 04; Unionen: Karin Ulvemark, +46 107-38 51 42; Ledarna: Frank Hollstedt, +46 107-38 70 43.
Lyten Labs is seeking a talented Analytical Chemist. As Analytical Chemist you are responsible for the development, validation, and implementation of analytical methods for analysing incoming material, intermediate and finalized products for Research & Development, Production, and external suppliers on a wide range of instruments. Strict adherence to the principles of Quality Assurance, Quality Control, and Quality Management System requirements (ISO 9001, IATF 16949, ISO- IEC 17025, etc.). Proven track record in statistical analysis and measurement system analysis (MSA). Participating in problem solving, technical troubleshooting exercises, and technical discussions where needed. Mentoring and training for technicians. Key responsibilities (not limited to) Develop, validate and document analytical methods and procedures for analyzing and characterizing new incoming and raw materials and product intermediates. Optimize analytical methods to increase efficiency and turn-around time of the laboratory. Execute the Quality Control and testing plan of raw materials and product intermediates. Troubleshoot and maintain the analytical instruments to a high standard. Understand and internalize QA/QC principles in everyday functions. Work across many parts of the organization, collaborating with production teams, Process engineering in R&D and production, Supply Chain, IT & automation. Start-up of first analytical methods and instruments. Specific expertise in ICP-OES/MS, ED-XRF, XRD, SEM-EDX, Titration, TGA/DSC, etc. Qualifications/education/experience MSc or PhD degree in Chemistry, preferably, Analytical Chemistry. 5+ years of relevant work experience in a laboratory environment. Specific knowledge of quality management systems, e.g. ISO 9001, IATF 16949, and ISO- IEC 17025. Experience in developing and validating analytical methods, standards, procedures and documentation in an efficient way. Project management skills and a successful track record of leading quality projects in a laboratory environment. Knowledgeable in Lean and six sigma. Familiar with SPC, FMEA, Quality troubleshooting tools and problem-solving methodology. Curious, technically educated and preferably with a strong business background.
Job Scope High level purpose of function. Responsible for the development, validation, and execution of the methods used for material analysis, including incoming material, intermediate, and finalized products for Research & Development and Production on a wide range of instruments. Strict adherence to the principles of Quality Assurance in Quality Control (QA/QC). Proven track record in statistical analysis and measurement system analysis (MSA). Key Responsibilities Overall areas of responsibilities and activities. Key responsibilities include (but are not limited to) Responsible for a set of instrumentation or measurement systems. This involves, but not limited to, coordinating maintenance and troubleshooting, writing support documentation, training and qualifying personnel, performing method development and validation. Understand and internalize QA/QC principles in everyday functions. Conduct analysis on a wide range of instruments and report data/results for a diverse set of samples. Execute the Quality Control and testing plan of material and components. Maintaining instruments and measurement areas to a high standard, involving ownership of room(s)/area(s) to drive safety related topics, ensure 5S, maintain consumable inventory and standards/reference samples. Work across many parts of the organization, collaborating with R&D technical team, Process Quality Engineering, Process Engineering, Supply Chain, IT & automation. Drive operational excellence and investigations by being a key player in problem solving and process improvement exercises. Accountability/Authorization Budget responsibility: No Direct reports: No Work Environment responsibility: No All employees are accountable for complying with safety regulations and actively supporting a safe workplace. Requirements Educational background and previous experience required for the role. Qualifications and experience Minimum MSc degree or Bachelor’s degree with 5+ years of work experience in a laboratory, in Chemistry, Material or Mechanical Engineering. 3+ years of relevant work experience in relevant laboratory environment. Experience of laboratory work in relevant industries such as, e.g. Li-ion materials, Pharmaceutical, Food and Paper industries or automotive industries. Experience in developing methods, standards, procedures, and documentation in an efficient way. Familiarity with Statistical Process Control (SPC), Failure Mode and Effects Analysis (FMEA), Control Plan (CP), Lean, Six Sigma , Quality troubleshooting tools and problem-solving methodology. Specific skills & Knowledge Specific knowledge in any relevant instrumentation, measurement system, or scientific field used by the company. Knowledgeable in Laboratory Information Management System (LIMS), quality management systems, e.g. ISO 9001, IATF16949, Total Quality Management (TQM). Project management skills and a successful track record of leading quality projects in a laboratory environment. Excellent English skills, both written and oral, are essential. Basic Swedish and other language skills are a plus. You should have good communication skills and be able to work in close collaboration with colleagues from many different teams.
Do you have deep expertise in fluidics and flow-cell design for analytical instrumentation? Are you excited by the opportunity to drive development from early concepts to production and product care? Join Moleculent and play a key role in developing a cutting-edge life science instrumentation! Moleculent is on a mission to build products that yield new insights into the molecular foundation of human biology. This is a chance to join a focused and dedicated team with extensive experience building successful life-science companies and products. This is a permanent position based in Solna, Stockholm. The position is full-time and based at Moleculent’s headquarters in Solna, Stockholm. Please don’t wait to submit your application. We review candidates on an ongoing basis, and the position may be filled before the final application deadline. Applicants must be eligible to work in Sweden without sponsorship. JOB DESCRIPTION As a Senior Systems Engineer – Fluidics at Moleculent, you will be responsible for flow cells and fluidics design throughout the entire product development life cycle – from concept development and prototyping to design transfer and product care. You will work closely with cross-functional teams and external partners to develop robust and scalable solutions for advanced analytical instrumentation. You will combine hands-on laboratory work with system-level thinking and project leadership responsibilities. Key responsibilities include: Lead flow cell and fluidics design activities, including design, testing, troubleshooting, and verification Drive development of new flow cell concepts and consumable designs Support flow cell production engineering and production troubleshooting Ensure production equipment is maintained, supported, and qualified Participate in and drive instrument-level testing and verification activities Lead or contribute to throughput improvement initiatives Manage system-related project activities and integration work Contribute to early-stage conceptual development for future instrument generations Collaborate closely with R&D, Operations, Product Management, Biochemistry teams, suppliers, and contract manufacturers QUALIFICATIONS To fit the role, you most likely hold an MSc in Technical Biology, Molecular Biotechnology, Material Science, Mechanical Engineering, or a related field. A PhD within a relevant discipline is considered a strong advantage. Fluent written and spoken English is required. You have several years of experience working with fluidics and flow cell development in analytical or life science instrumentation environments. You are comfortable moving between development, testing, production support, and cross-functional collaboration. We believe you have: Experience with fluidics design in analytical systems Experience with consumable prototyping, product development, and transfer to manufacturing Knowledge of plastics and adhesives commonly used in life science or medical technology products Experience from product development of instrumentation within Life Science Hands-on laboratory experience and practical troubleshooting skills Project management or project leadership experience Experience with testing, verification, and troubleshooting activities Good understanding of integrated hardware/software instrumentation systems Nice to have: Experience with flow simulations Experience with requirements engineering and formal verification methodologies Experience working with analytical instruments, in vitro diagnostics systems, or medical devices Experience writing test specifications and verification documentation Swedish language skills You are hands-on, analytical, and solution-oriented, with a strong ability to navigate complex technical challenges. You enjoy working closely with both development and production teams and thrive in collaborative environments where innovation and quality are central. You are structured in your approach while remaining pragmatic and adaptable in a fast-moving environment. You take ownership of your work and enjoy driving projects forward together with others. MOLECULENT We believe innovative biotechnology has enabled massive leaps forward in understanding the composition of tissues and organs. However, the functional understanding of how cells communicate in their native context and form these complex systems has just begun. We develop technology designed to uncover radical new insights into the cellular level of human biology by mapping the communication between cells in human tissue and providing meaningful data. https://www.moleculent.com/ Please note that Moleculent manages the recruitment process for this position. External recruitment agencies are requested to refrain from direct contact with us in this regard.
Gnothis AB is seeking for a hands-on engineer who enjoys building experimental systems in a laboratory environment. The role combines microfluidics integration, instrument prototyping, and Python-based automation. This is a permanent position based at our HQ, located at the campus of Stockholm University (Stockholm, Sweden). Gnothis, founded in 2015 and supported by highly innovative industrial professionals and technology developers, is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for the diagnosis of complex diseases. Gnothis technology integrates a wide range of cutting-edge sciences ranging from nanotechnology, photophysics, optics, surface chemistry, biochemistry and computational science. Since we have taken significant steps forward and now need to solve the remaining crucial challenges before commercialization; for the right person this is a unique opportunity to become a valuable member, to use your “think-outside-the box” mentality with aim to develop a new world-class technology platform! Our instrumentation, software and analysis team currently consists of four engineers and we are now expanding the team as we scale development of the system. The work is primarily on-site and very practical, involving both hardware integration and control software development. The position is part of a multidisciplinary team developing a prototype DNA sequencing instrument combining microscopy, microfluidics, nanofabrication and advanced data analysis. Initial Project The first major task will be to design and integrate a microfluidics subsystem into our existing microscope prototype – to plan, test, order and add already commercially available components to a final prototype. This includes selecting and integrating a commercial microfluidics system (e.g. Elveflow or similar), designing a custom sample chip holder and fluid interface, integrating control into an existing Python control software, and establishing practical operation and cleaning procedures. The work is supported by a biochemistry team, but we are seeking for the right candidate who can make confident engineering decisions based on previous hands-on experiences connected to eg. microfluidics and laboratory automation. Responsibilities Mechanically integrate new devices into a prototype life-science instrument. The initial focus is on liquid sample handling, such as flow and temperature control. Develop Python control and automation software, starting from existing vendor SDKs. Design simple mechanical parts (CAD / 3D printing) Hands-on prototyping and debugging in the lab Method development for instrument performance evaluation and self-calibration. Over time the role will involve increasing focus on automation and device control software. Candidate Profile For you to enjoy performing expected activities, and being a valuable member in an ambitious and innovative team; we think you are an engineer with a strong creative mindset and with strong previous experience building/developing scientific or laboratory instrumentation. This role suits someone who enjoys experimental prototyping in a small startup environment. The candidate should be comfortable collaborating in a multidisciplinary research environment consisting of engineering, software, biochemistry and nanofabrication experts. Relevant backgrounds and skills include: Master of Science and/or Ph.D. educational background – ideally combined with a relevant Life Science focus. Practical experience with microfluidics systems Python programming for hardware control Comfortable with hands-on lab engineering (CAD, electronics, prototyping) Microscopy / Optics / Imaging Lab automation / Liquid handling Mechatronics / Robotics A recent Ph.D. with strong hands-on instrument development experience could also be a good fit for this position. Gnothis offer a creative environment focused on technology and product development, a competitive compensation package and plenty of room for self-development as the company expands. This is a permanent position (not consultant assignment). If above sounds like an exciting opportunity and you would like to hear more, do not hesitate and submit your application and we will get back to you! Gnothis AB on LinkedIn: https://www.linkedin.com/company/gnothis/posts/?feedView=all For inquires please email us at: markus.dahl@valleyrecruitment.se
APL, Apotek Produktion & Laboratorier AB, har till uppgift att tillverka extemporeläkemedel som är ett individanpassat läkemedel för en enskild patient, i syfte att förbättra och rädda liv. Många beredningar görs till barn och till vuxna med olika typer av överkänslighet. APL är statligt ägt och en av Europas största tillverkare av extemporeläkemedel och är även en etablerad kontraktstillverkare inom Life science-industrin med resurser för utveckling, tillverkning och analys av läkemedel. APL:s ca 600 medarbetare är verksamma vid fem tillverkningsenheter runt om i Sverige. Läs gärna mer på www.apl.se Nu söker vi en Mikrobiolog som är nyfiken på och har intresse av att utvecklas inom vårt breda och varierade sortiment av läkemedel som gör skillnad för patienter med särskilda behov. Tjänsten Du kommer att ingå i ett sammansvetsat team som karaktäriseras av ett öppet klimat med tydligt samarbetsfokus där alla hjälps åt för att säkra att vi håller hög kvalitet genom alla processer både utifrån korta och långsiktiga deadlines. Analys av läkemedel, råvaror och vatten utförs enligt metoder beskrivna i den europeiska farmakopén såsom bestämning av halt levande mikroorganismer och tester för specifika, sjukdomsalstrande mikroorganismer. Tillverkningslokaler kontrolleras genom partikelmätning samt analys av antal levande mikroorganismer i luft och på ytor. Vid behov utförs identifiering av mikrobiologiska isolat. Beredning av odlingsmedier och andra reagens kan också ingå i arbetsuppgifterna, likaså validering av metoder, instrument och lokaler. Arbetet utförs enligt GMP med allt vad det innebär i form av dokumentation, avvikelsehantering, ändringshantering mm. Mikrobiologisk analys av prover från andra läkemedelsföretag ingår i verksamheten och samverkan med externa kunder är en del av dina dagliga uppgifter. Huvudsakliga arbetsuppgifter Laborativt arbete i form av mikrobiologiska analyser. Genomföra avvikelseutredningar och förbättringarbete Instrumentansvar Tjänsten är en tillsvidareanställning som kan komma att inledas med en provanställning. Arbetstiden är heltid 40 timmar i veckan och är förlagd på dagtid måndag till fredag. Tillsättning sker enligt överenskommelse och placeringsort är Malmö. Vem är du Vi söker dig som har akademisk utbildning med inriktning på mikrobiologi eller motsvarande erfarenhet. Du har 2-5 års erfarenhet av arbete på ett mikrobiologiskt laboratorium. Vi ser gärna att du har erfarenhet av mikrobiologisk kontroll av vatten, råvaror, förpackningar, men även av hygienprovtagning Erfarenhet av rapportskrivning Goda kunskaper om GMP och tillhörande regelverk Erfarenhet av lean, förbättringsarbete samt molekylärbiologisk arbete är meriterande Goda kunskaper i svenska och engelska i såväl tal som skrift Vi söker dig som är erfaren, kunnig och trivs med laborativt arbete. Viktiga personliga egenskaper är att du kan arbeta både självständigt och tillsammans i ett team. Du kan snabbt sätta dig in i nya komplexa frågeställningar och har en god analytisk förmåga. APL kännetecknas av en öppen och dynamisk atmosfär med korta beslutsvägar. För att du ska trivas behöver våra värderingar affärsmässig, lyhörd, lösningsorienterad och ansvarstagande passa in på dig. Alla medarbetare har en individuell utvecklingsplan och tydliga mål som kontinuerligt följs upp. Detta ger var och en möjligheten att påverka sin egen situation och bidra till vår gemensamma utveckling och vi uppmuntrar aktivt till intern rörlighet. Du får tillgång till en förmånsportal där vi samlar våra förmåner och erbjudanden, t ex friskvårdsbidrag och kostförmån. Vi har kollektivavtal med Unionen och SACO och därtill hörande förmåner, exempelvis tjänstepension, försäkringar, flextid och lediga klämdagar. På samtliga orter finns friskvårdsgrupper som arrangerar olika typer av aktiviteter. Ansökan Sista ansökningsdag är 2026-07-28. Ansökan görs via länken i annonsen, vi tar inte emot ansökningar via e-mail. För information Vid frågor om tjänsten är du varmt välkommen att kontakta Ingela Engbe via e-post: ingela.engbe@apl.se eller telefon:+708 210666. Övrigt Innan ev. anställning kommer du att få göra ett alkohol-/drogtest samt att vi utför en bakgrundskontroll på dig via Bakgrundskollen.se. Välkommen att dela en spännande framtid med oss på APL!
The Opportunity We are looking for a Regional IT/OT Specialist to support the delivery, operation, and continuous improvement of IT/OT services across factory sites, workshops, and laboratories in Europe within Hitachi Energy’s Service Business. In this role, you will combine hands-on technical expertise with collaboration across teams to ensure reliable and secure operations. You will play a key role in supporting critical systems, enhancing cybersecurity, and acting as a bridge between business stakeholders, vendors, and Group IT. This position offers a dynamic industrial environment with exposure to operational technology, laboratory systems, and continuous improvement initiatives. How you'll make an impact Provide on-site and remote IT/OT support for hardware, software, and connectivity across factories, workshops, and laboratories Perform hands-on support at regional sites and travel as required to ensure operational continuity Maintain and support locally managed systems and equipment outside Global IT coverage Manage and support IT/OT applications, including coordination with external vendors Support laboratory instruments, ensuring reliable connectivity, data transfer, and integration with business systems Maintain operational technologies such as collaboration tools, security systems, and badging solutions Implement and support cybersecurity measures, including system configuration, patching, and incident response Ensure services are delivered in compliance with company standards, policies, and regulatory requirements Collaborate with stakeholders and vendors while documenting solutions and driving continuous improvement Willing to travel ca 40 % of your work time and you always represent Hitachi Energy the best possible way Your Background 3–5+ years of hands-on experience in IT/OT support, service delivery, or infrastructure within industrial, manufacturing, or laboratory environments Experience with manufacturing processes, OT environments (e.g., MES), or LIMS is considered an advantage Experience supporting end-user hardware, software, networking, and connectivity Experience working with vendors and supporting operational technology systems Solid understanding of cybersecurity fundamentals, patching, and secure system configuration Strong problem-solving skills with a proactive and solution-oriented mindset Ability to work independently and collaborate effectively across teams Proficiency in English and knowledge of one or more Nordic languages is a must ITIL4 certification is a plus What we offer (relevant for Sweden) Collective agreement Flexible working time Health care and wellness allowance Fantastic career possibilities within Hitachi Energy both within Sweden and globally Mentor to support you throughout onboard phase Various trainings and education supporting employee development Diversified company with over 70+ nationalities working in Sweden Supplementary compensation for parental leave Employee Benefit Portal with thousands of discounts and perks More about us The position is based in Ludvika, Drammen or Vaasa. Are you ready for a new exciting challenge? Does the above description sound like you? Applications will be reviewed on an ongoing basis, so don’t delay – apply today! Union representatives – Sveriges Ingenjörer: Anna Sävenstedt, +46 73 0669908; Unionen: Tomas L. Gustafsson, +46 10 7382747; Ledarna: Frank Hollstedt +46 10 7387043. Any other questions can be directed to Talent Partner Antra Volujevica antra.volujevica@hitachienergy.com.
Do you thrive on bringing structure to complexity? Are you excited by the opportunity to shape how requirements, architecture, and change flow through a growing engineering organization? Join Moleculent and play a key role in building the backbone of a cutting-edge life science instrumentation platform! Moleculent is on a mission to build products that yield new insights into the molecular foundation of human biology. This is a chance to join a focused and dedicated team with extensive experience building successful life-science companies and products. This is a permanent position based in Solna, Stockholm. We will review the applications after the vacation period. Applicants must be eligible to work in Sweden without sponsorship. JOB DESCRIPTION Working as a Senior System Engineer within R&D Instrument at Moleculent, you will support the development of innovative products for research applications in a fast-growing R&D environment. You will focus on requirements management, system design coordination, change management, and configuration management, while also helping establish and improve scalable engineering processes as the organization grows. You will combine structured systems thinking with hands-on cross-functional collaboration across biochemistry, software, mechanical, and electrical engineering. Key responsibilities include: Define, structure, and maintain system and stakeholder requirements with clear traceability through design and verification Coordinate system-level architecture and design activities across biochemistry, software, mechanical, and electrical engineering teams Facilitate technical reviews to ensure alignment between requirements and implementation Establish and continuously improve requirements, change, and configuration management processes Manage engineering changes, conduct impact assessments, and maintain controlled product baselines Support system integration, verification, and product release activities QUALIFICATIONS To fit the role, you most likely hold a degree in Systems Engineering, Mechanical Engineering, Electrical Engineering, Biomedical Engineering, or a related field. You have experience in systems engineering within the development of life science instruments, laboratory equipment, analytical instruments, or similar technology-driven products. Fluent written and spoken English is required. We believe you have: Strong understanding of requirements management and configuration/change control principles Experience introducing or scaling engineering processes in a growing organization A structured, hands-on mindset with strong cross-functional communication skills Experience supporting system integration, verification, and product release activities Experience in project management/ working as a team lead is considered very meriting The right candidate for the role combines strong technical leadership with an operative, hands-on approach. As a person, you are analytical, structured, detail-oriented, and dedicated to product quality. You are positive, communicative, and collaborative, and you enjoy working in a goal-oriented environment. You are driven by teamwork and have a pragmatic approach. You are friendly, positive, and fun to work with, and you enjoy working in a fast-paced, changing environment. MOLECULENT We believe innovative biotechnology has enabled massive leaps forward in understanding the composition of tissues and organs. However, the functional understanding of how cells communicate in their native context and form these complex systems has just begun. We develop technology designed to uncover radical new insights into the cellular level of human biology by mapping the communication between cells in human tissue and providing meaningful data. https://www.moleculent.com/ Please note that Moleculent manages the recruitment process for this position. External recruitment agencies are requested to refrain from direct contact with us in this regard.
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