Sökresultat för "biotechnology"

About the role At Navinci, we are passionate about understanding biology and disease at a deeper level. We develop technologies and applications that help researchers study proteins, signaling pathways, cellular biology, and molecular mechanisms directly in biological samples. Our work spans tissue and cell-based systems and increasingly combines information from multiple technologies and data types to generate richer biological insight. We collaborate with leading academic groups, biotech companies, and pharmaceutical partners worldwide to advance research and translational science. As we continue to grow, we are looking for 2–3 scientists with different backgrounds and expertise to join our R&D team. We are interested in people who are excited by science, enjoy solving complex problems, and want to contribute to the development of innovative research tools and technologies. Whether your background is in cell biology, tissue biology, spatial biology, immunology, biomarker research, assay development, translational science, omics technologies, or technology development, we would love to hear from you. What you will do Design, execute, optimize, and troubleshoot biological assays and laboratory experiments Analyze and interpret data, generate robust and reproducible results, and communicate clear conclusions Document experimental work according to quality standards and contribute to scientific decision-making Collaborate across R&D, Operations, and Commercial teams Support development of new applications, products, technologies, and improved ways of working Must-have qualifications MSc or PhD in Biotechnology, Molecular Biology, Cell Biology, Biochemistry, Immunology, Medical Science, or a related field Hands-on experience with immunofluorescence, immunohistochemistry (IHC), and other in situ staining and detection methods Experience working with both tissue samples and cell-based models Experience designing, executing, and troubleshooting biological experiments Strong skills in data analysis and presentation, experimental planning, and scientific documentation Fluent in English, written and spoken Experience in one or more of the following areas Cell culture and primary cell models RNA-based methods, transcriptomics, or other omics technologies Flow cytometry Multiplex imaging, microscopy, image analysis, or digital pathology Protein biomarker analysis and antibody-based assays Assay, application, or product development Translational research, biomarker discovery, or disease biology (e.g., oncology, immunology, neuroscience) Statistical analysis, automation, quality systems Industrial R&D, scientific publications, grant writing or patent-related activities Who you are Curious, innovative, and eager to solve scientific challenges Agile and adaptable, with the ability to work in a fast-moving environment Structured, organized, and committed to high scientific quality Hands-on, proactive, and solution-oriented Collaborative, supportive, and comfortable taking ownership of your work

Faculty of Natural Resources and Agricultural Sciences Department of Molecular Sciences Swedish University of Agricultural Sciences is a world-class university in the bio- and environmental sciences, with a vision to play a key role in advancing sustainable living through science and education. SLU offers an attractive research environment distinguished by its uniquely broad and internationally leading research, with excellent opportunities for multidisciplinary and interdisciplinary collaboration with research groups in the social sciences, economics, engineering, and other natural sciences. The Department of Molecular Sciences at SLU Uppsala is seeking an Associate Professor (University Senior Lecturer) in Food Biotechnology. The department currently comprises approximately 90 staff members and, together with three other departments, forms an inspiring research environment at BioCentrum. It encompasses several interacting disciplines, including food science, biotechnology, microbiology, inorganic, physical and organic chemistry, biochemistry, molecular structural biology, and natural products chemistry. Research at the department focuses on both applied and fundamental biological and chemical processes. Note: This advertisement is abbreviated to fit in Platsbanken's recruitment tool. To view the ad in its entirety including additional information, please visit Jobs and vacancies at SLU | Externwebben. More information about the department’s activities and infrastructure is available https://www.slu.se/en/about-slu/organisation/departments/molecular-sciences/. More information about our benefits and what it is like to work at SLU is available https://www.slu.se/en/about-slu/work-at-slu/.   Subject area The subject area encompasses food biotechnology, with a focus on the conversion of raw materials into food products primarily through the metabolic activity of microorganisms.   Duties The candidate should within the subject area develop and lead internationally successful research develop, lead and participate in teaching at first, second and third cycle level primarily teach in the areas of food science, microbiology, and biotechnology, as well as contribute to other teaching activities at first, second and third cycle level supervise doctoral students and contribute to the development of the postgraduate subjects biology and food science collaborate with other SLU research teams in order to strengthen interdisciplinary activities at the university develop and maintain national and international networks with academia, relevant public authorities, industry, organisations and society at large apply for external research funding contribute to the strategic development of the department, faculty and SLU communicate research findings and other relevant information to society at large perform administrative duties within the department, faculty and university. The department operates in a parallel-language working environment. The Senior Lecturer will be able to perform most of their duties in English. However, as a public authority, the university is required under the Language Act to use Swedish as its principal language, and the appointee is therefore expected to acquire sufficient proficiency in Swedish to communicate effectively within four years of taking up the position. The department will provide support to enable the appointee to achieve this.   Eligibility The applicant must meet the following qualification requirements: research expertise in the subject area teaching expertise and ability to integrate research and a scientific approach into teaching excellent proficiency in English. Grounds of assessment and other information Note: This advertisement is abbreviated to fit in Platsbanken's recruitment tool. To view the ad in its entirety including additional information, please visit Jobs and vacancies at SLU | Externwebben.   Application deadline: 2026-08-03 Place of work: Uppsala Extent: 100% Form of employment: Permanent employment Starting date: By agreement. Application:  For the guidance of your application, there is SLU's appointment procedure for teachers at SLU and General assessment criteria for the appointment of teachers, which you can https://internt.slu.se/stod-service/admin-stod/hr-fragor/rekrytering-till_alla_ovriga_anstallningar/anstallning-av-larare/. Please apply by clicking the apply-button below. Academic union representatives: https://internt.slu.se/min-anstallning/facket/kontaktpersoner/

Fakulteten för skogsvetenskap Wallenberg Initiatives in Forest Research (WIFORCE) är Sveriges största forskningsprogram inom skogsskötsel och skoglig genetik med en budget under perioden 2019-2030 med ca 900 mnkr inklusive medfinansiering. WIFORCE består av ett forskningsprogram inom Future Silviculture samt ett forskningsprogram inom Forest Biology and Biotechnology. WIFORCE inrymmer också en forskarskola med 51 doktorander och en WIFORCE Arena och ett datasupportcenter. Om jobbet Som koordinator kommer du att assistera programchefen för WIFORCE att koordinera forskningsprogrammet. Du kommer att vara kontaktperson inom WIFORCE för företag, industri och olika myndigheter som är medverkande inom forskningsprogrammet. Inom en del av anställningen som koordinator så kommer du att bevaka EU-frågor för fakultetens uppdrag.   Din bakgrund Vi söker dig som har forskarutbildning och du bör ha erfarenhet av att utbilda doktorander, gärna både nationellt och internationellt. Du bör också ha erfarenhet av att koordinera samarbetsprojekt mellan universitet och industri eller myndigheter. Som koordinator gillar du att samverka inom och utom fakulteten samt att engagera kollegor i verksamheten för att vi ska kunna genomföra ett framgångsrikt forskningsprogram. Erfarenhet av projektledning och nätverksbyggande är meriterande. Förmåga att uttrycka dig i tal och skift på svenska och engelska är ett krav. Eftersom arbetet är förenat med många kontakter både inom och utanför SLU fäster vi stor vikt vid dina personliga egenskaper vad gäller kommunikations-, samarbets-, initiativ- och organisationsförmåga. Vi ser gärna att du arbetar på plats för att främja samarbete och vår arbetsmiljö positivt, samtidigt finns det möjlighet att arbeta hemifrån när verksamheten tillåter. Om oss Fakulteten för skogsvetenskap (S-fakulteten) bedriver utbildning, forskning, miljöanalys och samverkan inom skogsvetenskap. Fakulteten har 11 institutioner med ca 700 anställda och en omsättning på 1,1 miljarder kr. Vid fakultetskansliet arbetar vi med övergripande planering, ekonomistyrning, utredningar och uppföljning inom fakultetens olika verksamhetsområden och vi svarar för administrativt stöd till fakultetsledningen samt fakultetsnämnden och dess nämnder och utskott. Mer information om institutionen/avdelningen: https://www.slu.se/om-slu/organisation/fakulteter/fakulteten-for-skogsvetenskap/ Läs mer om våra förmåner och hur det är att jobba vid SLU på https://www.slu.se/om-slu/jobba-pa-slu/ Placering: Umeå Anställningsform: Tillsvidareanställning. SLU kan komma att tillämpa provanställning. Omfattning: 100% Tillträde: Enligt överenskommelse. Ansökan: Välkommen med din ansökan via ansökningsknappen nedan senast 2026-08-10. Fackliga kontaktpersoner: https://internt.slu.se/min-anstallning/facket/kontaktpersoner/   Sveriges lantbruksuniversitet (SLU) har en nyckelroll i utvecklingen för hållbart liv, grundad i vetenskap och utbildning. Genom vårt fokus på samspelen mellan människa, djur och ekosystem och ett ansvarsfullt brukande av naturresurserna bidrar vi till en hållbar samhällsutveckling och goda livsvillkor på vår planet. Huvudorter är Alnarp, Umeå och Uppsala, men verksamhet bedrivs också på forskningsstationer, försöksparker och utbildningsorter i hela landet. SLU har drygt 4000 medarbetare, 6000 studenter och forskarstuderande och en omsättning på över 4,5 miljarder kronor. Universitetet satsar på attraktiva miljöer på sina campusområden. Vi arbetar för en jämställd och inkluderande arbetsmiljö där öppna samtal mellan människor med olika erfarenheter lägger grunden för vetenskaplighet, kreativitet och utveckling. Vi välkomnar därför personer med olika bakgrunder och perspektiv att söka den aktuella anställningen.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Upstream Field Application Specialist at Cytiva is responsible for delivering product demonstrations, advanced hands‑on training and consulting to customers. This role is part of the Bioprocess Customer Application Support team based in Europe, supporting customers across EMEA, and is a remote position. At Cytiva, our vision is to advance future therapeutics from discovery to delivery. What you will do: Support the sales process by advising during sales discussions, delivering presentations, and performing hands‑on cell culture demonstrations for Cytiva’s upstream product portfolio, including Xcellerex™ XDR and X‑platform, WAVE™ bioreactor systems, and the ReadyToProcess™ (RTP) platform. Deliver advanced post‑installation training and consulting to customers, providing application support for bioreactor users. This includes process optimization, process transfer to Cytiva’s single‑use bioreactors, and expert technical support such as troubleshooting and extended on‑site, process‑connected problem solving. Provide input to Marketing, R&D, and Management, with a strong focus on customer feedback, market insights, and competitor practices. You will contribute ideas for technical improvements, new solutions, processes, and unit operations, and deliver industrially focused training in cell culture, bioreactors, and applications for Cytiva colleagues, as needed. Participate in and support global initiatives in education, consulting, and technical support. This includes preparing and executing standard and custom courses, delivering lectures and hands‑on lab training, and contributing to the development and continuous improvement of course materials and practical exercises. Who you are: You hold a university degree in Life Sciences (MSc or equivalent) and have at least 3 years of experience in upstream processing within a large‑scale industrial environment. You bring experience from research, development, and manufacturing within pharma, biopharma, or biotech, with a strong focus on cell culture and bioreactors. You have extensive hands‑on bioreactor experience at an expert level, preferably with single‑use bioreactors and mammalian cells, including experience in cell culture process development and scale‑up. Travel, Motor Vehicle Record & Physical/Environment Requirements: You are willing and able to travel up to 70%, primarily within Europe. You are fluent in English, and knowledge of at least one additional European language is preferred. It would be a plus if you also possess previous experience in: Hands-on experience of Cytiva’s Upstream product range Experience with single-use mixers We review applications on an ongoing basis and look forward to hearing from you. Apply today—we’re excited to learn more about you. Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com.

Postdoktor (2 år) inom cellväggens dynamik och mechanokemisk signalering Institutionen för fysiologisk botanik (Umeå universitet, Umeå Plant Science Centre, Sverige) välkomnar sökande till en postdoktoranställning inom cellväggens dynamik och mechanokemisk signalering. Förväntat startdatum är september 2026 eller enligt överenskommelse. Projektbeskrivning och arbetsuppgifter Vi söker en motiverad postdoktor för att medverka i DYNAMO-projektet ("Dynamics of Mechanochemical Signals in Plant Cell Walls") vid Plant Cell Wall Dynamics Lab, som leds av biträdande professor Laura Bacete. Projektet finansieras av Novo Nordisk Foundation (Emerging Investigator 2026 in Plant Science, Agriculture and Food Biotechnology). I projektet undersöks hur växter uppfattar och tolkar det fysikaliska och kemiska tillståndet i sina cellväggar, och hur dessa tillståndssignaler styr tillväxt, differentiering och stressrespons. Den framgångsrika kandidaten kommer att fokusera på att avgöra huruvida väggtillstånd sprider sig mellan vävnader, och hur denna spridning hänger samman med aktiv avkänning snarare än passiv mekanisk spridning. Optogenetiska och inducerbara genetiska verktyg kommer att användas för att generera definierade störningar av pektinremodelleringen, och Brillouinmikroskopi i kombination med levande-cell-signalreportrar kommer att användas för att karakterisera den vävnadsnivårespons som dessa störningar ger upphov till. Arbetet utförs i Arabidopsis thaliana, med utvalda förhållanden validerade i hybridasp, i nära samarbete med experter inom optisk mikroskopi, växtförsvar och syntetisk biologi. Behörighet och kvalifikationer För att anställas med stöd av avtal om tidsbegränsad anställning som postdoktor krävs avlagd doktorsexamen eller utländsk examen som bedöms motsvara doktorsexamen. Detta behörighetskrav ska vara uppfyllt senast vid tidpunkten då anställningsbeslutet fattas. För att anställas med stöd av postdoktoravtalet bör främst den komma ifråga som har avlagt examen enligt föregående stycke för högst tre år sedan. Om det finns särskilda skäl kan den komma i fråga som avlagt doktorsexamen tidigare. Med särskilda skäl avses ledighet på grund av sjukdom, föräldraledighet, förtroendeuppdrag inom fackliga organisationer, tjänstgöring inom totalförsvaret, eller andra liknande omständigheter samt klinisk tjänstgöring eller för ämnesområdet relevant tjänstgöring/uppdrag. Doktorsexamen ska vara inom växtbiologi, bioteknik, biofysik eller ett relaterat område. För denna anställning söker vi en person med starkt intresse för växtbiologi och entusiasm för att utveckla nya experimentella tillvägagångssätt.  Dokumenterad expertis inom cellväggsbiologi hos växter, innefattande kunskap om cellväggens sammansättning, remodelleringsenzymer och deras reglering. Praktisk erfarenhet av biokemisk karakterisering av cellväggsprotein, inklusive enzymatiska aktivitetsassays (t.ex. metylesteras- eller acetylesterasassays). Gedigen kompetens inom molekylär- och cellbiologiska tekniker, innefattande kloning (t.ex. GoldenGate eller Gateway), växttransformation och reporterlinjestrategier. Erfarenhet av proteinuttryck och rening och/eller optogenetik, i synnerhet tillämpad på reglering av enzymer för cellväggssyntes eller -remodellerig. Erfarenhet av konfokalmikroskopi och kvantitativ bildanalys i växtsystem. Mycket goda kunskaper i engelska i tal och skrift. Meriter Vi förväntar oss inte att den utvalda kandidaten är kunnig inom samtliga av följande från början, men vederbörande bör vara angelägen om att lära sig de tekniker som krävs. Följande anses meriterande: Erfarenhet av olika modellväxter, inklusive Arabidopsis thaliana. Kännedom om signalvägar kopplade till cellväggsintegritet, innefattande receptorliknande kinasnettverk eller tillhörande nedströms kaskader. Kunskaper i beräkningsbiologi, biologisk modellering och/eller biostatistik. Deltagande i vetenskapskommunikation och utåtriktad verksamhet. På det personliga planet söker vi en god lagspelare som också kan arbeta självständigt när det krävs. Vi vill att du: Kan organisera och strukturera ditt arbete. Levererar resultat enligt gjorda överenskommelser. Är proaktiv och tar egna initiativ. Är beredd att dela med dig av dina kunskaper till praktikanter och juniora medlemmar i forskargruppen. Om anställningen Anställningen är på heltid under två år, med möjlighet till förlängning om maximalt ett år beroende på projektets framsteg. Lön och anställningsvillkor fastställs i enlighet med Umeå universitets kollektivavtal. Den utsedde forskaren kommer att få fullt stöd från PI för att utveckla sin egen forskningsprofil, skriva ansökningar om anslag samt följa en individuell meriteringsplan utarbetad tillsammans med PI. Anställningen startar i september 2026 eller enligt överenskommelse. Ansökan Du ansöker via vårt rekryteringssystem Varbi senast den 31 juli 2026. Dokument ska skickas elektroniskt, i MS Word- eller PDF-format, via rekryteringssystemet. Ansökan ska vara skriven på engelska (företrädesvis) eller svenska och ska innehålla: Motiveringsbrev (max 2 sidor). Kort forskningsbeskrivning (1 sida) där du diskuterar dina forskningsintressen, t.ex. när du först intresserade dig för området, vilka kunskaper du har förvärvat hittills, vilka forskningsfrågor du finner mest angelägna, och vilka dina långsiktiga karriärmål är. CV med fullständig publikationslista. Styrkta kopior av examensbevis och intyg från högre utbildning. Kopia av publikationer (om sådana finns) och doktorsavhandling. Kontakt Om du har frågor om anställningen, vänligen kontakta Laura Bacete (laura.bacete@umu.se). Vänligen ställ dina frågor på engelska. Institutionen för fysiologisk botanik värdesätter de egenskaper som en jämn könsfördelning tillför institutionen, och därför uppmuntrar vi särskilt kvinnor att söka anställningen.  Vi ser fram emot din ansökan!

Are you passionate about quality, contamination control, and medical device manufacturing? We are looking for a Cleanliness & Sterility Assurance Engineer to join our team and support the cleanliness and sterility assurance of dental implant products manufactured at our sites in Karlskoga, Sweden, and Yorba Linda, USA. In this role, you will play a key part in ensuring compliance with regulatory requirements and industry standards while contributing to the safety and quality of products that improve patients' lives worldwide. Key Responsibilities As a Cleanliness & Sterility Assurance Engineer, you will: Define validation studies related to microbiological, physical, and chemical cleanliness for new equipment and equipment modifications. Lead and execute cleanliness process validations for new and updated manufacturing equipment. Develop and implement cleanliness monitoring activities in collaboration with the Contamination Control Manager. Maintain and update contact material mapping documentation. Establish and maintain procedures, templates, and best practices to ensure standardized cleanliness validation and monitoring processes. Support biological and microbiological safety strategies across the organization. Coordinate and manage external testing activities with approved laboratories and vendors when required. Collaborate with cross-functional teams to support continuous improvement and regulatory compliance initiatives. Qualifications and Experience To succeed in this role, you should have: A Master's degree (MSc) or equivalent in Biotechnology, Biomedical Engineering, Microbiology, Toxicology, Biology, Chemistry, or another relevant scientific discipline. At least 5 years of experience within the Medical Device industry or a comparable regulated environment. Strong knowledge of contamination control, cleanliness assurance, and applicable regulatory standards, or the ability to quickly develop expertise and work independently with limited supervision. Experience with relevant standards such as ISO 13485 and ISO 11137-1 & 2. A solid understanding of manufacturing processes and process validation methodologies. Strong expertise in statistical analysis and interpretation of technical data. Excellent communication skills, both written and verbal. Fluency in English. Swedish language skills are considered an advantage. A structured, analytical, and problem-solving mindset.

The role We call ourselves a 60-year-old startup. Decades of scientific heritage, paired with the speed, ambition and hands-on energy of a company being built from the ground up. Right now, we're scaling manufacturing fast, and that means the way we assure sterility needs to scale with it. We're looking for a Sterility Assurance Lead who wants to own that agenda from day one, not just maintain a system, but shape how sterility assurance grows alongside the site. You will own and drive the site’s sterility assurance strategy. This role ensures compliance with global regulatory requirements and serves as the SME for contamination control, aseptic processing, and sterilization validation. Key Responsibilities Lead the Sterility Assurance Program (SAP) and Contamination Control Strategy (CCS) in line with EU GMP Annex 1 and global standards. Oversee environmental monitoring, cleanroom qualification, and aseptic practices. Review sterilization validations and lead media fill programs. Drive contamination risk assessments, investigations, and CAPAs. Act as SME during audits and inspections. Provide training and mentorship in sterility assurance best practices. The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week. Your Profile You are a highly motivated sterility assurance professional with a strong quality mindset and a passion for patient safety. You combine deep technical expertise with leadership capabilities and are comfortable acting as a site Subject Matter Expert. You're energized rather than unsettled by a fast-scaling environment, you bring a proactive, solution-oriented approach that lets you spot risks early, drive improvements, and push operational excellence forward even as priorities shift. You thrive in a collaborative, cross-functional environment and can communicate complex technical topics clearly to both technical and non-technical stakeholders. You're confident leading investigations, mentoring colleagues, and driving initiatives that strengthen contamination control and aseptic manufacturing performance, and you see this growth phase as a chance to grow your own scope right along with it. Requirements Bachelor's or Master's degree in Microbiology, Biotechnology, Pharmacy, or another relevant life science discipline. 8–12 years of experience in sterile manufacturing, microbiology, or sterility assurance within the pharmaceutical, biologics, or medical device industry. Proven experience working in GMP-regulated environments and supporting regulatory inspections and audits. Hands-on experience with contamination control strategies, environmental monitoring programs, and aseptic manufacturing operations. Skills Deep technical expertise in aseptic processing, sterilization technologies (moist heat, dry heat, filtration), and microbial contamination control. Strong knowledge of cleanroom operations, HVAC qualification, isolators/RABS, and environmental monitoring systems. Solid understanding of EU GMP Annex 1 requirements and familiarity with global regulatory expectations (FDA, EMA, PIC/S). Experience performing risk assessments using tools such as FMEA, HACCP, or similar methodologies. Strong analytical mindset with the ability to interpret data trends and drive continuous improvement initiatives. Excellent documentation skills and a structured approach to problem-solving and investigations. Strong communication and collaboration skills with the ability to influence cross-functional teams. Application If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application. About Galderma Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

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

At Intervacc, we are pioneering the next generation of veterinary vaccines through our proprietary technology platform. Rooted in research from the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), our mission is to reduce the impact of bacterial infections in animals through innovative, effective, and safe vaccines. Our first proprietary product — a vaccine against strangles, a serious streptococcal infection in horses— is now available in several European markets. This is just the beginning. We are expanding our reach into new territories and broadening our product portfolio. We have an exciting new opportunity for an experienced CMC Lead who will be responsible for the manufacturing and testing for the company’s marketed products, as well as the CMC-strategy for development of new vaccine products. The CMC Lead will have a central role in providing scientific guidance, support, and expertise for all CMC activities including commercial products and product under development. You will work with products in different markets to fulfill a key role within our dedicated, friendly and experienced team. If this sounds interesting to you – come join us! Intervacc AB is headquartered in Stockholm Sweden and is listed on the Swedish Nasdaq First North Growth Market. The position is full-time, and we welcome your application today! Key responsibilities As a CMC Lead, you will provide CMC strategy and expertise for our development and marketed products to ensure the company’s products are developed, manufactured, tested and maintained in compliance with global regulatory expectations, requirements and guidance. Duties and responsibilities include: Responsibility of delivering CMC-parts of development projects, launch projects as well as projects/products in commercial phase Developing CMC-strategies and ensuring oversight and planning of work performed at CROs/CMOs related to development, analytical testing and manufacturing of products Monitor KPIs and ensure timely delivery of data to support development, manufacturing and release Being responsible and promote using modern processing analytical principles such as Quality by Design, risk-based method development and data-driven decision making. Working with other internal functions as well as external suppliers and partners to ensure CMC-deliverables and resolve arising issues Participating in budget planning and monitoring Ensure compliance with global regulatory requirements and support regulatory inspections and audits Skills and Competencies The suitable candidate has the following qualifications: Formal academic degree level (MSc., Ph.D) in a science-related subject e.g. pharmacy, biology or chemistry Significant experience (more than 7-10 years) in development, manufacturing and analytical testing of biologics or biotechnology-derived products e.g. vaccines from the pharmaceutical industry Significant knowledge of the drug development and manufacturing process for biologics (including upstream and downstream processes and analytical methods) Expert knowledge in analytical and/or process development for biologics Understanding of supply planning and supplier management Knowledge of current regulatory CMC requirements, and solid knowledge in understanding of regulations and guidance for the manufacturing of biotechnology products Excellent communication and documentation skills in English are required The successful candidate for this position will be someone who: Has a solid scientific background with significant experience in processing and analytical testing of biotechnology products in combination with project management skills Is analytical, solution-oriented with a strong personal drive Is structured and organized Has a good eye for detail and a thorough approach to work Is a proactive, flexible, motivated and ambitious team player with ability to drive change If you are ready to bring your expertise within the CMC area for biologics, we are ready to offer you an excellent career opportunity at an innovative company with an exciting journey ahead! About Intervacc: Intervacc is an innovative Swedish biotechnology company that develops and markets modern, effective, and safe vaccines against bacterial infections affecting animals. Over the past decade, advances in molecular biology techniques have significantly enhanced our ability to investigate the genomes of pathogenic bacteria. Building on our research foundations at the Karolinska Institute (KI) and the Swedish University of Agricultural Sciences (SLU), we have developed a technology platform for a new generation of vaccines. Our first proprietary vaccine, a vaccine against the streptococcal infection strangles, which affects horses—is now available in several European markets. The Intervacc share (STO: IVACC) is listed on the NASDAQ First North Growth Market and our headquarter is in Stockholm, Sweden. You can find more information about Intervacc at www.intervacc.se For more information about this position, please contact: Krishan Johansson Haque, PhD Sr Recruitment Consultant, QRIOS Life Science & Engineering T: +46 (0)72-070 16 53 E: krishan.johansson-haque@qrios.se

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products. As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us! This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today. Key responsibilities The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO. Duties and responsibilities include: Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency. Lead root cause investigations and implement corrective and preventive actions (CAPA). Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification. Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results. Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why. Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles. Support audits and inspections by customers, regulatory authorities, and Notified Bodies. Support technology transfers from R&D to production and participate in cross-functional development projects. Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply. Skills and Competencies The suitable candidate has the following qualifications: Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related. Strong background in process engineering preferably combined with validation engineering experience. Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries). Experience with process optimization, process validation and problem solving. Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable. Experience working with Quality Management Systems. Knowledge of statistical analysis and process capability concepts. Excellent communication and documentation skills in English are required The successful candidate for this position will be someone who: Has a strong technical and analytical mindset. Enjoys solving complex manufacturing and process-related challenges. Is structured and detail-oriented. Takes ownership and drives improvements independently. Communicates effectively across departments and organizational levels. Combines hands-on problem solving with a systematic approach. Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important. We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development. About Bohus Biotech Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence. With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide. Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas: Ophthalmology – OVD solutions supporting tissue protection during cataract surgery Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform Orthopaedics – Injectable treatments for osteoarthritis All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com For more information about this position, please contact: Krishan Johansson Haque, PhD Sr Recruitment Consultant, QRIOS Life Science & Engineering T: +46 (0)72-070 16 53 E: krishan.johansson-haque@qrios.se

Department for Molecular Sciences Subject area: Biology Description of the PhD projects We are seeking two PhD students in the field of biogas production, with a focus on the digestion process. The biogas process is currently an important tool for achieving multiple societal benefits and environmental goals. Through anaerobic digestion, a wide range of organic waste streams and residues can be treated while simultaneously closing nutrient cycles and producing renewable energy and nutrient-rich biofertilizers. Biogas production also contributes to increased preparedness and self-sufficiency. The biogas process is driven by complex microbial communities that must remain balanced to ensure efficient and stable biogas production. At the Department of Molecular Sciences, research is conducted both on process operation and optimization and on process microbiology, often in close integration. The PhD projects will focus on the following areas, with some opportunity for the successful candidates to influence the detailed project design. Biogas production from agricultural feedstocks – Process optimisation. Biogas production in the agricultural sector is currently expanding rapidly, creating a strong need for new knowledge and technological development. As a PhD student in this project, you will operate and evaluate different laboratory-scale biogas processes with the aim of optimising both biogas production and biofertiliser quality. The processes will be studied using chemical and microbiological analyses, and there will also be opportunities to work with process modelling. Process microbiology. This project focuses on the microbiology of different types of biogas processes and on how microbial activity is affected by different operational conditions, as well as how these changes relate to process function and stability. The work will involve molecular biological methods and bioinformatics to analyse microbial communities in both laboratory-scale and full-scale biogas processes. The aim is to identify microorganisms and microbial markers associated with specific operating conditions and to be used to predict process disturbances. Qualifications: A Master's degree in biology, microbiology, biotechnology, molecular biotechnology, bioinformatics, or a related field. Excellent knowledge of English, both written and spoken (equivalent to a passing grade in Swedish upper secondary school English B/English 6). Your profile: We are seeking highly motivated candidates with a strong commitment to advancing renewable energy systems and a keen interest in biotechnology and industrial microbiology. Applicants should be able to read and critically evaluate scientific literature in English and communicate effectively in both written and spoken English. Excellent communication and teamwork skills are essential. Meritorious qualifications: Knowledge and experience in one or more of the following areas are considered an advantage: Biogas processes, Modelling and/or programming, statistics, Swedish language skills About us: The positions are based at the Department of Molecular Sciences at the Swedish University of Agricultural Sciences (SLU) in Uppsala, Sweden. For more information about the department, please visit our website: https://www.slu.se/en/departments/molecular-sciences/ The positions are connected to the national transdisciplinary centre of excellence, the Biogas Solutions Research Center (BSRC), as well as the Interreg project BEAR for the PhD project 1, carried out in collaboration with Luleå University of Technology and the University of Oulu. BSRC brings together researchers from Linköping University and SLU, together with approximately 50 private and public organizations representing the entire biogas value chain. The PhD positions within BSRC are intended to promote co-production of knowledge between academia, industry, and the public sector, thereby ensuring long-term competence development in both research and industry. Both projects will be carried out within the Microbial Biotechnology research group, and the principal supervisor for both projects will be Professor Anna Schnürer. The PhD students will also be supervised by additional researchers within the research group, ensuring access to the expertise required for the successful completion of the projects. Since the projects are conducted in close collaboration with industry and other societal stakeholders, the supervisory teams may also include external supervisors from industry. Read more about our benefits and what it is like to work at SLU: https://www.slu.se/en/about-slu/work-at-slu/ Read more about doctoral studies at SLU: https://www.slu.se/en/education/programmes-courses/doctoral-studies/ Employment and salary: The position is a full-time doctoral studentship comprising four years of postgraduate education. Salary is determined according to the local collective agreement for doctoral students, with fixed salary progression levels. Scope: 100 % av heltid Location: Uppsala Start date: Upon agreement but not later than December 2026 Application and selection: Please submit your application using the link below not later than 2026-08-31. Applicants are welcome to apply for one or both PhD positions. The application must clearly state which project(s) are being applied for, indicate which project is the applicant's first priority, and explain the reasons for this choice. 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/min-anstallning/facket/kontaktpersoner/

Overview På QIAGEN drivs vi av en enkel men kraftfull vision: att göra förbättringar i livet möjliga. Vi är dedikerade till att revolutionera vetenskap och sjukvård till det bättre. Från våra entreprenöriella rötter till vår nuvarande globala närvaro har vi vuxit till en kraft för positiv förändring. Med tusentals anställda på sex kontinenter är samarbete vår största styrka. Vi strävar alltid efter att identifiera begåvade individer som kan ansluta sig till våra exceptionella team. Vi har spelat en central roll i att forma modern vetenskap och sjukvård, och vi har bara börjat. Om du är någon som trivs med nya utmaningar, värdesätter mångfald och vill göra en påtaglig skillnad i människors liv, då är QIAGEN rätt plats för dig. På QIAGEN är varje dag en möjlighet att göra skillnad i verkliga livet. Gå med oss, väx med oss och låt oss tillsammans forma framtiden för biologiska upptäckter. About the opportunity Join QIAGEN DNA Synthesis (QDS) in Västerås as a Development Engineer within our Technology Development & Process Excellence (TD/PE) team. This role offers the opportunity to contribute to cutting-edge advancements in analytical and preparative liquid chromatography, supporting the development of premium quality oligonucleotides to our customers. Working within a collaborative and multidisciplinary team, you will play a key role in developing methods, techniques and processes to ensure an optimised, best in class oligonucleotide production process. You will operate in a dynamic environment where continuous improvement, scientific curiosity, and ownership are highly valued. Your tasks Developing and optimising analytical and preparative liquid chromatography methods (e.g. HPLC, UPLC, LC-MS) for oligonucleotide production Planning, executing, and evaluating development projects related to oligonucleotide manufacturing processes Defining project scope, timelines and deliverables, and communicating progress to internal and external stakeholders Supporting deviation investigations and CAPA activities in collaboration with Quality Assurance Contributing to continuous process improvement initiatives to enhance quality, efficiency and robustness Creating, reviewing and maintaining SOPs and electronic lab documentation Providing support to the onsite oligonucleotide production facility as required Your profile Please submit your application in English We are looking for someone whose drive and mindset match their skills - someone who sees challenges as opportunities. Work can be fast paced, so we’re looking for someone who brings energy, ownership and a growth mentality to both TD/PE and QDS. Bachelor’s or Master’s degree in subject areas related to Chemistry, Chemical Engineering, Biotechnology, Biochemistry or equivalent. Hands-on experience with analytical and preparative liquid chromatography (e.g. UPLC, HPLC, LC-MS). A theoretical and practical knowledge of solid-phase oligonucleotide/peptide and/or organic synthesis. Ability to write, review and follow SOPs related to oligonucleotide synthesis, as well as writing and reviewing electronic lab journals. Familiarity of working in regulated environments such as ISO9001, ISO13485 and/or cGMP standards would be advantageous. Experience of working with process development initiatives would be advantageous. An advanced ability to communicate in verbal and written formats in both English and Swedish is essential as the language onsite is Swedish. What we offer Extra pensionsförmån Hälsobidrag (2500 kr/år) Volontärens dag Möjlighet att gå med i interna QIAGEN-gemenskaper Prestationsrelaterad bonus Hybridarbete (villkorat av din roll) Vårt folk är hjärtat i allt vi gör. Passion driver oss när vi tänjer på gränser för att förnya och utvecklas. Vi inspirerar med vårt ledarskap och påverkar med våra handlingar. Vi odlar en samarbetande, stödjande miljö där varje individ och team kan blomstra. Vi kämpar för ansvarsskyldighet och uppmuntrar entreprenöriellt tänkande.  QIAGEN är engagerad i att skapa en mångfaldig miljö och är stolta över att vara en arbetsgivare med lika möjligheter. Alla kvalificerade sökande kommer att få övervägande för anställning utan hänsyn till ras, hudfärg, kön, ålder, nationellt ursprung, religion, sexuell läggning, könsidentitet, status som veteran eller funktionshinder.

Hansa Biopharma develops innovative treatments that give patients with rare and serious immune-mediated conditions a chance to a better life. We are now looking for an experienced Senior QA Manager Validation and Quality, to help shape our quality work at one of the most exciting biotech companies in the Nordics. About the role You will be a key player in a QA team of six dedicated colleagues, all based at our office in Lund. As Senior QA Manager, you will drive and approve validation activities - spanning process, cleaning and analytical method validation - with a clear quality perspective. You will act as subject matter expert supporting cross-functional teams, external partner management and regulatory authority inspections. This is the right role for you if you thrive with both strategic ownership and operational presence - where one day you are reviewing validation documentation and the next you are in dialogue with a CDMO or preparing a team for an authority inspection. Your responsibilities: Provide strategic and operational direction for quality management and validation across development, clinical and commercial manufacturing QA review and approval of validation documentation Supplier quality management: guide and qualify external manufacturing partners (CDMOs/CMOs) throughout the product lifecycle Support authority inspections and internal/external audits of suppliers and vendors Cross-functional collaboration with CMC, Regulatory, Clinical and Supply Chain Drive continuous improvement of the Quality Management System (QMS) and proactively identify areas for development Who are you? We believe you are a seasoned QA professional with broad experience across both drug substance (DS) and drug product (DP) manufacturing. You are thorough and results-oriented, but also a natural collaborator who knows when to take the lead and when to seek input from others. We are looking for someone with: Advanced degree (Ph.D. or M.Sc.) in Chemical Engineering, Chemistry, Pharmaceutical Sciences or a related discipline 10+ years of biopharmaceutical industry experience with a focus on QA, process development and validation Proven track record of leading validation activities for DS and DP through clinical and commercial stages Strong knowledge of aseptic manufacturing and biotechnology processes Deep understanding of regulatory requirements (FDA, EMA, ICH) related to manufacturing and validation Experience managing external partners and CDMOs/CMOs Experience of authority inspections (FDA, EMA) as presenter and/or coordinator Strong communication skills and the ability to influence across functions and organisational levels What we offer At Hansa, you will not just have a job - you will have a role where your work directly contributes to changing lives for patients with acute and complex immune disorders. A close-knit, welcoming culture in a mid-sized company where you can see how your contribution makes a difference The opportunity to help build a fully integrated biopharmaceutical company with global reach Talented, driven colleagues with an open and entrepreneurial mindset A strong pipeline built on Hansa’s proprietary IgG-cleaving enzyme technology platform Office in Lund, at the heart of a vibrant Life Science ecosystem Our values At Hansa, we are guided by our core values: Accountability, Courage, Integrity and Pioneering. We believe in the power of diversity and are committed to building an inclusive workplace where every perspective is valued. Appealing? Send in an application as soon as possible. In this recruitment, Hansa Biopharma is collaborating with SallyQ. For questions, please contact Ellinor Crafoord, Senior Recruitment Consultant, +46793554257 or ellinor.crafoord@sallyq.se.

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/

Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry. Assignment Description We are looking for a Senior IT Infrastructure Specialist What You Will Work On Execute IT infrastructure migration activities as part of a large global integration project. Perform Active Directory domain migrations and user migrations. Replace, configure, deploy, and support Windows laptops for end users. Install, configure, and troubleshoot Windows 10 and Windows 11 enterprise devices. Support Microsoft 365 services and enterprise workplace technologies. Manage endpoint deployment and administration using Intune, SCCM, Microsoft Autopilot, or similar solutions. Provide technical support for LAN, Wi-Fi, VPN, printers, meeting rooms, and peripheral devices. Troubleshoot user access issues, permissions, MFA, Single Sign-On (SSO), and corporate applications. Support onboarding activities for new ERP, business, and corporate systems. Work within structured ITSM processes using platforms such as ServiceNow. Produce and maintain technical documentation and support change management activities. Collaborate with local users, global IT teams, and project stakeholders throughout the migration lifecycle. Support IT operations across office, laboratory, and light manufacturing environments. Ensure stable, secure, and efficient workplace IT services during migration and transition activities. What You Bring Senior-level experience in IT infrastructure and enterprise IT operations. Proven experience with Active Directory, domain migrations, and user migration projects. Strong knowledge of Microsoft 365, Windows 10, Windows 11, and enterprise desktop environments. Experience with laptop replacement, client deployment, installation, configuration, and end-user support. Hands-on experience with endpoint management solutions such as Microsoft Intune, SCCM, Microsoft Autopilot, or equivalent. Good understanding of enterprise networking, including LAN, Wi-Fi, VPN, printers, meeting room technology, and peripheral devices. Experience troubleshooting authentication, permissions, Multi-Factor Authentication (MFA), Single Sign-On (SSO), and enterprise applications. Experience supporting onboarding and migration to ERP, business, or corporate systems. Familiarity with ITSM platforms such as ServiceNow and structured incident, request, and change management processes. Strong documentation skills and understanding of IT change management. Experience from Life Science, pharmaceutical, biotechnology, laboratory, or manufacturing environments is highly desirable. Excellent communication skills in both Swedish and English. Self-driven, hands-on, and comfortable working directly with end users as well as global IT teams. Strong analytical, troubleshooting, and problem-solving skills. Ability to work effectively in complex enterprise environments with multiple stakeholders.

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.