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. External Sourcing LeadI rollen som External Sourcing Lead ansvarar du för att koordinera samarbetet med våra kontraktstillverkare och säkerställa en effektiv End-to-End supply chain – från startmaterial till leverans av kliniskt och kommersiellt material. Du ser till att rätt material finns i rätt tid, optimerar lager och transporter, samt leder projekt inom packning, logistik och lagerhållning. Du samarbetar nära våra CMO-projektledare och bidrar i avtalsdiskussioner. Vidare driver du förbättringar för att säkerställa kostnadseffektivitet (COGS) i hela varuförsörjningskedjan. Rollen är tvärfunktionell och innebär samarbete med avdelningarna för Manufacturing, Development, Regulatory, Klinik, QA och Finans. Profil Vi söker en senior person med gedigen erfarenhet läkemedelstillverkning, särskilt inom kontraktstillverkning och intresse av att leda komplexa arbetsuppgifter inom läkemedelstillverkning och utveckling från fas III till kommersialisering. Det är meriterande om du har erfarenhet av vaccin- och biologisk läkemedelstillverkning, samt av att arbeta med produkter i sen utvecklingsfas. Utbildning, kvalifikationer och erfarenhet Universitetsutbildning inom biokemi, farmacevt, Bioteknik eller liknande naturvetenskaplig utbildning. Flerårig erfarenhet av inom läkemedelstillverkning. Erfarenhet av projektledning Erfarenhet av arbete med CMO:er och avtal. Erfarenhet av cGMP tillverkning av biologiska läkemedel och vacciner. God förmåga att kommunicera i tal och skrift (engelska o svenska). Som person är du drivande, flexibel och trivs med att kombinera operativt och strategiskt arbete. Du är noggrann, har integritet och ett prestigelöst förhållningssätt i samarbeten. Du är skicklig på att både se helheten och kritiska detaljer samt arbeta både kreativt och data-drivet. En av våra styrkor är vår förmåga att samarbeta och uppnå mål tillsammans, vi ser därför det som viktigt att du delar denna värdering. Tjänsten är en tillsvidareanställning med placering 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: 11 maj 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!

Galderma, with a science-driven portfolio across Aesthetics, Skincare, and Therapeutics, has been advancing dermatology since 1981. We’re expanding our site in Uppsala with a new state-of-the-art manufacturing facility to meet growing demand for our medicinal products. Join us in shaping the future of dermatology! We’re looking for driven, collaborative individuals who embrace learning and bring positive energy to join our inclusive, growth-oriented culture. We are now recruiting Senior Manufacturing Scientists for our Device Injectables department. About the roleAs Senior Manufacturing Scientist you’ll act as a subject matter expert (SME), leading new product implementation (NPI) into our manufacturing facility and supporting manufacturing processes. You’ll collaborate with cross-functional teams to conduct investigations, risk assessments, and ensure successful product integration. 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. Conduct in-depth root cause analysis to identify the underlying reasons for deviations and incidents, focusing on process improvement 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. SME in aseptic filling and or sterilization. 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.

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.

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!

Är du intresserad av att arbeta med laboratorie-och kvalitetsarbete? Är du strukturerad och ansvarstagande, då kan detta vara tjänsten för dig! Om tjänsten: Som Labbassistent är du delaktig i det dagliga laboratorie- och kvalitetsarbetet. Arbetet sker i nära kontakt med två kollegor på kvalitetsavdelningen. Tjänsten är ett vikariat på 3månader, med chans till förlägning. Huvudsakliga arbetsuppgifter för tjänsten: Re-validera analysmetoder för HPLC/UPLC Utföra och dokumentera validering Utföra analyser enligt uppsatta krav Vara behjälplig på flera arbetsmoment inom området. Vem är du? Som person är du noggrann, strukturerad, målorienterad och strävar efter att skapa förbättringar. Andra viktiga egenskaper är du är ansvarstagande och har ett stort öga för detaljer. Krav för tjänsten: Relevant arbetslivserfarenhet från laborativt arbete Erfarenhet inom HPLC / UPLC Körkort och tillgång till bil (kollektivtrafik är ej möjlig) Meriterande: Erfarenhet inom Waters & Empower Validering av analysmetoder Högskoleutbildning inom relevant område För resor till och från arbetsplatsen krävs körkort och tillgång till bil. Omfattning: Heltid, långsiktigt behov, arbetet sker dagtid. Ansökan Varmt välkommen med din ansökan via ansökningslänk nedan! Ansökningarna behandlas löpande och konfidentiellt. Observera att vi ej har möjlighet att behandla ansökningar som inkommer via mail eller andra kanaler. Vid frågor om tjänsten når du oss under vardagar, kl. 08-17 på 042-21 02 99. Läs gärna mer om oss på www.processbemanning.se.

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.

Är du intresserad av att arbeta med laboratorie-och kvalitetsarbete? Är du strukturerad och ansvarstagande, då kan detta vara tjänsten för dig! Om tjänsten: Som Labbassistent är du delaktig i det dagliga laboratorie- och kvalitetsarbetet. Arbetet sker i nära kontakt med två kollegor på kvalitetsavdelningen. Tjänsten är ett vikariat på 3månader, med chans till förlägning. Huvudsakliga arbetsuppgifter för tjänsten: Re-validera analysmetoder för HPLC/UPLC Utföra och dokumentera validering Utföra analyser enligt uppsatta krav Vara behjälplig på flera arbetsmoment inom området. Vem är du? Som person är du noggrann, strukturerad, målorienterad och strävar efter att skapa förbättringar. Andra viktiga egenskaper är du är ansvarstagande och har ett stort öga för detaljer. Krav för tjänsten: Relevant arbetslivserfarenhet från laborativt arbete Erfarenhet inom HPLC / UPLC Körkort och tillgång till bil (kollektivtrafik är ej möjlig) Meriterande: Erfarenhet inom Waters & Empower Validering av analysmetoder Högskoleutbildning inom relevant område För resor till och från arbetsplatsen krävs körkort och tillgång till bil. Omfattning: Heltid, långsiktigt behov, arbetet sker dagtid. Ansökan Varmt välkommen med din ansökan via ansökningslänk nedan! Ansökningarna behandlas löpande och konfidentiellt. Observera att vi ej har möjlighet att behandla ansökningar som inkommer via mail eller andra kanaler. Vid frågor om tjänsten når du oss under vardagar, kl. 08-17 på 042-21 02 99. Läs gärna mer om oss på www.processbemanning.se.