Sökresultat för "Biomedicinare"

Join CTC - where ambition is high and one of the goals is to strengthen the Swedish infrastructure in the Life Sciences! We are growing and are now looking for an additional Medical Writer who wants to contribute to CTC’s continued journey. Are you an experienced Medical Writer (MW) who wants to use your expertise to drive CTC’s development? Then this is the opportunity for you! As a Medical Writer at CTC, you will be part of a team of four other MWs responsible for writing and quality-checking regulatory documents, primarily clinical study protocols and reports. The work alternates between individual tasks and teamwork. You will be part of various study-specific project teams responsible for initiating and managing clinical projects until the delivery of study results. These cross-functional project teams include professionals such as project managers, medical and scientific advisors, research nurses, doctors, statisticians, and more. Main responsibilities: To write clinical study protocols and clinical study reports in accordance with ICH E6, ICH E3, and/or ISO 14155, and coordinate the development and quality control processes of these documents, both internally and with our clients. To write other regulatory documents and texts such as summary of results, narratives, substantial amendments and responses to authorities. To coordinate and lead meetings, both internally and externally, and act as a point of contact for clients. To serve as a mentor to colleagues. Other tasks such as medical coding, writing abstracts and scientific articles, writing assignments related to safety reporting, and writing marketing documents may also be required. We are looking for a driven and experienced Medical Writer who truly enjoys writing and formulating scientific texts. To succeed in this role, you need to have the ability to quickly and efficiently interpret, summarize, and present large amounts of data. We require you to have at least 3 years of experience in medical writing, drug development, and clinical trials. Previous experience in consultancy work and an understanding of the customer perspective are also valued. As a person, you are communicative and enjoy collaborating with experts in various fields. You are flexible, works independently, and deliver within agreed timelines. CTC’s core values: Innovation, Community, Respect, Commitment, and Professionalism resonate with you. Required qualifications MSc in the life sciences field. At least 3 years of experience in medical writing, drug development, and clinical trials. Experience in leading meetings and coordinating complex and parallel deliveries within agreed timelines. Proficiency in using the Microsoft Office suite, especially Microsoft Word. Excellent ability to express yourself grammatically correctly and clearly in English, both spoken and written. Good knowledge of the Swedish language (spoken and written). Preferred qualifications A PhD in the life sciences field. Experience with Phase 2-3 trials. Experience with medical devices and/or advanced therapy medicinal products (ATMP), as well as knowledge of regulatory requirements related to these areas. Experience in writing eCTD module 2; Clinical and Non-Clinical overview/summary, Investigator’s Brochures (IBs), Annual Safety Reports (ASRs). At CTC, you will be covered by a collective agreement and offered benefits such as flexible working hours, wellness allowance, and generous vacation terms. You will have the opportunity to work in a knowledge-intensive environment in a company with short decision-making paths, with good professional development opportunities. The position is located at our office in Uppsala (hybrid work is possible). Full time (40 hours per week). If you have questions, contact Marit Wangheim (Director Medical Writing) marit.wangheim@ctc-ab.se Please submit your application no later than 17 August 2026. CTC Clinical Trial Consultants AB is a Clinical Research Organization (CRO) with operations in Uppsala, Stockholm, Linköping, and Gothenburg. As a CRO, we conduct clinical trials and investigations on behalf of the pharmaceutical and medtech industry and academic institutions. We offer a comprehensive full-service solution that includes all the services, activities, and deliverables required to successfully conduct a clinical trial— bringing new pharmaceuticals and products to patients. We currently conduct clinical studies across all phases of development, from Phase 0 through Phase IV. Most of our studies are carried out at our own research clinics, although we also collaborate with external clinical sites. We employ approximately 125 people, around half of whom work in clinical roles. Our headquarters are located in Uppsala.

På Unilabs kombinerar vi medicinskt kunnande med mänsklig omtanke. Genom vårt sätt att arbeta skapar vi ett tydligt kundvärde och patientvärde. Detta uppnår vi med hjälp av effektiv diagnostik, hög kvalitet och förstklassig service gentemot våra patienter och kunder. Vi har en gemensam vilja att ge bästa möjliga förutsättningar för god vård till varje enskild individ, och våra medarbetares kompetens, drivkraft och engagemang utgör en viktig del av det mervärde vi skapar för samhället i stort. VAD Som biomedicinsk analytiker hos oss arbetar du självständigt med stort eget ansvar samtidigt som du är en viktig del av ett engagerat och kompetent team. Dina huvudsakliga arbetsuppgifter består av att analysera prover och säkerställa att korrekta resultat levereras med hög kvalitet och i rätt tid. Du kommer också att vara delaktig i utvecklings- och förbättringsarbete, där du har möjlighet att påverka både arbetsmetoder och processer. Vi värdesätter kontinuerlig kompetensutveckling och investerar i våra medarbetares lärande och utveckling. Hos oss får du möjlighet att bredda din kompetens och arbeta med varierande arbetsuppgifter. Genom att utveckla mångsidiga medarbetare bygger vi starka team och skapar en arbetsmiljö präglad av samarbete, kunskapsutbyte och ett gemensamt ansvarstagande där vi stöttar varandra i det dagliga arbetet. VEM På Unilabs väger inställning lika tungt som kompetens. Vi tror därför att du som person har en stark personlig driftkraft och ett öppet och flexibelt sinne med en förmåga att hitta nya lösningar. Vi tror även att du är social, kommunikativ och har lätt för att samarbeta och tillföra arbetsglädje bland dina arbetskamrater. Vi ser också att du är ansvarsfull, jobbar strukturerat och är stresstålig och har stor förståelse för kundens krav och behov och hur resultaten av vårt arbete påverkar patienten. Du eftersträvar att uppfylla arbetslagets gemensamma kvalitets- och leveranskrav, men kan även arbeta ensam och ta egna beslut. Vi söker dessutom dig som: Är legitimerad biomedicinsk analytiker Behärskar svenska i tal och skrift. Är tekniskt intresserad då stora delar av produktionen är automatiserad. Erfarenhet inom allmän kemi, immun kemi, diffar eller dokumentstyrning/ kvalitetsarbete är meriterande. VAR Tjänsten är placerad i Stockholm på S:t Görans akutlaboratorium 24/7 där du kommer att vara schemalagd dag, kväll och helg. Du kommer att välkomnas som en i gänget där dina arbetskamrater består av biomedicinska analytiker, biologer, biomedicinare, molekylärbiologer, undersköterskor, laboratoriebiträden samt kemister och läkare. Vår dagliga verksamhet bedrivs med korta beslutsvägar och laganda som viktig grund, god sammanhållning och hög trivselfaktor. I denna tjänst får du möjlighet att utvecklas och lära dig mer om det du finner intressant samt välja din spetskompetens. Ansökan Tjänsten är en heltidsanställning där kvälls och helgtjänstgöring ingår. Vid intresse tar vi gärna emot din ansökan så snart som möjligt och vi kallar till intervju löpande. Vi tillämpar provanställning. Vi ser fram emot att lära känna dig! Unilabs AB är idag en ledande aktör inom radiologi och laboratoriemedicin och Sveriges största privata leverantör av röntgen, mammografi och laboratoriemedicin. Vi möter våra patienter och kunder på sjukhus, närakuter, primärvårdslaboratorier, våra egna fristående röntgenenheter och mottagningar. Det är en verksamhet med full fart i en lugn omgivning med stor variation. Av våra totalt 13 000 medarbetare i Europa, arbetar drygt 1,200 i Sverige. Läs gärna mer om oss på www.Unilabs.se Unilabs erbjuder tjänster inom laboratoriemedicin och bild- och funktionsdiagnostik till öppen och sluten sjukvård. Våra tjänster kännetecknas av hög kvalitet, säkerhet och service. Unilabs har idag ca 1300 medarbetare men vi växer ständigt. De största yrkesgrupperna är biomedicinska analytiker, röntgensjuksköterskor och läkare med specialistkompetens inom radiologi eller laboratoriemedicin. Att arbeta på Unilabs innebär att förstå att vårt jobb inte bara är att producera testresultat. Vi tillhandahåller verkliga, användbara svar för våra patienter och vårdgivare. Vårt arbete förändrar livet direkt till det bättre, vilket vi ser som ett fantastiskt privilegium och något värt att arbeta för.

At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby. About the role We are now looking for a Process Engineer. This team will consist of different competencies, such as biomedicine, biotechnique, validation, automation and mechatronic. You will be responsible for automation/mechatronic knowledge within the department. You will also be responsible for one of our manufacturing processes and drive the work with continues improvements. Whenever there is a question regarding automation/mechatronic from your colleagues you will be asked to help. This is a team with a lot of cross-functional collaborations and responsibilities with both internal and external stakeholders from a variety of countries. Key Responsibilities Developing and implementing new production processes Driving continuous improvements on existing processes in close collaboration with all production departments Ensuring that existing production is compliant for all our in-house production within the business area Process engineering will also work with our outsourced products and the assessment and approval of our suppliers’ processes in close collaboration with our Quality Assurance, Supply Chain and Product Development department. This is a permanent, full-time position based at our office in Gothenburg. Travel and work from other Vitrolife sites and contract manufacturers might be part of the position. Your Profile Bachelor or master’s degree in biomedicine, chemistry, biology, mechanic, automation or equivalent Experiences from working with quality standards and processes (ISO-13485, GMP) 5 years’ experience of automation/mechatronic work Fluent in Swedish and good knowledge in English both oral and written You are thorough, structured, can see the whole picture and are able to prioritize and meet deadlines. You are also service-oriented, solution-focused and communicative and you enjoy working in a changing and dynamic environment. Applications will be reviewed on an ongoing basis, so please submit your application as soon as possible. Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment. We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.

At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby. About the role We are now looking for a Process Engineer. This team will consist of different competencies, such as biomedicine, biotechnique, validation, automation and mechatronic. You will be responsible for automation/mechatronic knowledge within the department. You will also be responsible for one of our manufacturing processes and drive the work with continues improvements. Whenever there is a question regarding automation/mechatronic from your colleagues you will be asked to help. This is a team with a lot of cross-functional collaborations and responsibilities with both internal and external stakeholders from a variety of countries. Key Responsibilities * Developing and implementing new production processes * Driving continuous improvements on existing processes in close collaboration with all production departments * Ensuring that existing production is compliant for all our in-house production within the business area Process engineering will also work with our outsourced products and the assessment and approval of our suppliers’ processes in close collaboration with our Quality Assurance, Supply Chain and Product Development department. This is a permanent, full-time position based at our office in Gothenburg. Travel and work from other Vitrolife sites and contract manufacturers might be part of the position. Your Profile * Bachelor or master’s degree in biomedicine, chemistry, biology, mechanic, automation or equivalent * Experiences from working with quality standards and processes (ISO-13485, GMP) * 5 years’ experience of automation/mechatronic work * Fluent in Swedish and good knowledge in English both oral and written You are thorough, structured, can see the whole picture and are able to prioritize and meet deadlines. You are also service-oriented, solution-focused and communicative and you enjoy working in a changing and dynamic environment. Applications will be reviewed on an ongoing basis, so please submit your application as soon as possible. Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment. We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.

We are seeking an ambitious applied researcher who wants to work at the forefront of data-driven nutrition and health. This is a unique opportunity to bridge mathematics, statistics, AI, and biomedical research in a highly interdisciplinary research environment. About us Fraunhofer-Chalmers Centre (FCC) is a leading research centre in industrial mathematics, modelling, simulation, optimisation, and data analytics. We operate at the interface between academic research and industrial needs, often in interdisciplinary projects where mathematics, data, and domain expertise meet. Together with the nutrition research group led by Professor Rikard Landberg at Chalmers University of Technology, we conduct advanced research in data-driven nutrition, health, and food science. With large-scale diet and health data, omics data, biomarkers, digital food and health services, we establish predictive models for evaluation of the role of diet in health and disease and establish personalized dietary strategies for more effective disease prevention. In many cases, the work involves time series data, dynamic processes and phenomena, where both methods and interpretation must account for temporal dynamics. Data typically comes from intervention studies conducted in Gothenburg and or from large cohorts and biobanks from international collaborators. To secure and further develop this important collaboration, we are now recruiting an applied researcher with a strong quantitative profile and interest in nutrition, health, or medicine. Your role As an applied researcher in this area, you will: Act as a key person in the collaboration between FCC and the nutrition research group at Chalmers. Lead and conduct research projects in data-driven nutrition, such as:analysis of time series data and dynamic processes, where signals and responses evolve over time. statistical modelling, AI, and machine learning on large epidemiological cohorts, diet and health data analysis of omics data (metabolomics, proteomics, microbiome, etc.) development of predictive dynamical models and digital decision-support tools for nutrition and health method development in causal inference, integration of heterogeneous data sources, uncertainty quantification Work with a wide range of data types, for example dietary records, biomarkers, omics data, registry data, and sensor data such as CGM measurements (continuous glucose monitoring), activity trackers, and other wearable sensors. Serve as a bridge between domain researchers (nutrition, medicine, food science) and quantitative experts (mathematics, statistics, AI&ML, systems engineering). Supervise, collaborate, and support PhD students and postdocs involved in joint projects. Your profile We are looking for someone who: Holds a PhD in Applied Mathematics, Mathematical Statistics, Automatic Control, Signal Processing, Systems Engineering, Data Science, or a related field. Has experience in data-driven research, preferably related to biomedicine, nutrition, epidemiology, food science, or public health. Is proficient in modern statistical modelling, AI & machine learning methods (e.g. system identification, regression models, mixed-effects modeling, Bayesian methods, deep learning, variational autoencoders, generative AI). Is an experienced programmer in R and/or Python, and used to working with large datasets and reproducible analysis workflows. Enjoys working in interdisciplinary environments and is curious about understanding biological/nutritional research questions in depth. It is meritorious if you also: Have experience working with cohort data, registry data, clinical studies, or omics data. Have previously worked in projects involving both academic and industrial/external partners. Have experience supervising PhD students, postdocs, or junior researchers. Can communicate in both Swedish and English; excellent English is required. What we offer With us, you will: Have a unique opportunity to combine advanced quantitative and data-driven methods with cutting-edge research in biomedicine, nutrition, and health. Work in a strong and long-term collaboration between Fraunhofer-Chalmers Centre and Chalmers division of Food and Nutrition Science, with access to both international academic and industrial networks. Influence the direction of a strategically important initiative in data-driven nutrition and health. Be part of a creative, collaborative, and international research environment with good opportunities for personal and scientific development. Employer: Fraunhofer-Chalmers Research Centre for Industrial Mathematics (Fraunhofer-Chalmers Centre, FCC)   Employment: according to agreement   Location: Gothenburg, Sweden   Department: Systems and Data Analysis (in close collaboration with Chalmers)   Application procedure The application should be written in English and attached as PDF-files, containing as specified below. Maximum size for each file is 40 MB. Please note that the system does not support Zip files.  - CV  - Publication list - Transcript of grades - Personal letter with: A brief description of your research profile and how it relates to nutrition/health A brief motivation as to why you are interested in this position.  Please apply no later than 16th August 2026. Evaluation of applications will be done on a continuous basis. Please note: The applicant is responsible for ensuring that the application is complete. Incomplete applications and applications sent by email will not be considered. Contact details to references will be requested after the interview.  For questions, please contact:   Mats Jirstrand, Head of Department, Systems and Data Analysis, Fraunhofer-Chalmers Centre E-mail: mats.jirstrand@fcc.chalmers.se Phone: +46 730 794303

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.