Swedish Match is dedicated to the improvement of public health by offering attractive alternatives to cigarettes. Some of our well-known brands are ZYN (nicotine pouches) and General (Snus). The company became part of Philip Morris International in 2023, and its products are now the cornerstone of the global and newly formed Category for Oral Smoke-free Products. The Role The role is a part of the Regulatory & Scientific Affairs/Analytical Science department in Stockholmwith responsibility for meeting Swedish Match’s and regulatory authorities' needs for chemical data on raw materials and products. In practice, this means quality control of the company's commercial products and those under development, primarily within smokefree product lines. The role involves tasks spanning the entire process—from receiving, handling, and processing samples to conducting analyses and shipping samples to internal customers. Responsibilities are rotated within the team, offering a broad range of tasks and providing insights into Swedish Match's entire operations. The role is integrated into a team of six individuals who uphold strong work ethics and contribute to an excellent work environment. The team characterizes their culture as friendly, social, and supportive. Work is carried out at Swedish Match office in Zinkensdam, Stockholm. Responsibilities: Perform, evaluate, and approve routine chemical analyses. Register samples in LIMS and handle logistics for shipping samples between internal sites globally. Sample preparation in the form of receiving, grinding and preparation. Support laboratory operations with tasks such as procurement and health and safety measures. Take responsibility for instrument validation, maintenance, troubleshooting, and contact with equipment suppliers. Initiate and implement method improvements and efficiency enhancements. The Candidate This role offers an exciting opportunity for someone who enjoys practical work with varied tasks. You will work cross-functionally and be part of a close-knit team. Swedish Match offers excellent working conditions, flexibility, and a supportive work environment. At times you will work hard, but you will never be alone, and we guarantee a social and enjoyable workplace. We place significant emphasis on personal qualities to ensure a strong cultural fit. Qualifications and Experience BSc in biomedical science, chemistry, biology or equivalent. Experience in laboratory work within the pharmaceutical, food, or environmental sectors is an advantage. Experience from working in LIMS is a plus. Experience writing reports and method descriptions is desirable. Experience in method development and instrument validation is a plus. Proficiency in Swedish and English, both spoken and written, is required. Personal Attributes Strong communication skills, both verbal and written. A collaborative team player who thrives in group settings. Ability to manage multiple parallel tasks, especially during busy periods. Application Join Swedish Match and become part of a dynamic team in a role that offers variety, collaboration, and personal growth. In this recruitment Swedish Match collaborates with SallyQ. For any questions please reach out to Sandra Bydell Sveder, Senior Recruitment Consultant at SallyQ, 076-319 96 88, [email protected]. Applications will be assessed continuously and will be accepted until the 11th of February.

Job description: We are looking for a full time senior analytical engineer to join and strengthen the QC team which consists of one scientist, 2 analytical engineers and 1 process technician. The QC team is part of the larger GMP operations team consisting of a production team, QA managers, facility manager, application specialist, for a total of 20 colleagues. You will be involved in the setup, validation and execution of QC methods for the analysis and release of ATMP products, to be used in clinical trials. You will also take a leading role in deviation investigations and review of documentation. Experience of cell culture, flow cytometry, potency assays, ddPCR, qPCR, mycoplasma, sterility and endotoxin tests would be a significant asset; particularly in the context of ATMP analysis. Knowledge of aseptic manufacturing techniques is desirable. Prior experience working in a GMP environment is essential for the role. You must be capable of working as part of a team and demonstrate initiative to drive projects forward. As the company and team is very international and the business language is English, excellent English communication skills is required. The role is suited to experienced and motivated professionals with a drive to lead and execute by action. What we are looking for: • Experience working according to GMP.• Quality control experience in the cell therapy or ATMP space.• Significant and relevant experience in instrument and method validation.• Experienced in writing and leading deviation investigations, CC and CAPA’s.• Good grasp of the underlying biology related to cell engineering.• Experience in microbiology.• Fluent written and spoken English. We offer: An international workplace, with plenty of variety in the job, interaction with all other Anocca employees and the opportunity to work at the exciting intersection of biotechnology and medicine. Please note that we contact candidates that we would like to invite for an interview within 3 weeks after the advertisement has closed. Unsuccessful candidates will not be contacted.Compensation Monthly salaryTier 1 occupational pension planWellness grantFlexible work hours When to apply:Last day to apply 2025-03-31EmployerAnocca AB(org.nr 556946-2384)

We are a young, fast-growing company with an agile, cross-functional work environment. We promise you open, respectful, and prestige-free colleagues and a leadership team believing in our ability to grow together. Come and contribute with your experience in product development and make our journey yours. Your Role Our products are based on the superRCA technology, which offers ultra-high sensitivity detection of multiple mutation targets simultaneously in liquid biopsies. We have developed mutation targets for both Leukemia as well as solid tumors, and are currently offering standard research kits, custom products, and research analysis services. We are now transitioning from a start-up phase to a scale-up phase and require further focus on verification and validation of our products. You will lead verification studies and analytical performance evaluations, for our research-use and diagnostic products. You will set the requirements, refine and further develop the protocols, and ensure that the documentation is accurate and fit for purpose. We are a small team, and you will collaborate cross-functionally within the company with the aim of translating research into scalable, market-ready products. Your main responsibilities will include: Designing and leading verification and validation studies, including analytical performance evaluations, for research-use and diagnostic products. Define performance requirements, refine existing protocols and define new, when needed, as well as ensure that the documentation is accurate and fit for purpose. Preparing documentation to support in vitro diagnostic device (IVD) registration in compliance with applicable regulations and guidelines, in collaboration with the RA/QA and Product Development manager. Assist in areas such as requirement management, change management, and risk management. In collaboration with statistical expertise and R&D colleagues, evaluate performance studies and reports. You will report to the Product Development Manager and be part of our core team, playing a critical role in making our liquid biopsy and mutation detection technology accessible to clinicians and researchers. We mentioned that we are on a start-up journey, meaning we adapt quickly, so your tasks may evolve as we grow. We are located in Uppsala Science Park, where we have gathered all our business functions. Your Profile We’re looking for a structured, goal-oriented individual committed to making a difference. You should have experience of leading activities, planning effectively, and delivering results independently. We also hope you are a collaborative team player who strives for unified success, but most importantly, we hope you are yourself. We are a team of individuals, and our differences are what make us a dream team. Qualifications: A university degree in Molecular/Cell Biology, Biotechnology, Biochemistry, or a related field. 3-5years of experience in product development, particularly in verification and validation within a regulated environment. Proficiency in report writing and familiarity with statistical methods and data analysis. Experience collaborating with statistical experts and designing performance studies according to standards and guidelines, such as the CLSI guidelines or similar. Professional fluency in English, both written and verbal. Experience from flow cytometry and molecular biology techniques, including PCR and other DNA amplification methods is a plus. Application Join us and be part of a transformative journey in healthcare! We are accepting applications until the 6nd ofFebruary. If you have any questions regarding the position, please do not hesitate to reach out to Sandra Bydell Sveder, Recruitment Consultant ([email protected] or 076-319 96 88).

Är du tillgänglig omgående och söker en arbetsplats där du får utföra kemiskt laborativt arbete, samarbeta med trevliga arbetskamrater och vara en del i ett förbättringsarbete? Recipharm erbjuder en stimulerande tjänst med stora utvecklingsmöjligheter! Om tjänsten Det här är ett konsultuppdrag på heltid som varar i 8 månader. Du blir anställd av Bravura och arbetar som konsult hos Recipharm. Det finns goda möjligheter till förlängning av uppdraget. Om företaget Recipharm är ett svenskt, ledande CDMO-företag (Contract Development and Manufacturing Organisation) inom läkemedelsindustrin och har nära 9 000 anställda. Recipharm erbjuder tillverkningstjänster av läkemedel i olika former, produktion av material till kliniska prövningar och API:er, farmaceutisk produktutveckling samt utveckling och tillverkning av medel för läkemedelsadministration. Recipharm tillverkar flera hundra olika produkter åt såväl stora läkemedelsföretag som mindre utvecklingsbolag. Bolaget omsätter cirka 11 miljarder kronor per år och har utvecklings- och tillverkningsanläggningar i Frankrike, Indien, Israel, Italien, Portugal, Spanien, Storbritannien, Sverige, Tyskland och USA med huvudkontor i Stockholm, Sverige. Inom Recipharm Uppsala är QC uppdelat i 3 grupper varav två arbetar med rutinanalyser. Nu söker Recipharm två labbingenjörer, en till vardera analysteam. Arbetsuppgifter Som labbingenjör tillhör du avdelningen Quality Control. QC är en del i Recipharms produktionsflöde som utför kemisk analys av råvaror, processprover, intermediat och slutprodukter, förpackningskontroll samt disposition av råvaror och förpackningsmaterial. Inom avdelningen hanteras också stab- och hållbarhetsprover. I rollen ingår även att fullgöra tilldelat ansvar för metoder, utrustning och lokaler, samt att använda vetenskapligt sund metodik och arbeta i enlighet med myndigheters kvalitets- och GMP-förväntningar samt företagets kvalitetsstandarder. Du kan även komma att delta i kvalificeringsarbete och transfer av metoder. Arbetet utförs i enlighet med och styrs av GMP varför arbetet har väldigt tydliga ramar för hur det får utföras. Den här rollen är mycket meriterande för dig som vill bredda din kompetens. Här ges du möjlighet att ta del av flera olika typer av analytiska metoder, som exempelvis, kromatografi, titreringar samt våtkemiska metoder. Du får en gedigen introduktion hos Recipharm där du stegvis lär dig de olika arbetsuppgifterna. Utbildning, erfarenhet och personliga egenskaper Krav: • Avslutad akademisk utbildning inom kemi, biologi, naturvetenskap alternativt farmaceutisk utbildning • Minst 2 års arbetslivserfarenhet från liknande roll i ett GMP styrt QC-laboratorium • Erfarenhet av utförande av våtkemiska analyser samt tolkning av farmakopéer och/eller inom titrering, frisättning och UV. • Du behärskar svenska och engelska flytande i tal och skrift Meriterande: • Erfarenhet av rapportering i LIMS • Erfarenhet av HPLC För att passa för den här rollen tror vi att du som söker besitter analytisk kompetens och har förmågan att självständigt driva ditt arbete framåt inom satta tidsramar. Då rollen innebär ett stort ansvar i att arbeta med substanser som är avgörande för liv och hälsa är det väldigt viktigt att du är noggrann, strukturerad och flexibel. Slutligen har du en god samarbetsförmåga men kan hantera dina arbetsuppgifter både självständigt och i grupp. Att vara en del i Recipharm är synonymt med att vara en del i en miljö med goda utsikter. Recipharms världsomfattande utsträckning innebär att där finns en stor variation av vägar att välja som ett led i din framtida utveckling. Övrig information Start: Omgående Plats: Uppsala Lön: Enligt överenskommelse Vi använder en kompetensbaserad metodik i alla rekryteringsprocesser för att säkerställa fördomsfria urval. Vi jobbar också med löpande urval, vilket innebär att vi tar ner annonsen när tillräckligt många kandidater har ansökt. Om du blir aktuell för tjänsten kommer vi att kontakta dig för en första telefonintervju. Oavsett om du går vidare i processen eller inte så kommer du att få återkoppling på din ansökan. Har du frågor om tjänsten eller kring din ansökan är du välkommen att kontakta vår support genom att maila till [email protected] eller ringa till nummer 010-171 47 10 så hjälper vi dig. Ange vilken tjänst det gäller.Vi rekommenderar att du skickar in din ansökan omgående då vi gör ett löpande urval. Välkommen med din ansökan! Sista ansökningsdatum är 2025-01-17.