Galderma is global leader in dermatology, present in 90 countries with a science-driven portfolio spanning Aesthetics, Skincare, and Therapeutics. Since 1981, we’ve been dedicated to advancing dermatology and delivering meaningful outcomes for consumers, patients, and healthcare professionals. Galderma’s Uppsala site is rapidly expanding! A new manufacturing facility is near completion, and we are growing our team to meet increasing demand of our medicinal products. We seek driven, collaborative individuals who embrace learning and bring positive energy. At Galderma, you’ll find an inclusive culture that empowers personal growth while making a real impact. Join us in shaping the future of dermatology! We are now looking for a eager person to contribute as Senior Manufacturing Scientists in our department focused on Assembly & Packaging.. About the roleThe roles act as subject matter expert (SME) responsible for new product implementation (NPI) into a manufacturing facility, and for set up and support in productions processes injector assembly, visual inspection and packaging. You will be part of a team and collaborate with cross-functional teams, including production, quality assurance, regulatory affairs, and process development, to ensure thorough investigation and perform risk assessments. Key responsibilities: Develop NPI strategy and support all aspects of process validation, including writing process validation documentation, executing process validation, performing process data reviews, investigations, risk management, and change implementation. Serve as SME representing MS&T in Technology Transfer projects. Lead and participate in investigations of deviations, incidents, and anomalies within the manufacturing process.  Provide SME assessments in investigations and change controls as required. Prepare detailed investigation reports, conveying findings and recommendations to management and relevant stakeholders. Maintain comprehensive records of investigations, findings, actions taken, and recommendations, ensuring compliance with regulatory and quality standards Write technical manufacturing documentation and dossier sections and provide responses to regulatory authorities as needed. The positions are permanent with a 6-month probation period, based in Uppsala, and the employment contract will be directly with Galderma. Your ProfileTo succeed in this role, you need a BSc or MSc in a relevant scientific or engineering field and solid experience from relevant work. We work in a fast-paced environment where proactivity and taking responsibility is of essence. Skills & Qualifications Bachelor’s or master’s degree in a relevant scientific or engineering field Approximately 6 years of experience in a biopharmaceutical or medical device.  Knowledge of regulatory requirements related to investigations and cGMP Strong knowledge of investigative methodologies and root cause analysis techniques. Experience from either process validation for manufacturing steps such as injector assembly, visual inspection and packaging. Proficient in English, with Swedish as a plus. About Galderma Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee. Application If you believe this could be the right career move for you, please send in an application as soon as possible. We evaluate applications continuously, so don’t wait to apply. If you have any questions, please don’t hesitate to reach out to Sandra Bydell Sveder, Partner & Senior Recruitment Consultant at SallyQ.

At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world.We are in the process of ramping up production at our new state-of-the-art manufacturing facility in Uppsala. To follow through with this expansion we need ambitious, forward driven and skilled leaders with the ability to create self going teams of specialists who thrive and prosper in a fast paced and growth environment that demand top level of operational excellence. The role:We are now recruiting a Manager Device Injectables to join our Manufacture, Science and Technology (MS&T) department. As Manager Device Injectables, you will lead and coordinate the development, industrialization, and continuous improvement of our injectable medical devices. You’ll also have the exciting opportunity to build and manage a team of manufacturing scientists focused on new product implementation (NPI) for our new state-of-the-art manufacturing facility, while supporting commercial manufacturing activities. You and your team are responsible for: Implementing plans and programs, support policies and practices enabling new product manufacturing, end-to-end. Enabling smooth transition of products from R&D into full production readiness, with team members representing MS&T in Technology Transfer projects and taking full process ownership Ensuring process efficiency, cycle time, reliability, and serviceability. Process validation (PV), process trending programs, and continuous process verification (CPV) where applicable. Ownership for medical device design control documentation following product design transfer You’ll work with individuals who share your passion, as well as those who bring different perspectives—because we believe diversity drives innovation. We value each team member's unique strengths and foster a culture of professionalism, collaboration, and support. It’s the kind of environment where people thrive and achieve their best. As a manager, you will play a key role in promoting teamwork and partnership, both within the organization and with external stakeholders, to deliver integrated and effective solutions. The position is a permanent with 6 months of probation period,  based in Uppsala and the employment contract will be directly with Galderma.  The Profile We believe you have solid experience from relevant work in a regulated industry, preferably from the biopharmaceutical or medical device industry, with experience in sterilization. We also hope that you have experience from implementing manufacturing and leading a team. You thrive in a dynamic work environment with extensive cross functional contact both internally and external.  Skills & Qualifications: BSc or MSc degree in a relevant scientific or engineering field, such as Chemistry, Biochemistry, Chemical Engineering, or solid experience of working in a regulated industrial environment. Approximately 8 years of experience with either in a biopharmaceutical and/or medical device environment. Previous team management experience. Hands on experience with manufacturing processes, control strategies and product interactions within either Experience in processes regarding either Filling or /and Sterilization. Fluent in English Swedish is highly meritourous. About GaldermaGalderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee. ApplicationIf 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. If you have any questions please do not hesitate reaching out to Ellinor Crafoord, CEO & Senior Recruitment Consultant at SallyQ.

At Galderma, we inspire our teams with a shared belief in our bold ambition to become the world’s leading dermatology company. As we expand operations at our state-of-the-art manufacturing facility in Uppsala, we’re looking for driven, visionary leaders to join us. To support this growth, we need skilled leaders who can build high-performing teams of specialists—teams that excel in a fast-paced environment where operational excellence is key. The Role  We are now recruiting a Manager Assembly and Packaging to our Manufacture, Science and Technology (MS&T) department. You will be responsible for overseeing the day-to-day operations of our assembly and packaging lines, ensuring all processes are executed safely, efficiently, and in compliance with quality standards. This role involves managing a cross-functional team, driving continuous improvement initiatives, and supporting the launch of new products. You’ll have the opportunity to build and lead a team of manufacturing scientists focused on new product implementation (NPI) in our new facility, while supporting ongoing commercial operations. You and your team are responsible for: Implementing plans and programs, support policies and practices enabling new product manufacturing, end-to-end. Enabling smooth transition of products from R&D into full production readiness, with team members representing MS&T in Technology Transfer projects and taking full process ownership Process validation (PV), process trending programs, and continuous process verification (CPV) where applicable. Ownership for medical device design control documentation following product design transfer You’ll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do. As a manager you will be an ambassador in fostering cooperation and partnership internally and externally to provide integrated solutions to problems.  The position is a permanent with 6 months of probation period,  based in Uppsala and the employment contract will be directly with Galderma.  The Profile We believe you have solid experience from relevant work in a regulated industry, preferably from the biopharmaceutical or medical device industry, with experience in sterilization. We also hope that you have experience from implementing manufacturing and leading a team. You thrive in a dynamic work environment with extensive cross functional contact both internally and external.  Skills & Qualifications: BSc or MSc degree in a relevant scientific or engineering field, such as Chemistry, Biochemistry, Chemical Engineering, or solid experience of working in a regulated industrial environment. Approximately 8 years of experience with either in a biopharmaceutical and/or medical device environment. Previous team management experience. Hands on experience with manufacturing processes, control strategies and product interactions within either Experience in processes regarding injector assembly and/ or packaging processes. Fluent in English About GaldermaGalderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee. ApplicationIf 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. If you have any questions please do not hesitate reaching out to Ellinor Crafoord, CEO & Senior Recruitment Consultant at SallyQ.

Cavidis mission är att göra pålitlig diagnostik tillgänglig och de har bland annat utvecklad Exazym teknologin som möjliggör en kraftfull signalförstärkning för immunoassays. Det finns nu ett tydligt fokus på produktlansering och ökad försäljning. Bolaget består av ett mindre team dedikerade kollegor som nu är i behov av dig som Director of Operation. Om rollen Som Director of Operation har du en central roll där du leder ett engagerat team med ansvar för produktion och utveckling, säkerställer effektiva arbetsprocesser och driver vårt dagliga arbete framåt. Rollen är bred och du kommer att jobba nära VD och i samarbete med alla bolagets funktioner. Du är oljan i maskineriet som säkerställer balansen mellan struktur, effektivt och kreativitet. Dina huvudsakliga arbetsuppgifter: Produktionsplanering, idag i Excel – men vi ser gärna att du utvecklar och föreslår förbättrade arbetsprocesser och/eller systemstöd. Ansvar för batchprotokoll – skriva, granska, kvalitetssäkra. Operativ personalledning – du har fem direktrapporterande med ansvar för produktion och utveckling. Deltagande i projektmöten – fördela arbete, driva framsteg, agera länken mellan funktioner. Uppföljning av produktionskostnader – för balans- och likviditetsprognoser. Leverantörsförhandlingar – från behov till beställning. Kemikalieansvar – inklusive kontakt med myndigheter och ansvar för kemikalielagret. Din profil Du gillar struktur och tydlighet, men trivs också i ett sammanhang där saker inte alltid är helt på plats – än. Du leder genom närvaro och tillit, med ett coachande förhållningssätt.  Vi söker någon som har: Universitetsexamen som ingenjör eller naturvetenskap med fokus på molekylärbiologi, kemi eller motsvarande. Erfarenhet av ledarskap från tidigare chefsroll, teamledning och/eller projektledning. Förståelse och erfarenhet av kvalitetsreglerad laborativ produktion och eller utveckling, gärna från bolag med liknande verksamhet.  Erfarenhet av att utveckla och leda operativa processer.  Kunskaper i svenska och engelska, både i tal och skrift.  Vi misstänker att du antingen är i början eller mitten av din ledarskapskarriär, har rätt grundkompetens och vill växa in i rollen eller har lång erfarenhet och söker en något mindre intensiv roll på 80–100%.  Vi söker inte någon på jakt efter nästa VD-steg – här är din styrka att vara stabil, engagerad och närvarande. Om Cavidi Vi är ett litet och passionerat bolag med baserade i Uppsala. Vår mission är att förbättra tillgången till avancerad diagnostik – globalt. Just nu står vi inför flera spännande produktlanseringar, nya distributörer i USA och Europa samt ökat kommersiellt fokus. Vi har egna labb i Uppsala Business park där produktionen sker, den är inte komplex men en viktig och noggrann process. Arbetsmiljön präglas av gemenskap, tydlighet och glädje – konflikter är sällsynta, och vi gillar att ha roligt tillsammans. Arbetet utförs till stor del på plats i våra lokaler.  Intresserad? Är du nyfiken – skicka in din ansökan! I den här rekryteringen samarbetar vi med SallyQ, så alla initiala frågor hanteras av Sandra Bydell Sveder, Senior Rekryteringskonsult. Tveka inte att höra av dig till henne med eventuella frågor (E: [email protected] eller M: 0763199688).

We are currently looking for a Scientist or Senior Scientist to join our expanding team of passionate professionals focused on delivering impactful results for our partners. The company is a pioneering life science company committed to accelerating drug discovery through innovative technologies and expert scientific collaboration. This is an exciting opportunity for a driven individual with a strong background in Biochemistry, Biophysics, Cell Biology, or a related field to contribute to a growing company where science, curiosity, and collaboration are at the core of everything we do. Key responsibilities: Leading and managing scientific projects from design through delivery. Supervising and mentoring junior team members. Driving multiple projects simultaneously in a dynamic, customer-focused environment. Conducting extensive hands-on lab work with a focus on quality and precision. Ensuring high standards in documentation, reporting, and protocol adherence. Communicating scientific results clearly and confidently to customers (written and verbal). Qualifications: Master’s or PhD in Biochemistry, Biophysics, Cell Biology or a related field. Minimum 2 years of relevant industry or research experience. Proven experience in project leadership and cross-functional teamwork. Preferred experience and skills: Practical knowledge of LC-MS workflows and instrumentation. Hands-on experience with MS sample preparation (especially peptide-based workflows). Familiarity with proteomics data analysis, including interpretation and visualization of complex datasets. You'll be part of a dedicated team pushing the boundaries of what’s possible in drug discovery. We value scientific excellence, curiosity, and the ability to turn complex data into meaningful insights. This is a fixed-term employment of 12 months where you will be employed by the customer. Apply already today, as selection and interviews take place on an ongoing basis. Welcome with your application!

This company is a life science company that is dedicated to advancing drug discovery through innovative technologies. As part of their continued growth, we are seeking a highly motivated and detail-oriented Mass Spectrometry Research Associate for a consultant assignment. Some key Responsibilities: Perform routine and project-based mass spectrometry workflows in a core facility or analytical setting. Operate and maintain HPLC and LC-MS instrumentation, including troubleshooting and system optimization. Execute general laboratory tasks, including pipetting and standard reagent preparation. Ensure accurate data acquisition, processing, and transfer of mass spectrometry data. Maintain adherence to established laboratory protocols, documentation standards, and safety regulations. Qualifications: Relevant academic background in analytical chemistry, biochemistry, biotechnology, or a related field. Demonstrated experience working in a core facility or routine analysis environment. Strong practical knowledge of HPLC/LC-MS systems, with the ability to perform routine maintenance and troubleshooting. Proficiency in standard laboratory techniques and good laboratory practices (GLP). Experience with mass spectrometry data handling, including software for acquisition and processing. Strong attention to detail, organizational skills, and a commitment to high-quality work. Excellent written and verbal communication skills in English. We offer a collaborative and supportive environment where scientific integrity and innovation are highly valued. We provide opportunities for professional growth while contributing to impactful science at the forefront of drug discovery. This is a 4-month consultant assignment, during May to August. Apply already today, as selection and interviews take place on an ongoing basis. Welcome with your application!

Scandinavian Biopharma är ett forskningsbaserat biotechföretag fast beslutna att hjälpa människor i hela världen till ett bättre och längre liv. De är på god väg att göra så genom utveckling av världens första vaccin mot ETEC-bakterier. ETEC infektioner kan bli svåra hos både barn och vuxna med svåra diaréer som följd. Mest utsatta är små barn som kan få bestående men och även avlida till följd av infektionen. Scandinavian Biopharma distribuerar även i främst norra Europa, ett brett sortiment av biologiska specialistläkemedel med fokus på vacciner och immunglobuliner. I dagsläget har SB redan lovande säkerhets och skyddsdata för ETVAX från fas 2b-studien hos finska resenärer till Benin, Västafrika. Vi har vaccinerat 5 000 barn i en fas 2b-studie i Gambia och förbereder som bäst inför en effektstudie (fas 3) studie i USA och en stor effektstudie i Zambia (fas 3). SB är välfinansierade både av internationella statliga medel samt genom SBs egna distributionsverksamhet. Downstream Process Development ScientistCMC gruppen på Scandinavian Biopharma består av 15 kollegor. Gruppen utökar sin inriktning mot processutveckling, allt eftersom de närmar sig kommersialisering av sitt vaccin mot ETEC. Därför söker nu Scandinavian Biopharma en nyfiken och lösningsorienterad Downstream Process Development. Scientist för arbete med processutveckling för våra 6 DS komponenter. Arbetet innefattar både att utveckla robusta processer, formuleringsutveckling och Tech transfer. I rollen arbetar du både laborativt och administrativt och du samarbetar mycket med övriga kollegor inom gruppen och inom andra funktioner på företaget samt med externa kontakter. Rollen innefattar bland annat: Arbeta med CMC-utvecklingen av vår vaccinkandidat. Arbeta med processutveckling internt på vårt lab och stödja Tech Transfer till våra CMOer. Delta i framtagande av regulatorisk dokumentation till myndigheter. Utfärda och revidera SOPar. Leda laboratorieutredningar, avvikelseutredningar och initiera CC och CAPA-ärenden. Identifiera effektiviseringsmöjligheter och driva förbättringsarbete. Samarbeta med våra tillverkare. Vem är du? Scandinavian Biopharma söker dig som trivs på ett entreprenörsdrivet bolag och i en roll som blandar utvecklingsarbete, laborativt arbete och rapportskrivande. Du är noggrann, har integritet men är också flexibel. Du är nyfiken, samarbetar gärna tvärfunktionellt och är lösningsorienterad och positiv. Du är duktigt på att tydligt förklara din expertis och gillar att dela kunskap med andra. Din utbildning och erfarenhet: Universitetsutbildning inom mikrobiologi, biokemi, molekylärbiologi eller immunologi. Erfarenhet av CMC-utvecklingsprojekt och Tech transfer. Arbetat laborativt inom läkemedelsindustrin med Downstream processutveckling under minst 3 år. God förmåga att kommunicera i tal och skrift (engelska och svenska). Meriterande erfarenhet: Kunskap inom immunologi. Licentiat eller doktorsexamen. Erfarenhet av oral vaccinutveckling. Möjligheter Scandinavian Biopharma är entreprenörer och experter inom global vaccinutveckling, tillverkning, registrering och kommersialisering av bioläkemedelsprodukter. Vår arbetsmiljö präglas av våra kärnvärden där lagarbete, talang, och personlig utveckling aktivt främjas. Scandinavian Biopharma är världsledande i diarrévacciner mot ETEC. Scandinavian Biopharma består av ett sammansvetsat team med godgemenskap och med en spännande resa framför oss – hoppas du vill vara med oss på denna resa! Tjänsten är en tillsvidareanställning på Etvax AB med placering i Solna, arbete utförs på plats. Rollen rapporterar till VP CMC Development. Ansökan:I denna rekrytering samarbetar Scandinavian Biopharma med SallyQ. Om du är intresserad av tjänsten och vill ha mer information, kontakta Ellinor Crafoord, senior rekryteringskonsult, 079–3554257 eller [email protected]. Ansök via Sallyq.se Sista ansökningsdag: 5 maj 2025, men urval och intervjuer sker löpande så vi välkomnar din ansökan redan idag.

Scandinavian Biopharma är ett forskningsbaserat biotechföretag fast beslutna att hjälpa människor i hela världen till ett bättre och längre liv. De är på god väg att göra så genom utveckling av världens första vaccin mot ETEC-bakterier. ETEC infektioner kan bli svåra hos både barn och vuxna med svåra diarréer som följd. Mest utsatta är små barn som kan få bestående men och även avlida till följd av infektionen. Scandinavian Biopharma distribuerar även i främst norra Europa, ett brett sortiment av biologiska specialistläkemedel med fokus på vacciner och immunglobuliner. I dagsläget har Scandinavian Biopharma redan lovande säkerhets och skyddsdata för ETVAX från fas 2b-studien hos finska resenärer till Benin, Västafrika. Vi har vaccinerat 5 000 barn i en fas 2b-studie i Gambia och förbereder som bäst inför en effektstudie (fas 3) studie i USA och en stor effektstudie i Zambia (fas 3). SB är välfinansierade både av internationella statliga medel samt genom Scandinavian Biopharmas egna distributionsverksamhet. Tjänsten som Drug Substance Specialist Scandinavian Biopharma stärker nu upp teamet inom Manufacturing och söker en engagerad och erfaren Drug Substance Specialist som vill vara med på resan att inom kort ha ett kommersiellt tillgängligt ETEC-vaccin på marknaden. Manufacturing teamet jobbar endast med external Manufacturing och ansvarar för samarbetet med globala CMO nätverk för produktion av företagets läkemedelsprodukter. I rollen som Drug Substance Specialist har du en nyckelfunktion i arbetet med tillverkning och uppskalning av våra 6 Drug Substance komponenter som ingår i vårt ETEC vaccin som är i sen utvecklingsfas. Arbetet inkluderar Technology Transfer av tillverkning till våra kontraktstillverkare (CMO:er), koordinering av processutvecklingsarbete och säkerställa tillverkning av klinikmaterial. Rollen innehåller mycket samarbete externt med CMO:er och även internt med medarbetare inom Manufacturing, Development, Regulatory och QA avdelningarna. Huvudsakliga arbetsuppgifter: Tech Transfer. Processvalidering. Skriva och granska tillverkningsmetoder, valideringsprotokoll och annan produktionsdokumentation. Skriva rapporter för produkt och produktion av bioteknologiska substanser. Skapa goda och långsiktiga relationer med samarbetspartner CMO. Sammanställa och utvärdera resultat från produktion hos CMO. Skriva/granska regulatoriska dokument som ingår i CMC. Tillsammans med teamet på Manufacturing bidra till att produktion av Drug Substance hos CMO sker effektivt och enligt GMP. Stödja processvalidering som är utlagd på CMO, vilket kan innebära resor. Vi söker dig som trivs på ett entreprenörsdrivet bolag och i en roll som blandar praktiskt arbete med mer övergripande strategiska uppgifter. Du är noggrann, har integritet men är också prestigelös i ditt samarbetssätt samt tar ägarskap. Du samarbetar gärna tvärfunktionellt inom organisationen och drivs av att skapa resultat framåt och säkerställa bra processer för extern tillverkning.   Du erbjuds ett ansvarsfullt jobb i ett stimulerande klimat med högt i tak och blir en del av en grupp ambitiösa och duktiga medarbetare som har roligt på jobbet! Utbildning, kvalifikationer och erfarenhet: · Universitetsutbildning inom Civilingenjör bioteknik, farmacevt, Biokemi eller liknande naturvetenskaplig utbildning. · Flerårig erfarenhet av odling och rening inom läkemedelstillverkning. · Erfarenhet av arbete med CMO:er. · Erfarenhet av cGMP tillverkning av biologiska läkemedel och vacciner. · God förmåga att kommunicera i tal och skrift (engelska o svenska). Tjänsten är på heltid och rapporterar till VP Manufacturing, kontoret är placerat i Solna. Ansökan I denna rekrytering samarbetar Scandinavian Biopharma med SallyQ. Om du är intresserad av tjänsten och vill ha mer information, kontakta Ellinor Crafoord, Senior rekryteringskonsult, 079-3554257 eller [email protected]. Sista ansökningsdag: 30 april 2025, men urval och intervjuer sker löpande så vi välkomnar din ansökan redan idag. Om oss Vi är entreprenörer och experter inom global vaccinutveckling, tillverkning, registrering och kommersialisering av bioläkemedelsprodukter. Vår arbetsmiljö präglas av våra kärnvärden där lagarbete, talang, och personlig utveckling aktivt främjas. Vi är världsledande i diarrévacciner mot ETEC. På Scandinavian Biopharma är vi ett sammansvetsat team med god gemenskap och med en spännande resa framför oss – vi hoppas du vill vara med oss på denna resa!

As our Digital Marketing Specialist you will play a vital role in bridging the gap between our innovation and its users. By translating scientific advancements into clear, compelling stories, this role helps ensure that healthcare professionals around the world understand the value and potential of our solutions. Through strategic content, digital campaigns, and a strong online presence we will amplifies our mission—supporting quicker, more accurate diagnostics that can ultimately save lives. Key Responsibilities Develop and execute targeted digital marketing strategies to position QuickMIC in the global diagnostics market. Manage and expand the company’s website (WordPress), ensuring clear and relevant content that supports product applications. Create high-quality content (text, graphics, photo/video) for newsletters, social media, and sales support—aligned with brand and messaging. Lead collaboration with external content agencies and partners (e.g., video production, webinars, campaigns). Translate scientific and technical features into accessible, benefit-driven communication for healthcare audiences. Analyze marketing performance data and market trends to refine messaging and identify new opportunities. Your Profile We’re looking for someone who dares to stand out, since we believe bold creative communication is essential to show the true life-saving potential of our technology. If you are creative and a self-driven individual with strong communication skills and a strategic mindset you will most likely fit in. We are in start-up phase so you should be comfortable managing multiple stakeholders and standing by your ideas with well-formulated arguments. Qualifications & Experience Either a university degree in Life Science and relevant work experience from a similar marketing role or a degree in marketing or communication with work experience from the Life Science industry. Strong skills in content marketing, SEO, Google Analytics, and social media platforms. Excellent written and spoken English (Swedish is a plus). Ability to translate complex scientific concepts into engaging marketing content. Analytical skills to assess market data and optimize strategies. Experience with WordPress and basic graphic design skills are beneficial. What We Offer A dynamic and friendly work environment in a growing company. The opportunity to work with cutting-edge technology that makes a real difference. A collaborative team with a mix of experienced and new talents. You will be part of the sales and marketing team but collaborate cross functional over the whole company. This position is at junior-associate level and this will be an opportunity beeing part of a skilled and dedicated team to learn from.  "Our co-workers are Gradientech’s most valuable resource. We prioritise health and safety and are committed to offering a workplace where employees can develop to their full potential."- Sara Thorslund, CEO and Co-Founder About Gradientech At Gradientech, we are pioneers in the global rapid-AST market, providing an ultra-fast platform for detecting antibiotic resistance through our patented technology. Our flagship product, QuickMIC, is designed to help physicians optimize treatment for critically ill sepsis patients. Our mission is to deliver the best possible diagnostic tools to support healthcare professionals in their life-saving work. Learn more at www.gradientech.se Ready to Make an Impact? If you are excited about innovation and want to contribute to life-saving technology, we would love to hear from you! Gradientech is collaborating with SallyQ for this recruitment and if you have any questions, please do not hesitate to reach out to Sandra Bydell Sveder, Senior Recruitment Consultant (0763199688) We are accepting CVs until 30th of April. We look forward to your application!

Are you a business-driven professional with a passion for sales and the life science industry? Do you thrive in building and deepening business relationships? SwedenBIO, Sweden’s leading industry association for the life science sector, is looking for a Key Account Manager to drive sponsorship sales for our flagship event NLSDays. About the Role As Key Account Manager, your primary focus will be selling and developing sponsorships opportunities for our annual conference, Nordic Life Science Days (NLSDays), a key meeting point for the life science industry in the Nordic region. You will work with an established foundation of existing partners while also identifying new business opportunities. This role requires a proactive and confident salesperson who is not afraid to ask for the deal. Most of the sales will be conducted digitally, meaning traveling is limited. Our clients are big pharma, investors, regions and other companies actively working in the life science industry. You will work closely with our small but dynamic team, ensuring the success of our event and delivering value to our sponsors. The role is preferably based in Stockholm and working from home will be possible upto three days / week when the tasks allow. Your profile We believe you have either: Solid experience in a similar B2B sales role, preferably in sponsorship or event sales in an international setting. OR a background in the life science sector and in the beginning of your career in sales. To succeed in this role, you should be: Business-driven – You understand how to create value for sponsors and partners. Relationship-oriented – You enjoy working with long-term partnerships. Confident & proactive – You have the courage to ask for the deal and close sales. Structured & independent – You take ownership of your work and drive results. Experience and knowledge in life science is beneficial. Your working language will be English, understanding Swedish is a bonus. About NLS Days Nordic Life Science Days (NLSDays) is the largest partnering conference in the Nordics for the global life science industry. The event brings together biotech, pharma, medtech, and digital health companies with investors, decision-makers, and business developers to foster innovation and collaboration. SwedenBIO organizes the event annually, providing a unique opportunity to be at the forefront of industry networking and deal-making. Why Join SwedenBIO? At SwedenBIO, you will be part of a passionate team dedicated to strengthening the Swedish life science sector. This is an opportunity to work in a high-impact role with a broad industry network and significant growth potential. Application Are you ready to take on this exciting challenge? Apply today! In this recruitment SwedenBIO collaborates with SallyQ. If you have any questions, please do not hesitate to contact Sandra Bydell Sveder, Partner & Senior Recruitment Consultant at SallyQ. Please send in your application no later than 30th of Mars. About SwedenBIO SwedenBIO is the national trade association for the life science industry in Sweden. Our member companies develop biotechnology, diagnostics, pharmaceuticals, and medical technology or are experts in areas such as business development, IP, and law. We also bring together investors, incubators, science parks, regional investment promotion organizations, and many more. What unites our members is their instrumental role in developing medical innovations that improve human health in Sweden and globally—whether they are individual entrepreneurs or large multinational life science companies. SwedenBIO is a non-profit membership organization. Its highest decision-making body is the general assembly, which also appoints the organization's board. The day-to-day operations are managed by a team based in central Stockholm.