Search results for "cell culture"

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

Om uppdraget 🔬 Du kommer att ingå i ett Bioscience Immunology-team inom Research and Early Development, Respiratory & Immunology. Rollen fokuserar på in vitro-studier och ex vivo-analyser av musceller med inriktning mot inflammatoriska och autoimmuna sjukdomar. Området Respiratory & Immunology är ett av organisationens kärnterapiområden och har som mål att förstå, behandla, modifiera och i förlängningen bota respiratoriska och autoimmuna sjukdomar. Uppdraget passar dig som vill arbeta nära forskningen, bidra till läkemedelsutveckling och vara delaktig i att generera robusta, publicerbara vetenskapliga resultat. Dina arbetsuppgifter 🔍 I rollen planerar, genomför och analyserar du in vitro- och ex vivo-experiment som stödjer läkemedelsutvecklingsprojekt. Du bidrar aktivt i vetenskapliga diskussioner kring studiedesign och tolkning av data samt presenterar resultat, slutsatser och rekommendationer i projekt- och teamforum. Arbetet är praktiskt och hands-on, där du utför analyser kopplade till prekliniska studier i nära samarbete med andra forskare. Du ansvarar för att säkerställa högsta kvalitet vad gäller dataintegritet, kvalitetssäkring och arkivering samt för att sammanställa rapporter och vetenskapliga sammanfattningar. Din profil / Obligatoriska kompetenser ✅ Masterexamen i biologi eller närliggande område Minst 5 års erfarenhet av flödescytometri (FACS) på musmaterial, inklusive organpreparering, digestion, färgning och antikroppspaneldesign God vana av BD FACSDiva-instrument och analys i FlowJo Förmåga att självständigt planera, genomföra och analysera proteinanalyser såsom ELISA, Western blot och Meso Scale Discovery Erfarenhet av RNA-arbete inklusive extraktion och qRT-PCR Förståelse för statistik, datakvalitet, rapportering och arkivering Mycket god engelska i tal och skrift samt stark presentationsförmåga Meriterande färdigheter ⭐ Doktorsexamen inom immunologi Djup förståelse för autoimmuna sjukdomar, särskilt inom mag-, hud- eller ledimmunologi Erfarenhet av in vivo-modeller för inflammation och autoimmunitet Erfarenhet av cellisolering och cellsortering, exempelvis MACS, StemCell Technologies och FACS-baserad sortering Erfarenhet av cellodling och in vitro-assays med murina leukocyter Personliga egenskaper 🤝 Du är analytisk, noggrann och har ett starkt vetenskapligt driv. Du trivs med praktiskt laboratoriearbete men uppskattar också att diskutera data och slutsatser i grupp. Du arbetar strukturerat, tar stort ansvar för kvalitet och leverans och har lätt för att kommunicera komplexa resultat på ett tydligt sätt. Språk 🌍 Mycket god engelska i tal och skrift. Plats: Göteborg Omfattning: Heltid, 100 % Period: 2026-03-16 – 2026-12-31 Sista ansökningsdag: 15 mars 2026 Sway Sourcing är en innovativ rekryteringspartner som specialiserar sig på att matcha rätt talang med rätt företag – snabbt och effektivt. Vårt huvudfokus ligger inom Ekonomi, Administration, HR, Marknad och IT, men vi har även den breda expertis och flexibilitet som krävs för att leverera skräddarsydda rekryteringslösningar inom alla branscher. Trots att vi är en relativt ny aktör har vi redan byggt förtroende hos många av Sveriges största företag och arbetar både nationellt och internationellt. Med baser i Sverige och Spanien erbjuder vi en unik kombination av lokal expertis och global räckvidd. Vårt starka nätverk och djupa branschinsikter gör oss till en självklar partner för företag som vill ligga steget före i sin rekrytering.

Do you want to contribute to top quality medical research? We invite applications for a Research Assistant position in the research group of Professor Magnus Ingelman-Sundberg, within the Section of Pharmacogenetics.   This position is housed in the Department of Physiology and Pharmacology, known for its collegial, international, and dynamic research environment. Our current research focuses on the use CYP2C19 is a highly polymorphic enzyme involved in the metabolism of many drugs and endogenous lipids, making it one of the most clinically important pharmacogenes. Beyond drug metabolism, CYP2C19 regulates lipid pathways influencing vascular function, inflammation, cholesterol homeostasis, and broader metabolic processes. We will investigate why fetal CYP2C19 expression induces inflammation in the developing hippocampus, leading to neuronal degeneration in the adult dentate gyrus causing anxiety and depression in adult life identifying molecular pathways relevant for future antidepressant development. Reduced CYP2C19 function has been associated with increased risk of myocardial infarction and ischemic stroke, suggesting broader roles in cardiovascular disease. Using advanced human liver spheroids and brain organoids, we will study CYP2C19 in lipid metabolism ini relation to cardiovascular risk, by identifying CYP2C19-dependent lipid pathways providing new insights into mechanisms underlying neuropsychiatric disorders and arteriosclerosis.   Your profile We are seeking a motivated candidate with at least one year of hands-on laboratory experience and practical skills in RT-PCR, Western blotting, and cell culture. Experience in immunohistochemistry, imaging techniques, and molecular biology methods is highly desirable. Previous work with brain tissues is a merit. You will join a dynamic research team of approximately six researchers and contribute to several ongoing projects focused on the biological functions of CYP2C19. Your primary responsibilities will include: · Analysis of lipids regulated by CYP2C19 using advanced 3D human liver spheroids as an experimental model. · Characterization of developmental alterations in the fetal brain caused by CYP2C19 overexpression using approaches such as immunohistochemistry, RNA sequencing, and ELISA. · Development and use of in vitro macrophage activation systems to investigate whether CYP2C19-dependent lipid mediators promote inflammatory pathways relevant to atherosclerosis and cardiovascular disease. While knowledge of the Swedish language is advantageous, fluency in both oral and written English is essential. The successful candidate will be a team player with excellent communication skills, well-organized, and enjoy interacting with researchers and students.   What We Offer Karolinska Institutet is one of the world's leading medical universities. Our vision is to advance knowledge about life and promote better health for all. At Karolinska Institutet, we conduct successful medical research and offer the largest range of medical education in Sweden. As a state university, we provide numerous benefits through our collective agreement, including access to modern wellness facilities with trained staff on-site. Location: Solna, Biomedicum MIS-lab : https://ki.se/en/people/magnus-ingelman-sundberg#about-me We look forward to your application!   The application is to be submitted through the Varbi recruitment system. In this recruitment, you will apply with your CV without a personal letter. Instead, you will answer some questions about why you are applying for the job in the application form. Want to make a difference? Join us and contribute to better health for all Type of employment: Temporary position, 1 year Contract type: Full time First day of employment: According to agreement Salary: Monthly salary City: Stockholm Country: Sweden Contact: Magnus Ingelman-Sundberg, magnus.ingelman-sundberg@ki.se

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

About CCRM Nordic CCRM Nordic breaks down the bottlenecks that slow life-changing therapies from lab to patient. Based at GoCo Health and Innovation City in Mölndal, we provide ATMP teams across Sweden, the Nordics and Europe with the infrastructure, know-how and partner network they need, whether that means a single consultation or a long-term manufacturing collaboration. We have invested in a brand-new GMP manufacturing facility with five processing rooms on floor 16 of GoCo House. We are now building the founding team that will shape how this facility runs, and are looking for a Manufacturing Team Lead ready to be part of something genuinely exciting. The opportunity This is a founding role. As one of the first hires into the manufacturing team, you will help build the structure, not just step into it. From authoring SOPs and batch records to training operators and leading quality investigations, this role sits at the operational heart of CCRM Nordic's manufacturing capability. You will lead a team of up to six GMP operators across multiple processing rooms, manage day-to-day scheduling and training, and act as the department's SME for quality systems. You will work alongside PD and MSAT colleagues on new product introductions and technology transfers, and collaborate with our Validation team on equipment qualification and process establishment. Key responsibilities Manufacturing Operations Lead day-to-day GMP manufacturing operations across multiple processing rooms, ensuring clinical materials are delivered on time and to the highest quality standard. Perform and oversee hands-on processing including cell culture, bioreactor operation, Tangential Flow Filtration (TFF) and chromatography. Schedule and manage housekeeping, environmental monitoring and cleaning activities, internally and with external contractors. Maintain full inventory control, ensuring consumables and raw materials are stocked and within expiry. People & Team Leadership Line manage a team of up to six pharmaceutical operators, including performance management, workload planning and day-to-day support. Design and deliver training plans to ensure every team member is qualified for all processing and ancillary activities. Act as a role model for a collaborative, high-performance culture: mentoring and developing the people around you. Quality & Compliance Serve as the manufacturing SME for all GMP quality matters, leading incident investigations, root cause analyses, change controls and CAPAs. Ensure all operations are executed in strict accordance with approved SOPs, Batch Manufacturing Records and current GMP guidelines. Author and review SOPs, batch records, logbooks, COSHH assessments and User Requirement Specifications for new equipment. Support regulatory inspections and ensure the facility is always inspection-ready. Collaborate with the Validation Department on equipment calibration, qualification and shutdown planning. New Product Introduction & Tech Transfer Partner with PD and MSAT teams to introduce new products and processes into the GMP suite. Support technology transfers into and out of the facility, including handovers to clients or CMOs. What we are looking for Essential Minimum 5 years' GMP manufacturing experience, with a strong focus on bioproduction or ATMPs. Proven track record as a line manager of a GMP manufacturing team. Hands-on experience with ATMPs, ideally including Viral Vectors or similar advanced modalities. Degree in bioprocessing, microbiology or a related life science discipline, or equivalent experience. Deep working knowledge of GMP QMS systems: quality incidents, change controls and CAPA management. Experience authoring SOPs, batch records and validation documentation. Strong communication skills and ability to collaborate across functions. Highly Desirable Experience in Tech Transfer and process validation. Hands-on operation of TFF systems, including Repligen platforms. Experience supporting or participating in regulatory inspections. The person We are looking for someone who is: A strong team player who invests in the people around them and understands that great manufacturing is a collective achievement. Adaptable and calm under pressure, able to pivot when processes change, timelines shift or unexpected challenges arise. Energised, not overwhelmed, by the complexity of a new facility and evolving product portfolio. Service-oriented and delivery-focused, with high personal standards for accuracy and thoroughness. An excellent organiser who can hold multiple priorities without letting quality slip. Why join CCRM Nordic? CCRM Nordic is an innovation-led organisation at the frontier of ATMP development. Joining now means helping to shape the team, culture and operational standards of a facility that will directly contribute to getting advanced therapies to patients faster. A rare opportunity to join a founding manufacturing team and leave your mark on how things are built. Work alongside world-class scientists and process development experts on cutting-edge ATMP programmes. A collaborative, supportive environment where your expertise is genuinely valued. Clear pathways for growth as the team expands from Phase 1 through to full multi-project manufacturing capacity. Competitive salary in line with the Swedish pharmaceutical market. Ready to build something important? We'd love to hear from you.

The Senior Cell Design Engineer will lead the design and development of current and next-generation lithium-ion battery cells, supporting both product innovation and customer programs. The role is responsible for defining cell design strategies, executing development projects, and driving technical solutions from concept to commercialization Key Responsibilities Overall areas of responsibilities and activities Lead the design and development of lithium-ion battery cells for ESS, EV, and other applications. Develop and optimize cell architecture, electrode design, and material selection to achieve performance, energy density, lifetime, and cost targets. Define development strategies and DOE to support cell development and validation activities. Evaluate cell performance, reliability, and manufacturability through testing, analysis, and data-driven development. Support scale-up activities and ensure design compatibility with manufacturing processes. Lead technical development projects and coordinate cross-functional activities across R&D, manufacturing, quality, and program teams. Serve as the primary technical interface for customers and support customer development programs from concept to qualification. Drive battery development roadmaps and deliver project milestones aligned with customer and business requirements Requirements Educational background and previous experience required for the role Qualifications and Experience ​​• PhD or MSc in chemical engineering/Electrochemistry/chemistry/material science and engineering  •  Minimum 3 years of experience in the automotive industry. •  Minimum 8 years of experience in lithium-ion battery cell design and development • Extensive experience on cell design and development of Li-ion cells   •  Extensive experience in battery prototyping, validation, and scale-up activities •  Working knowledge of lithium-ion battery manufacturing and mass production processes • Working experience with OEM project for Li-ion battery cell/module business   •  Experience leading technical activities for customer-facing development programs • Strong background from technical culture and proven engineering excellence​  Specific skills ​Strong knowledge of lithium-ion battery materials, electrode design, and cell architecture. Experience with DOE, statistical analysis, and data-driven development methodologies. Excellent project management and technical problem-solving skills. Strong communication skills in English, both written and verbal. Ability to work effectively under tight timelines and changing priorities. Personal success factors Strong leadership and decision-making skills. Ability to drive technical development activities and deliver project milestones. Excellent collaboration and stakeholder management capabilities. Results-oriented mindset with a focus on quality and execution. Strong analytical and problem-solving skills. Ability to thrive in a fast-paced, international environment

About Norvion Systems AB Headquartered in Gothenburg, Sweden, Norvion Systems AB is an innovative engineering company dedicated to deploying cutting-edge AI, robotics, and embedded systems solutions across the Nordic region and Europe. We bridge advanced technological innovation with successful real-world deployments, serving as Europe’s trusted engineering partner. Our leadership and core technical teams comprise industry veterans and technical experts from global tech pioneers, Tier 1 suppliers, and intelligent cockpit fields. We cultivate a practical, reliable, and quality-driven Nordic engineering culture. At Norvion, you will work at the forefront of Embodied AI and advanced edge platform engineering, collaborating with top-tier research institutions and industrial leaders to push the limits of technology. The Opportunity: To support our partner’s advancements in automotive electrification, we are currently looking for a Battery Cell Test Engineer – Durability for an exciting engineering assignment in Gothenburg. This is a premier opportunity for engineers passionate about Li-ion battery technology, testing, durability, and the future of green mobility. The role perfectly combines hands-on laboratory work with advanced data analysis and cross-functional collaboration. 🎯 Key Focus Areas Test Coordination: Planning and coordinating comprehensive battery cell durability and performance tests. Data Analysis & Modeling: Analyzing complex test data using Python, MATLAB, Excel, or similar analytical tools. Ageing & Lifecycle Analysis: Supporting battery life prediction, degradation mechanisms, and cell ageing analysis. Cross-Functional Collaboration: Collaborating closely with internal laboratories, global suppliers, and core engineering teams. Methodology Optimization: Contributing to the development of new test methods and driving continuous laboratory improvements. 👤 Profile & Qualifications We are looking for an analytical and motivated engineer with a background in battery technology or laboratory validation: Testing Experience: Proven experience in battery cell testing, laboratory validation, or hardware verification. Data Skills: Strong proficiency in using Python, MATLAB, or Excel for technical data analysis. Educational Background: A degree in Electrochemistry, Materials Science, Mechanical, Electrical, Chemical Engineering, or a related field. Soft Skills: A strong analytical mindset with excellent communication and documentation skills in English. Work Authorization: The legal right to work in Sweden by the project start date (or possessing an active permit allowing an immediate start without a new application process) is required due to the September 2026 timeline. Nice to have (Bonus Skills): Prior experience in automotive electrification or working with battery test rigs. Deep knowledge of battery durability, cell chemistry, and degradation modes. 🎁 Why Choose Norvion? A Stage to Push Boundaries: "Engineering Beyond Boundaries" — We provide direct, hands-on exposure to the future of advanced automotive systems, general-purpose robotics, and embodied intelligence. Work with Tech Experts: Collaborate closely with a highly skilled engineering team boasting deep European delivery experience. No red tape, just pure engineering excellence. Nordic Work Culture: Embrace a flexible, flat, and results-oriented environment that values work-life balance and individual growth.

The University of Gothenburg tackles society's challenges with diverse knowledge. 58 000 students and 6800 employees make the university a large and inspiring place to work and study. Strong research and attractive study programmes attract researchers and students from around the world. With new knowledge and new perspectives, the University contributes to a better future. https://web103.reachmee.com/ext/I005/1035/job?site=7&lang=UK&validator=9b89bead79bb7258ad55c8d75228e5b7&job_id=39310 Subject area Single-cell genomics and functional imaging of kidney epithelial injury Subject area description The project aims to develop and apply novel experimental methods to study functional heterogeneity in proximal tubular epithelial cells (PTECs) during kidney injury. By combining direct measurements of albumin reabsorption with single-cell transcriptomics, the project seeks to identify molecular programs underlying epithelial dysfunction and to discover targetable pathways relevant to kidney disease. Duties The successful candidate will lead experimental work across multiple PTEC injury models, including toxic, metabolic, inflammatory, and hypoxia–reoxygenation stress. Key tasks include functional uptake assays using fluorescently labelled albumin, cell and tissue imaging, preparation of single-cell RNA sequencing libraries, data generation from primary human PTECs and acute kidney slices, and close collaboration with computational researchers for downstream analysis. Validation of candidate pathways in tissue slices will be an additional component of the work. Eligibility The eligibility criteria for employing teaching staff are set out in Chapter 4 of the Higher Education Ordinance and in the Appointment Procedure for Teaching Posts at the University of Gothenburg. To be eligible for appointment as a postdoc, the applicant is required to have a doctoral degree, a doctoral degree in art or a foreign degree that is deemed to be equivalent to a doctoral degree. This eligibility requirement must be met before the employment decision is made. In the first instance, those who have completed their degree no more than three years prior to the end of the application period shall be considered. Those who have completed their degree more than three years prior to the end of the application period may also be considered in the first instance if special grounds exist. Special grounds relate to leave of absence due to illness, parental leave, commissions of trust within union organisations, service within the defence services or other similar circumstances, as well as clinical service or service/assignment relevant to the subject area. Assessment criteria The ideal candidates should have: PhD in Molecular or Cell Biology, or a related life science discipline Experience in cell-based assays and tissue culture Experience with molecular biology techniques (RNA extraction, qPCR, NGS library preparation) Experience with microscopy techniques, and analysis tools (e.g. Fiji) Knowledge of single-cell RNA sequencing methods Experience with functional assays in epithelial cells or kidney-related models Experience with FACS Experience analyzing high-dimensional biological data (Python) Ability to work independently, plan experiments, and troubleshoot High level of motivation, accuracy, and organizational skills Fluency in English Regulations for the evaluation of qualifications for academic positions are given in Chapter 4, Section 3 - 4 of the Higher Education Ordinance Employment The employment is full time and temporary, two years with the possibility of one year's extension, with placement at the Institute of Biomedicine. First day of employment as agreed. Selection process https://www.gu.se/en/work-at-the-university-of-gothenburg/how-to-apply-for-a-position Contact information If you have any questions about the position, please contact Dr. Joan Camuñas Soler: joan.camunas@gu.se Unions Union representatives at the University of Gothenburg can be found here: https://www.gu.se/om-universitetet/jobba-hos-oss/hjalp-for-sokande Application Submit your application via the University of Gothenburg's recruitment portal by clicking the "Apply" button. It is your responsibility to ensure that the application is complete as per the vacancy notice, and that the University receives it by the final application deadline. The application should contain: A short statement describing the candidate's training, interests and future goals as well as motivation to apply for this position. Curriculum Vitae Proof of completed PhD Contact details of two references Applications must be received by: 2026-08-14. Information for International Applicants Choosing a career in a foreign country is a big step. Thus, to give you a general idea of what we and Gothenburg have to offer in terms of benefits and life in general for you and your family/spouse/partner please visit: https://www.gu.se/en/about-the-university/welcome-services https://www.movetogothenburg.com/ The University works actively to achieve a working environment with equal conditions, and values the qualities that diversity brings to its operations. Salaries are set individually at the University. In accordance with the National Archives of Sweden's regulations, the University must archive application documents for two years after the appointment is filled. If you request that your documents are returned, they will be returned to you once the two years have passed. Otherwise, they will be destroyed. In connection to this recruitment, we have already decided which recruitment channels we should use. We therefore decline further contact with vendors, recruitment and staffing companies.

Software Engineer – CellaVision Join CellaVision and help shape the future of digital cell morphology. After years of research and innovation, CellaVision is ready to take the next step in digital cell morphology. Do you want to be part of CellaVision’s newest venture, working with cutting-edge technologies to develop one of the key diagnostic tools in cancer care? If so, this is your opportunity to join CellaVision. About CellaVision CellaVision is the global leader in digital cell morphology within hematology, and our analyzers are used in healthcare laboratories around the world. We operate at the forefront of technology, applying the latest advances in software development, digital imaging, and machine learning to create real value for our customers. www.cellavision.com About the Role We are looking for a versatile engineer who enjoys working in a dynamic environment where research meets product development. You are curious, hands-on, and comfortable moving between exploratory work and the structure needed to turn ideas into robust products. You adapt quickly to changing priorities and new challenges, and you thrive in a setting where not everything is fully defined from the start. You enjoy solving complex problems, collaborating across disciplines, and contributing wherever needed to move the product and team forward. You value teamwork, take ownership of your work, and can balance innovation with quality and delivery. As a Software Engineer in CellaVision, your work will include: Working across the full development spectrum, from research-oriented exploration to product-ready implementation Contributing to feature development using technologies such as C++, C# and Python Developing and refining algorithms within digital imaging Applying and further developing methods within AI and machine learning Reviewing code, hunting bugs, and optimizing performance Collaborating across disciplines to solve complex problems and adapt solutions as product and research needs evolve Contributing to software design and architecture for robust, scalable solutions Taking part in building new ways of working in a team operating in a fast-moving and evolving technical area Utilizing AI tools to speed up software development Our Offer At CellaVision, you will be part of an innovative and international environment with a company culture that encourages collaboration, initiative, and the execution of great ideas that create customer value. We also offer: Flexible working hours and reduced working hours to support work–life balance Secure employment covered by a collective agreement, including insurance, occupational pension, parental leave supplements, and more A strong focus on wellbeing and health, including: Free gym at the office Wellness allowance Lunch benefit Sponsored running events Discounts on gym memberships A modern office designed to support collaboration and a healthy work environment A team-oriented culture where we enjoy working together and meeting for weekly breakfasts About You You have experience in product development, from prototype through to production. You understand the value of teamwork and are comfortable breaking down complex challenges into manageable parts that can be solved effectively within a team setting. You remain calm and structured in demanding situations, and you have a strong ability to prioritize and focus on what matters most. Your Background We believe you have: An M.Sc. in Engineering or a related field Experience in product development involving software and Machine Learning Experience working as a software developer Experience in the design and implementation of software architecture Experience in computer vision and digital imaging Strong communication skills in English, both written and spoken Care to Join? This is a full-time position based at CellaVision HQ in Lund, Sweden, in our modern offices with excellent infrastructure and commuting options. We are looking to fill the position as soon as possible. In this recruitment process, we are partnering with Radeptus. For any questions regarding the position, please contact Jenny Månsson at +46 703 318 506 or via email at jenny@adeptus.se. Please submit your application here. We do not accept applications via email.

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 Manager, Global Service Readiness Engineering — CIBP is responsible for leading a team of service readiness engineers that ensures service readiness across the Cell & Gene Therapy (Sepax, Sefia, Xuri), Biacore, Imager, and Palltronics product portfolios — some of Cytiva's highest-revenue and most strategically important product lines. This role combines people leadership with hands-on service engineering expertise to deliver high-quality service deliverables on time across New Product Development (NPD) projects and Lifecycle Management (LCM) activities. This position reports to the Director, Global Service Engineering & Equipment Intelligence and is part of the Global Service Readiness Engineering organization located in Uppsala, Sweden or Portsmouth, UK and will be a onsite role. What you will do: Lead and develop a team of service readiness engineers — including hiring, onboarding, training, performance management, career development discussions, and establishing a regular cadence of 1:1s and staff meetings. Oversee and prioritize daily operations of the CIBP engineering team to ensure on-time delivery (OTD) and high quality of all service deliverables across NPD tollgates and LCM activities (~180 LCM tasks/month organization-wide). Drive service readiness in NPD projects — owning DFS (Design for Serviceability) scoring, Service Support Plans, EHS Risk Assessments, and spare parts (FRU) strategies for assigned product platforms at all tollgate stages. Manage lifecycle activities including service documentation updates, field modifications, engineering change orders, calibration procedures, and spare parts updates in collaboration with Service Operations, R&D, and Manufacturing. Act as Subject Matter Expert (SME) on all service aspects relating to the assigned CIBP product portfolio, serving as the primary interface between central functions (R&D, Manufacturing, QA) and regional service teams. Who you are: Bachelor's degree in Engineering, Life Sciences, Physics, or a related technical field — or equivalent combination of education and experience. Multiple years of relevant work experience in service engineering, field service, or product development within the life sciences or medical device industry. Demonstrated experience leading or supervising technical teams, including hiring, onboarding, performance management, and talent development. Experience working in cross-functional NPD or product lifecycle project teams, meeting tollgate deadlines and delivering against defined specifications. Working knowledge of quality management systems (e.g., ISO 13485, GMP/GxP, Veeva QMS) and design control processes. Fluency in English (written and spoken); Swedish language skills are a plus. It would be a plus if you also possess: Experience with PDM/PLM systems (e.g., Magic/Windchill) Familiarity with Danaher Business System (DBS) tools and methodologies Field service experience with bioprocess, chromatography, or analytical instruments

Job Scope Why does the role exist? High level purpose of function. The Senior Manufacturing Engineer plays a key role in process equipment commissioning, production ramp-up, and full-scale manufacturing within a battery cell production facility. They ensure smooth start-up of production lines, optimize manufacturing processes, and lead continuous improvement initiatives to maximize process yield, equipment availability, and overall production performance. This role combines hands-on equipment commissioning experience, cross-functional collaboration, and technical expertise to deliver safe, efficient, and high-quality battery cell production. A Senior Manufacturing Engineer is responsible for all aspects of their process machine including technical functionality, how personnel interact with it, what maintenance activities are recommended and what crucial spares are required. Key Responsibilities Overall areas of responsibilities and activities Key responsibilities include (but are not limited to) Participate in HAZOP (Hazard & Operability Study) sessions and ensure compliance with process safety, operational safety, and environmental standards.  Promote a culture of safety, quality, and operational excellence throughout production and commissioning activities.  Lead process equipment commissioning, including cold and hot commissioning on-site during start-up or restart projects. (Project timeline dependent)  Facilitate smooth transitions from commissioning to production ramp-up and full-scale manufacturing. (Project timeline dependent)  Translate lessons learned into design and process improvements for future expansions.  Monitor, analyze and improve production KPIs, including yield, availability, and performance. Identifying top losses, production bottlenecks, and performance gaps to drive corrective actions and continuous improvement initiatives.  Lead root cause analysis (RCA) for equipment-related losses, minor stops, and process deviations.  Define, release, and maintain manufacturing process standards and operator training programs.  Train and mentor new engineers, operators and other support functions.  Prepare, review, and approve documentation including (but not limited to WI, PFMEAs, commissioning checklists, project timelines, A3s).   Provide technical feedback and guidance to suppliers to ensure equipment quality, compliance with specifications, and CE standards.  Develop and issue DOEs (Design of Experiments) and schedule process and equipment trials onsite and at supplier sites (if required).  Deliver a line capable of obtaining PPAP approval, following a structured quality gate model.   Guide and mentor colleagues to industrial best practices, focusing on growth and development.  Complete supplementary tasks as seen fit by management to effectively utilize time and resource for the benefit of the business.  This role requires regular presence on the production floor. Requirements Educational background and previous experience required for the role Qualifications and Experience Master's degree in mechanical, electrical, or chemical engineering.  Minimum of 7 years of relevant work experience in production, equipment, or engineering-related roles.  Proven track record of leading manufacturing process improvements and production optimization in a factory environment following recognised project management techniques.   Experience in building and scaling production in a fast-growing environment, ideally within the battery, food, pharma, paper & pulp, semiconductor, electrochemical, or similar industries.  Hands-on experience and interest in equipment commissioning, troubleshooting, and optimisation.  Proficient in detailed root cause analysis, structured problem-solving methodologies and continuous improvement.  Familiarity with quality assurance troubleshooting tools.  Experience working to industry standards obtaining certification including ISO, IATF &VDA.  Experience with statistical process control and process capability analysis. Experience working with preventive maintenance strategies and Total Productive Maintenance (TPM) concepts within a production environment. Experience in spare part prioritisation and stock optimisation, balancing equipment availability with cost efficiency. Specific skills & Knowledge Strong knowledge of mechanical, electrical, hydraulic, and pneumatic systems.  Knowledge of OEE (Overall Equipment Effectiveness) metrics and their application in production environments.  Knowledge of lean manufacturing principles and six sigma methodologies.  Highly autonomous with a proactive mindset and work ethic.   Strong technical curiosity, analytical mindset, and business-oriented problem-solving skills.  Troubleshooting skills with diagnostic equipment. Ability to document technical problems concisely.  Proficient in the use of a Computerised Maintenance Management System (CMMS) for work order management, equipment data, and maintenance reporting. Experience with Microsoft Dynamics 365 is advantageous. Experience in coaching, upskilling, and mentoring engineers or technicians, with a demonstrable commitment to developing the technical capability of others within a production 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.  Ability to work within varying environments including clean-rooms and dry-rooms, while wearing appropriate PPE.  Comfortable operating in high-profile, international, and high-pressure environments.  A genuine technical interest and passion about working within production is highly valued.

Job Scope Why does the role exist? High level purpose of function. The Senior Manufacturing Engineer plays a key role in process equipment commissioning, production ramp-up, and full-scale manufacturing within a battery cell production facility. They ensure smooth start-up of production lines, optimize manufacturing processes, and lead continuous improvement initiatives to maximize process yield, equipment availability, and overall production performance. This role combines hands-on equipment commissioning experience, cross-functional collaboration, and technical expertise to deliver safe, efficient, and high-quality battery cell production. A Senior Manufacturing Engineer is responsible for all aspects of their process machine including technical functionality, how personnel interact with it, what maintenance activities are recommended and what crucial spares are required. Key Responsibilities Overall areas of responsibilities and activities Key responsibilities include (but are not limited to) Participate in HAZOP (Hazard & Operability Study) sessions and ensure compliance with process safety, operational safety, and environmental standards.  Promote a culture of safety, quality, and operational excellence throughout production and commissioning activities.  Lead process equipment commissioning, including cold and hot commissioning on-site during start-up or restart projects. (Project timeline dependent)  Facilitate smooth transitions from commissioning to production ramp-up and full-scale manufacturing. (Project timeline dependent)  Translate lessons learned into design and process improvements for future expansions.  Monitor, analyze and improve production KPIs, including yield, availability, and performance. Identifying top losses, production bottlenecks, and performance gaps to drive corrective actions and continuous improvement initiatives.  Lead root cause analysis (RCA) for equipment-related losses, minor stops, and process deviations.  Define, release, and maintain manufacturing process standards and operator training programs.  Train and mentor new engineers, operators and other support functions.  Prepare, review, and approve documentation including (but not limited to WI, PFMEAs, commissioning checklists, project timelines, A3s).   Provide technical feedback and guidance to suppliers to ensure equipment quality, compliance with specifications, and CE standards.  Develop and issue DOEs (Design of Experiments) and schedule process and equipment trials onsite and at supplier sites (if required).  Deliver a line capable of obtaining PPAP approval, following a structured quality gate model.   Guide and mentor colleagues to industrial best practices, focusing on growth and development.  Complete supplementary tasks as seen fit by management to effectively utilize time and resource for the benefit of the business.  This role requires regular presence on the production floor. Requirements Educational background and previous experience required for the role Qualifications and Experience Master's degree in mechanical, electrical, or chemical engineering.  Minimum of 7 years of relevant work experience in production, equipment, or engineering-related roles.  Proven track record of leading manufacturing process improvements and production optimization in a factory environment following recognised project management techniques.   Experience in building and scaling production in a fast-growing environment, ideally within the battery, food, pharma, paper & pulp, semiconductor, electrochemical, or similar industries.  Hands-on experience and interest in equipment commissioning, troubleshooting, and optimisation.  Proficient in detailed root cause analysis, structured problem-solving methodologies and continuous improvement.  Familiarity with quality assurance troubleshooting tools.  Experience working to industry standards obtaining certification including ISO, IATF &VDA.  Experience with statistical process control and process capability analysis. Experience working with preventive maintenance strategies and Total Productive Maintenance (TPM) concepts within a production environment. Experience in spare part prioritisation and stock optimisation, balancing equipment availability with cost efficiency. Specific skills & Knowledge Strong knowledge of mechanical, electrical, hydraulic, and pneumatic systems.  Knowledge of OEE (Overall Equipment Effectiveness) metrics and their application in production environments.  Knowledge of lean manufacturing principles and six sigma methodologies.  Highly autonomous with a proactive mindset and work ethic.   Strong technical curiosity, analytical mindset, and business-oriented problem-solving skills.  Troubleshooting skills with diagnostic equipment. Ability to document technical problems concisely.  Proficient in the use of a Computerised Maintenance Management System (CMMS) for work order management, equipment data, and maintenance reporting. Experience with Microsoft Dynamics 365 is advantageous. Experience in coaching, upskilling, and mentoring engineers or technicians, with a demonstrable commitment to developing the technical capability of others within a production 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.  Ability to work within varying environments including clean-rooms and dry-rooms, while wearing appropriate PPE.  Comfortable operating in high-profile, international, and high-pressure environments.  A genuine technical interest and passion about working within production is highly valued.

Job Scope Why does the role exist? High level purpose of function. The Manufacturing Engineer plays a key role in process equipment commissioning, production ramp-up, and full-scale manufacturing within a battery cell production facility. They ensure smooth start-up of production lines, optimize manufacturing processes, and lead continuous improvement initiatives to maximize process yield, equipment availability, and overall production performance. This role combines hands-on equipment commissioning experience, cross-functional collaboration, and technical expertise to deliver safe, efficient, and high-quality battery cell production. The manufacturing engineer is responsible for all aspects of their process machine including technical functionality, how personnel interact with it, what maintenance activities are recommended, and what crucial spares are required.   Key Responsibilities Overall areas of responsibilities and activities Key responsibilities include (but are not limited to) Participate in HAZOP sessions and ensure compliance with process safety, operational safety, and environmental standards.  Promote a culture of safety, quality, and operational excellence throughout production and commissioning activities.  Lead process equipment commissioning, including cold and hot commissioning on-site during start-up or restart projects. (Project timeline dependent)  Facilitate smooth transitions from commissioning to production ramp-up and full-scale manufacturing. (Project timeline dependent)  Translate lessons learned into design and process improvements for future expansions.  Monitor, analyze and improve production KPIs, including yield, availability, and performance. Identifying top losses, production bottlenecks, and performance gaps to drive corrective actions and continuous improvement initiatives.  Lead root cause analysis (RCA) for equipment-related losses, minor stops, and process deviations.  Define, release, and maintain manufacturing process standards and operator training programs.  Train and mentor new engineers, operators and other support functions.  Prepare, review, and approve documentation including (but not limited to); WI, PFMEAs, commissioning checklists, project timelines, A3s.   Provide technical feedback and guidance to suppliers to ensure equipment quality, compliance with specifications, and CE standards.  Develop and issue DOEs (Design of Experiments) and schedule process and equipment trials onsite and at supplier sites (if required).  Deliver a line capable of obtaining PPAP approval, following a structured quality gate model.  Complete supplementary tasks as seen  fit by management to effectively utilize time and resources for the benefit of the business.  This role requires regular presence on the production floor. Requirements Educational background and previous experience required for the role Qualifications and Experience Bachelor’s degree in mechanical, electrical, or chemical engineering.  Minimum of 3 years of relevant work experience in production, equipment, or engineering-related roles.  Proven track record of leading manufacturing process improvements and production optimization in a factory environment following recognised project management techniques.   Experience in building and scaling production in a fast-growing environment, ideally within the battery, food, pharma, paper and pulp, semiconductor, electrochemical, or similar industries.  Hands-on experience and interest in equipment commissioning, troubleshooting, and optimisation.  Proficient in detailed root cause analysis, structured problem-solving methodologies and continuous improvement.  Familiarity with quality assurance troubleshooting tools.  Experience working to industry standards obtaining certification including ISO, IATF &VDA . Experience with statistical process control and process capability analysis.  Experience working with preventive maintenance strategies and Total Productive Maintenance (TPM) concepts within a production environment. Experience in spare part prioritisation and stock optimisation, balancing equipment availability with cost efficiency. Specific skills & Knowledge Strong knowledge of mechanical, electrical, hydraulic, and pneumatic systems.  Knowledge of lean manufacturing principles and six sigma methodologies . Knowledge of OEE (Overall Equipment Effectiveness) metrics and their application in production environments.  Strong technical curiosity, analytical mindset, and business-oriented problem-solving skills.  Troubleshooting skills with diagnostic equipment.  Ability to document technical problems concisely. Proficient in the use of a Computerised Maintenance Management System (CMMS) for work order management, equipment data, and maintenance reporting. Experience with Microsoft Dynamics 365 is advantageous. 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.  Ability to work within varying environments including clean-rooms and dry-rooms, while wearing appropriate PPE.  Comfortable operating in high-profile, international, and high-pressure environments. A genuine technical interest and passion about working within production is highly valued.

Job Scope Why does the role exist? High level purpose of function. The Manufacturing Engineer plays a key role in process equipment commissioning, production ramp-up, and full-scale manufacturing within a battery cell production facility. They ensure smooth start-up of production lines, optimize manufacturing processes, and lead continuous improvement initiatives to maximize process yield, equipment availability, and overall production performance. This role combines hands-on equipment commissioning experience, cross-functional collaboration, and technical expertise to deliver safe, efficient, and high-quality battery cell production. The manufacturing engineer is responsible for all aspects of their process machine including technical functionality, how personnel interact with it, what maintenance activities are recommended, and what crucial spares are required.   Key Responsibilities Overall areas of responsibilities and activities Key responsibilities include (but are not limited to) Participate in HAZOP sessions and ensure compliance with process safety, operational safety, and environmental standards.  Promote a culture of safety, quality, and operational excellence throughout production and commissioning activities.  Lead process equipment commissioning, including cold and hot commissioning on-site during start-up or restart projects. (Project timeline dependent)  Facilitate smooth transitions from commissioning to production ramp-up and full-scale manufacturing. (Project timeline dependent)  Translate lessons learned into design and process improvements for future expansions.  Monitor, analyze and improve production KPIs, including yield, availability, and performance. Identifying top losses, production bottlenecks, and performance gaps to drive corrective actions and continuous improvement initiatives.  Lead root cause analysis (RCA) for equipment-related losses, minor stops, and process deviations.  Define, release, and maintain manufacturing process standards and operator training programs.  Train and mentor new engineers, operators and other support functions.  Prepare, review, and approve documentation including (but not limited to); WI, PFMEAs, commissioning checklists, project timelines, A3s.   Provide technical feedback and guidance to suppliers to ensure equipment quality, compliance with specifications, and CE standards.  Develop and issue DOEs (Design of Experiments) and schedule process and equipment trials onsite and at supplier sites (if required).  Deliver a line capable of obtaining PPAP approval, following a structured quality gate model.  Complete supplementary tasks as seen  fit by management to effectively utilize time and resources for the benefit of the business.  This role requires regular presence on the production floor. Requirements Educational background and previous experience required for the role Qualifications and Experience Bachelor’s degree in mechanical, electrical, or chemical engineering.  Minimum of 3 years of relevant work experience in production, equipment, or engineering-related roles.  Proven track record of leading manufacturing process improvements and production optimization in a factory environment following recognised project management techniques.   Experience in building and scaling production in a fast-growing environment, ideally within the battery, food, pharma, paper and pulp, semiconductor, electrochemical, or similar industries.  Hands-on experience and interest in equipment commissioning, troubleshooting, and optimisation.  Proficient in detailed root cause analysis, structured problem-solving methodologies and continuous improvement.  Familiarity with quality assurance troubleshooting tools.  Experience working to industry standards obtaining certification including ISO, IATF &VDA . Experience with statistical process control and process capability analysis.  Experience working with preventive maintenance strategies and Total Productive Maintenance (TPM) concepts within a production environment. Experience in spare part prioritisation and stock optimisation, balancing equipment availability with cost efficiency. Specific skills & Knowledge Strong knowledge of mechanical, electrical, hydraulic, and pneumatic systems.  Knowledge of lean manufacturing principles and six sigma methodologies . Knowledge of OEE (Overall Equipment Effectiveness) metrics and their application in production environments.  Strong technical curiosity, analytical mindset, and business-oriented problem-solving skills.  Troubleshooting skills with diagnostic equipment.  Ability to document technical problems concisely. Proficient in the use of a Computerised Maintenance Management System (CMMS) for work order management, equipment data, and maintenance reporting. Experience with Microsoft Dynamics 365 is advantageous. 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.  Ability to work within varying environments including clean-rooms and dry-rooms, while wearing appropriate PPE.  Comfortable operating in high-profile, international, and high-pressure environments. A genuine technical interest and passion about working within production is highly valued.

Job Scope Why does the role exist? High level purpose of function. The Manufacturing Engineer plays a key role in process equipment commissioning, production ramp-up, and full-scale manufacturing within a battery cell production facility. They ensure smooth start-up of production lines, optimize manufacturing processes, and lead continuous improvement initiatives to maximize process yield, equipment availability, and overall production performance. This role combines hands-on equipment commissioning experience, cross-functional collaboration, and technical expertise to deliver safe, efficient, and high-quality battery cell production. The manufacturing engineer is responsible for all aspects of their process machine including technical functionality, how personnel interact with it, what maintenance activities are recommended, and what crucial spares are required. Key Responsibilities Overall areas of responsibilities and activities Key responsibilities include (but are not limited to) · Participate in HAZOP sessions and ensure compliance with process safety, operational safety, and environmental standards. · Promote a culture of safety, quality, and operational excellence throughout production and commissioning activities. · Lead process equipment commissioning, including cold and hot commissioning on-site during start-up or restart projects. (Project timeline dependent) · Facilitate smooth transitions from commissioning to production ramp-up and full-scale manufacturing. (Project timeline dependent) · Translate lessons learned into design and process improvements for future expansions. · Monitor, analyze and improve production KPIs, including yield, availability, and performance. Identifying top losses, production bottlenecks, and performance gaps to drive corrective actions and continuous improvement initiatives. · Lead root cause analysis (RCA) for equipment-related losses, minor stops, and process deviations. · Define, release, and maintain manufacturing process standards and operator training programs. · Train and mentor new engineers, operators and other support functions. · Prepare, review, and approve documentation including (but not limited to); WI, PFMEAs, commissioning checklists, project timelines, A3s. · Provide technical feedback and guidance to suppliers to ensure equipment quality, compliance with specifications, and CE standards. · Develop and issue DOEs (Design of Experiments) and schedule process and equipment trials onsite and at supplier sites (if required). · Deliver a line capable of obtaining PPAP approval, following a structured quality gate model. · Complete supplementary tasks as seen fit by management to effectively utilize time and resources for the benefit of the business. · This role requires regular presence on the production floor. Accountability/Authorization · Budget responsibility: N · Direct reports: N · Work Environment responsibility: N 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 Bachelor’s or master’s degree in mechanical, electrical, or chemical engineering. Minimum of 3 years of relevant work experience in production, equipment, or engineering-related roles. Proven track record of leading manufacturing process improvements and production optimization in a factory environment following recognised project management techniques. Experience in building and scaling production in a fast-growing environment, ideally within the battery, food, pharma, paper & pulp, semiconductor, electrochemical, or similar industries. Hands-on experience and interest in equipment commissioning, troubleshooting, and optimisation. Proficient in detailed root cause analysis, structured problem-solving methodologies and continuous improvement. Familiarity with quality assurance troubleshooting tools. Experience working to industry standards obtaining certification including ISO, IATF &VDA . Experience with statistical process control and process capability analysis. Specific skills & Knowledge Strong knowledge of mechanical, electrical, hydraulic, and pneumatic systems. Knowledge of lean manufacturing principles and six sigma methodologies . Knowledge of OEE (Overall Equipment Effectiveness) metrics and their application in production environments. · Strong technical curiosity, analytical mindset, and business-oriented problem-solving skills. · Troubleshooting skills with diagnostic equipment. Ability to document technical problems concisely. 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. Ability to work within varying environments including clean-rooms and dry-rooms, while wearing appropriate PPE. Comfortable operating in high-profile, international, and high-pressure environments. A genuine technical interest and passion about working within production is highly valued.

Join one of the world’s oldest start-ups — and help power what comes next At Husqvarna Group, innovation has been part of the story since 1689. Today, we are reinventing how people care for forests, parks, gardens and construction environments — with robotics, battery systems, smart technologies and sustainable product platforms at the center of that journey. Our Battery Competence Center is where electrification becomes real product technology, and we are now strengthening the hardware team with a Senior Hardware Designer who knows BMS development in depth. About the role This is a senior, hands-on engineering role. You will take battery subsystem requirements and turn them into robust BMS hardware solutions together with system engineers, cell specialists, software engineers and manufacturing experts Your responsibilities Derive hardware requirements from battery subsystem requirements and translate them into practical design choices. Define BMS hardware architecture and functional blocks based on system architecture, requirements, standards and certification needs. Create schematics and PCB designs in OrCAD, including symbols, footprints and production-ready documentation. Define the BMS interfaces to the battery system and contribute to the optimal EE layout of the battery design. Select electronic and electrical components with the right balance of performance, safety, availability and manufacturability. Prepare manufacturing deliverables for PCBA production and support test, troubleshooting, verification and validation. Define AFE parameters, operating modes and BMS functions in close collaboration with cell experts, system engineers and software engineers. Specify the hardware–software interface together with the software team and ensure clear, structured technical documentation. The technical landscape You will work close to the product and close to the details. The role suits someone who enjoys circuit-level problem solving, knows the trade-offs in BMS hardware, and can move naturally between architecture, schematic design, PCBA realization, verification and cross-functional decision-making. Location Huskvarna or Jonsered in Sweden or Karlstein am Main in Germany. How we work We believe the best ideas happen when we’re connected. We spend most of our time together in the office, creating space for collaboration, creativity, and fast decision-making. This helps us maintain a strong culture, supports learning and development, and ensures everyone has access to the people and resources they need to thrive. What we believe you bring BSc or MSc in Electronics, Embedded Systems, Electrical Engineering or a related field. Minimum 6 years of relevant professional experience in electronics/hardware development. Documented experience in hardware design for Battery Management Systems — this is essential. Strong experience in circuit and PCBA design and the confidence to work independently in complex designs. Hands-on experience with AFEs, MCUs and BMS-related hardware architectures. At least 3 years of OrCAD experience for schematic and PCB design. Fluent English, both spoken and written. Why join Husqvarna Group? If you are a senior BMS hardware engineer who wants ownership, technical depth and the chance to influence products at scale, we would be happy to hear from you. You will join a global innovation leader with a strong engineering culture, exciting electrification challenges, international collaboration and real opportunities to influence products used by millions of customers worldwide. Application Does this sound interesting? Please apply as soon as possible, as we review applications on an ongoing basis. We do not accept applications via e-mail due to GDPR regulations. Please note that due to the holiday period, response might take longer than normal. For more information about the position, please contact – Alireza Ahadpour Shal, Senior Hardware Engineer, at Alireza.Ahadpour.Shal@husqvarnagroup.com For questions regarding the recruitment process, please contact Talent Acquisition Partner – Katarina Engberg at katarina.engberg@husqvarnagroup.com Processing of personal data When you send in your application we will process your personal data. In case we choose to proceed with your application, we will ask you to verify your identity before giving you a job offer. Further background checks may be conducted where relevant. For more information about how we process your personal data, who we may share it with and what rights you have, please see our privacy notice. If you aren’t chosen to proceed in the process, you will be informed of this at the latest when the position has been filled. Winning Through Culture We believe that business is ultimately about people, as a team, we win and grow together. Our culture is built on bold ideas, strong commitment, and a shared purpose, creating an environment where innovation thrives, people grow, and every contribution matters. Our culture is built on three core themes: Bold: We push boundaries, embrace challenges, and explore new possibilities. Dedicated: We put in the hard work, bring passion and resilience to every challenge we take on. Care: We support each other, consider the impact of our actions, and strive to make a lasting difference. Whether you’re starting your career or looking for the next big step, we offer a place where passion and purpose come together. Join us in shaping the future! Learn more about our culture here: https://www.husqvarnagroup.com/en/our-culture