Research Engineer

SVERIGES LANTBRUKSUNIVERSITET

Department of Soil and Environment About the position The exact tasks will depend on the skillset of the researcher and desired employment duration, but will include anaerobic cultivation of bacteria, single cell RNA sequencing, and communication with collaborators. Your profile The applicant must have expertise in molecular methods and be able to communicate effectively in oral and written English. The applicant is expected to have a lab-based PhD in the biological sciences, though applicants with a masters degree and at least two years of full-time lab experience in molecular biology after completion of their degree will also be considered. Experience in one or more of the following will be seen as assets: single cell RNA sequencing, anaerobic cultivation, bacterial physiology, project management, and method development. Personal fit will be an important part of the evaluation process. Important traits are the ability to work critically and independently, manage time efficiently, show attention to detail, and come to work each day enthusiastic. Due to the short-term nature of this position, candidates already located within commuting distance of Uppsala will be favored. About us The Department of Soil & Environment conducts research, environmental monitoring & assessment and higher education for sustainable soil management in agriculture, forestry and urban environments. Outcomes are aligned to and contribute towards national and international strategies on food security, national environmental objectives and climate reporting as well as the 2030 Agenda for Sustainable Development. The majority of the department's activities and employees are located in the Soil-Water-Environment building on the SLU Ultuna campus in Uppsala, and there is a research group and a field research station situated in Skara. Read more about our benefits and working at SLU by visiting: https://www.slu.se/en/about-slu/work-at-slu/ Location: Uppsala Form of employment: Fixed-term employment 3 months Scope: 80% - 100% Start date: As agreed. Application: Please submit your application before deadline 10th of August 2026. You can submit your application by clicking the button below. Union representatives: https://internt.slu.se/en/my-employment/employee-associations/kontaktpersoner-vid-rekrytering/ The Swedish University of Agricultural Sciences (SLU) has a key role in the development for sustainable life, based on science and education. Through our focus on the interaction between humans, animals and ecosystems and the responsible use of natural resources, we contribute to sustainable societal development and good living conditions on our planet. Our main campuses are located in Alnarp, Umeå and Uppsala, however, the university also operates at research stations, experimental forests and teaching sites throughout Sweden. SLU has around 4,000 employees, 6,000 students and doctoral students and a turnover of over SEK 4,5 billion. We are investing in attractive environments on all of our campuses. We strive to provide a work environment characterised by inclusivity and gender equality, where different experiences generate conversations between people and pave the way for science, creativity and development. Therefore, we welcome applications from people with diverse backgrounds and perspectives.

People Services 4 U Sweden AB

Food Scientist – Food Research Laboratory About PureFize Technologies AB PureFize Technologies AB develops a patented, mercury-free broad-spectrum UV technology that uses optimized UV wavelengths to reduce microbial contamination on food surfaces, water, and materials. In food applications, the technology improves microbiological safety, extends shelf life, and helps preserve product quality while reducing the need for chemical disinfectants. Position Overview We are seeking a highly motivated Food Scientist to join our Food Research Laboratory. The successful candidate will contribute to the development and validation of innovative UV-based food decontamination technologies by planning, executing, analyzing, and reporting laboratory studies focused on food safety, quality, and shelf-life. The position involves research on a wide range of food matrices, including fresh produce, dry seeds, grains, and food-grade powders, with emphasis on microbiological safety, physicochemical quality, and sensory properties. Key Responsibilities Plan and execute laboratory experiments to evaluate the effectiveness of broad-spectrum UV technology on food products. Perform microbiological, physicochemical, and sensory analyses to assess food safety and quality. Optimize and validate treatment conditions for different food materials. Design experiments and perform statistical analyses to interpret research results. Develop technical reports and present experimental findings. Model and evaluate food shelf-life based on microbiological and quality data. Maintain laboratory documentation and ensure compliance with ISO/IEC 17025 quality requirements. Collaborate with multidisciplinary teams in research and product development. Essential Qualifications MSc or PhD in Food Science, Food Technology, Microbiology, or related discipline. Strong experience in planning, executing, and reporting microbiological, physicochemical, and sensory analyses for quality assessment of fresh produce, grains, seeds, and food-grade powders. Experience with experimental design and multivariate statistical analysis. Knowledge of shelf-life studies and predictive modeling. 3-5 years’ experience working in food laboratories operating under ISO/IEC 17025 requirements. Strong scientific writing and data interpretation skills. Excellent organizational and problem-solving abilities. Good written and spoken English. Desirable Qualifications Experience with food preservation or non-thermal processing technologies (UV, light, cold plasma, etc.). Knowledge of food microbiology, HACCP, and food safety regulations. Experience using statistical software such as Minitab, R, JMP, or similar. Ability to work independently while contributing effectively within a multidisciplinary team. Organized, proactive, and detail-oriented with excellent teamwork and communication skills. Interested? This recruitment goes through our consultant Arne Dahlberg. Please apply with your resume to adahlberg@peopleservices4u.com

CTC Clinical Trial Consultants AB

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.