Sökresultat för "Clinical Chemistry"

Akademiska laboratoriet Vi är Akademiska sjukhuset – ett av Sveriges ledande universitetssjukhus. Som länssjukhus och leverantör av högspecialiserad vård erbjuder vi vård till två miljoner människor i Mellansverige. Här händer det ständigt något – ett nytt liv föds, en mormor opereras, en kollega hyllas som hjälte. Hos oss får du uppleva både hårda prövningar och fantastiska händelser, i en stark gemenskap med kollegor. Välkommen med din ansökan! Vår verksamhet Klinisk kemi och farmakologi (KKF) ingår i verksamhetsområdet Akademiska laboratoriet. Vi bedriver högspecialiserad diagnostik dygnet runt och erbjuder kvalificerad vägledning inom kemi och farmakologi. Verksamheten hanterar cirka 6 500 provrör per vardag. Våra analyser är snabba, kvalitetssäkrade och utformade för att stödja hälso- och sjukvårdens processer samt främja forskning och utveckling. Vi tillhandahåller även stöd till patientnära verksamhet inom såväl sluten som öppen vård, liksom provtagning under kontorstid på Akademiska sjukhuset och vid laboratoriet på Lasarettet i Enköping. Inom KKF arbetar cirka 140 medarbetare, och vi strävar efter att vara en attraktiv arbetsplats präglad av professionalism, engagemang och gott ledarskap. Ditt uppdrag Som biomedicinsk analytiker vid Klinisk kemi och farmakologi erbjuds du ett kvalificerat och varierat arbete i en högteknologisk laboratoriemiljö. Arbetsuppgifterna omfattar självständigt laborativt arbete, inklusive preanalytiskt arbete, bedömning och tekniskt godkännande av analyser. Du kommer att ha en huvudsaklig inriktning mot ett av våra laboratorier för specialanalyser och kommer primärt att arbeta med cell och molekylärbiologiska metoder, genotypningar samt flödescytometri. Rollen innebär även ansvar för att bidra till diagnostik, utbildning, information och kvalitetssäkring inom verksamheten. Dina kvalifikationer Vi söker dig som är legitimerad biomedicinsk analytiker. Det är meriterande om du har erfarenhet av liknande arbetsuppgifter från andra sjukhuslaboratorium. Vidare är det meriterande med kunskaper inom provmottagning, allmänkemi, hematologi och koagulation. Du är kvalitetmedveten, arbetar strukturerat och noggrant samt har god samarbetsförmåga, ett ödmjukt förhållningssätt och delar gärna med dig av dina kunskaper. Du är flexibel, lösningsorienterad och trivs i en verksamhet med varierande arbetstempo. Arbetet ställer krav på att du snabbt kan sätta dig in i nya arbetsmoment och kan arbeta både självständigt och i grupp. Goda kunskaper i svenska i tal och skrift är ett krav för tjänsten då arbetet innefattar kommunikation, dokumentation och kvalitetssäkring på svenska. Personlig lämplighet, initiativförmåga och förmåga att snabbt komma in i arbetet kommer att tillmätas stor betydelse. Vi erbjuder Tillsvidareanställning 100%, på Klinisk kemi och farmakologi, Akademiska sjukhuset. Tillträde enligt överenskommelse. Provanställning kan komma att tillämpas. Hos oss får du förmåner som gör skillnad, läs om förmånerna här (https://regionuppsala.se/formaner/). Efter genomförd upplärning ingår tjänstgöring på dagtid (måndag – fredag, 8:00-16:45). När du kommit in i arbetet finns möjlighet att arbeta jourtid (kvällar och helger). Vid regelbundet arbete på obekväm arbetstid utgår ett fast lönepåslag samt ersättning per obekvämt arbetspass, utöver ordinarie OB- och övertidsersättning. Varmt välkommen med din ansökan! För att din ansökan ska vara komplett ska den innehålla: • Ett CV och personligt brev på svenska • Yrkeslegitimation och ev. övriga bilagor Anställningsintervjuer genomförs löpande även under ansökningsperioden. Välkommen med din ansökan snarast. Vill du veta mer? Avdelningschef Hodan Farah hodan.farah@akademiska.se Avdelningschef Mandana Rostampour mandana.rostampour@akademiska.se Facklig kontaktperson (Naturvetarna eller Vårdförbundet) nås via växeln 018-611 00 00 Vill du jobba med oss? Välkommen med din ansökan via länken nedan. Läs om anställningsvillkor och lönesättning inom Region Uppsala här: Bli vår nya kollega (https://regionuppsala.se/jobb-och-utbildning/bli-var-nya-kollega/) Region Uppsala värdesätter de kvaliteter som jämn könsfördelning och mångfald tillför verksamheten och ser gärna sökande av alla kön och med olika födelsebakgrund, funktionalitet och livserfarenhet. Region Uppsala krigsplacerar all tillsvidareanställd personal utifrån totalförsvarets behov. Detta innebär för den enskilda medarbetaren inga förpliktelser i fredstid utan är enkom en planeringsåtgärd. Inför beslut om anställning, sker kontroll av misstanke- och belastningsregister avseende samtliga arbetssökanden som i den sökta anställningen kan komma att arbeta inom psykiatrisk sjukvård, habilitering, vård av barn och ungdom eller tvångsvård av missbrukare, områden som omfattas av fakultativa registerutdrag. Detta gäller således alla som kommer att arbeta patientnära, även om arbetsuppgifterna i nuläget inte är tänkta att huvudsakligen innehålla arbete med ovan nämnda patientgrupper. Denna rekrytering sker helt genom Region Uppsalas försorg och vi undanber oss telefonsamtal från rekryteringsföretag och annonsförsäljare.

Gnothis AB is seeking for a skilled Software Engineer who enjoys building experimental systems in a laboratory environment. This is a permanent position based at our HQ, located at the campus of Stockholm University (Stockholm, Sweden). Gnothis, founded in 2015 and supported by highly innovative industrial professionals and technology developers, is on a mission to develop a new frontier for single molecule DNA sequencing; to break the mold on how sequencing is used as a clinical tool for the diagnosis of complex diseases. Gnothis technology integrates a wide range of cutting-edge sciences ranging from nanotechnology, photophysics, optics, surface chemistry, biochemistry and computational science. Our instrumentation, software and analysis team currently consists of four engineers and we are now expanding the team as we scale development of the system. We are seeking for an engineer with strong data analysis and scientific programming experience to develop our DNA sequencing data analysis pipeline. The role combines algorithm development, image analysis, and scientific data exploration, working closely with our instrumentation and biochemistry teams. The work involves analyzing experimental data from our microscopy-based sequencing platform and developing the automated analysis pipeline that converts raw microscopy data into DNA sequencing results. The position is part of a multidisciplinary team developing a prototype DNA sequencing instrument combining microscopy, microfluidics, nanofabrication and advanced data analysis. Initial Project The initial assignment will be to continuously analyze the latest experimental data from the lab in close collaboration with the biochemistry and instrument teams. This means developing new analysis algorithms, critically reviewing results together with the team, and driving experiment design to better address the research questions. The work includes analyzing fluorescence microscopy data, developing algorithms for tasks such as peak detection and classification, and translating manual analysis workflows into automated pipelines using Python and Airflow. We are seeking for the right candidate who can make confident decisions based on previous experiences connected to laboratory environments (eg. development of diagnostic software tools and/or processing of fluorescence microscopy raw data). Responsibilities Develop algorithms and analysis methods for microscopy-based sequencing data Implement automated analysis pipelines in Python and Airflow Perform exploratory analysis of experimental datasets and extract meaningful insights Collaborate closely with instrumentation and biochemistry teams to interpret results and improve experiments Develop tools for data visualization, evaluation and reporting Contribute to building a robust and scalable DNA sequencing analysis workflow. Candidate Profile For you to enjoy performing expected activities, and being a valuable member in an ambitious and innovative team; we think you are an engineer or scientist with strong experience in scientific programming and data analysis. This role suits someone who enjoys working deeply with experimental datasets and extracting insight through algorithm development, statistical analysis and careful data interpretation. The candidate should be comfortable working independently with complex datasets and driving the development of analysis methods in collaboration with a small multidisciplinary team. Relevant backgrounds and skills include: Master of Science and/or Ph.D educational background – ideally combined with a relevant Life Science focus. Python programming for scientific computing Image analysis and signal processing Microscopy or fluorescence imaging data Statistics and experimental data analysis Scientific visualization and reporting DNA sequencing or genomics data A PhD with strong experience in microscopy data, sequencing data, or similar experimental datasets is highly preferred. Gnothis offer a creative environment focused on technology and product development, a competitive compensation package and plenty of room for self-development as the company expands. This is a permanent position (not consultant assignment). If above sounds like an exciting opportunity and you would like to hear more, do not hesitate and submit your application and we will get back to you! Gnothis AB on LinkedIn: https://www.linkedin.com/company/gnothis/posts/?feedView=all For inquires please email us at: markus.dahl@valleyrecruitment.se

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

Nanexa is now recruiting a Quality Assurance (QA) Manager. The position is full-time and based at our headquarters in Uppsala, and we are looking for a new colleague to join our growing organisation. As a QA Manager at Nanexa, you will play a key role in building and shaping the quality function in a growing pharmaceutical company. This is not a traditional QA role in a large organisation – instead, you will be part of a small, highly skilled team where your contributions will have a direct and visible impact on how we work and grow. You will have the opportunity to develop, implement and continuously improve our Quality Management System while being actively involved in the full product lifecycle – from early development to manufacturing of clinical trial material. The role combines strategic responsibility with hands-on work and close collaboration across functions. At Nanexa, you will not work in a silo. You will be involved across the organisation, working closely with colleagues in development, production and analytics, gaining a broad understanding of our technology, products and processes. As a company of approximately 15 employees, we offer an environment where each individual plays an important role, and where you will actively contribute to building something new. Responsibilities The QA Manager will have a central role in the oversight of manufacturing and analytical activities from a quality perspective, covering the entire chain from development to clinical supply. You will report directly to the Head of Quality Assurance and be an important contributor to the continued development of the QA function and the company as a whole. Your responsibilities will include: - Develop, implement and continuously improve the Quality Management System in line with company growth and regulatory requirements - Assess and approve batch-related documentation such as specifications, batch records, deviations and change requests - Ensure that production and testing of clinical trial materials are conducted in accordance with applicable GMP requirements - Review and approve SOPs, manage periodic reviews and support supplier qualification and re-evaluation - Lead and participate in internal audits and audits of external service providers - Represent QA in cross-functional project teams and contribute to project execution - Provide guidance and support to the organisation in quality-related matters - Perform internal training within GMP and quality systems - Contribute to the strategic development of the QA function and quality processes Your Profile We are looking for a driven and quality-minded professional who enjoys working in a dynamic and developing environment. Key qualifications include: - MSc in Pharmacy, Biology, Chemistry, Engineering, or a related field - Several years of experience within QA in a GMP-regulated pharmaceutical or biotech environment - Experience in development and/or validation of manufacturing or analytical processes - Experience in authoring and reviewing GxP-critical documentation, including SOPs, deviations, CAPAs and change controls - Strong knowledge of Quality Systems and applicable GMP regulations - Fluency in Swedish and English As a person, you are proactive, structured and solution-oriented, with a strong sense of ownership and accountability. You thrive in a dynamic organisation where processes are still being developed, and where you have the opportunity to make a real impact. You are comfortable taking on multiple responsibilities and enjoy working both independently and in close collaboration with others. At Nanexa, each employee contributes to the overall success of the company and you will have the opportunity to influence not only your own area of responsibility, but also the development of the company as a whole. About Nanexa AB Nanexa is a Swedish pharmaceutical company developing long-acting injectable drugs based on our proprietary PharmaShell® technology. We operate at the intersection of material science and drug development, taking projects from early idea through development to proof-of-concept in clinical trials. In addition to our own pipeline, we collaborate with leading pharmaceutical companies to develop new products based on our technology. To learn more about Nanexa, please visit www.nanexa.com For more information about the position, please contact: Krishan Johansson Haque, PhD Sr Recruitment Consultant, QRIOS Life Science & Engineering T: +46 (0)72-070 16 53 E: krishan.johansson-haque@qrios.se

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger. About the Role You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements. Key Responsibilities Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes. Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance. Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices. Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes. Design and evaluate smoke studies to verify airflow performance and first-air protection. Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies. The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week. Your Profile You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind. Qualifications Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment. Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations. Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing. Proven track record leading deviation investigations, root cause analyses, and CAPA implementation. Excellent analytical, problem-solving, and technical writing skills. Strong stakeholder management and collaboration across multiple functions. Ability to independently manage complex projects and drive continuous improvement initiatives. Application If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application. About Galderma Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ, the skin, meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to over 800 professionals working across R&D, manufacturing, clinical development, and commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

Drive innovation where it matters Make your next move matter At Mölnlycke, we believe that real impact starts with people. People who are bold enough to challenge the status quo. People who care deeply about their work, their colleagues, and the world around them. People who know exactly why they do what they do. As a global medical solutions company, we design and deliver innovative products and services across wound care, operating room solutions, gloves, and antiseptics. Our mission is to advance performance in healthcare by supporting professionals, improving outcomes, and making a difference where it matters most. In Wound Care, we help to prevent, manage and accelerate the healing of wounds. Where you’ll make a difference Mölnlycke is now looking for a Packaging Developer to join our R&D Wound Care Packaging & Artwork team at our headquarters. In this role, you’ll contribute to meaningful work that improves lives. You will collaborate across teams, bring your ideas to the table, and help shape innovative packaging solutions that support both patients and healthcare professionals. Here’s how you’ll make an impact: Drive and execute packaging change projects with defined scope and impact Develop and implement new or improved packaging solutions to meet customer needs and regulatory requirements Own technical documentation and ensure compliance with global standards for medical device packaging Collaborate with procurement and suppliers, leading technical discussions, support audits, and build partnerships Identify and propose new packaging technologies, materials, and suppliers Act as a key contributor in cross-functional teams including R&D, project management, and process development Support sustainability initiatives through development of smarter, more sustainable packaging solutions What you’ll get Be part of a culture built on trust, care, and shared ownership. Your growth and development Opportunities to expand your expertise in packaging and medical device development Exposure to cross-functional collaboration and strategic decision-making Potential career paths into senior development roles, project management, or leadership Flexibility, wellbeing and benefits A collaborative, supportive, and highly experienced team environment Opportunities to make a real difference for customers, patients, and the environment Competitive compensation and benefits package A workplace that values wellbeing, inclusion, and continuous improvement What you bring We’re looking for someone who combines technical expertise with curiosity and a collaborative mindset. Must-haves Bachelor’s or Master’s degree in engineering, chemistry, life sciences, or equivalent Around 5 years’ experience in product/material development from medical devices, or packaging development from other regulated industry Fluent English, written and spoken Strong communication and stakeholder collaboration skills Key strengths and mindset High level of accuracy and attention to detail A collaborative, positive, and solution-oriented approach Curiosity and a genuine interest in sustainable packaging innovation and development Ability to balance technical rigor with business needs Nice to have Experience working with packaging materials such as paper, plastics, or bottles Interest or experience in sustainable packaging solutions Strong knowledge of design control and regulated environments Understanding of global regulatory requirements for packaging Please submit your application by August 9th. As we approach the holiday season, interviews are planned to take place in August. Our approach to Diversity & Inclusion We’re building a workplace where everyone feels seen, heard, and valued. We believe that a diverse mix of people makes us stronger—bringing fresh perspectives, driving better decisions, and helping us deliver solutions that reflect the world we serve. Inclusion isn’t just a value—it’s how we work, grow, and lead together. About Mölnlycke Mölnlycke is a world-leading medical products and solutions company that equips healthcare professionals to achieve the best patient, clinical and economic outcomes. Our business is organised in four business areas: Wound Care, Operating Room Solutions, Gloves and Antiseptics, with customer centricity, sustainability and digitalisation at the heart of everything we do. We employ around 8,700 people globally, with headquarters in Gothenburg, Sweden, and operations in more than 100 countries. Mölnlycke is a founding partner of GoCo Health Innovation City and has been part of Investor AB since 2007.

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.