{"data":{"id":206933,"slug":"produktionsingenjor-sterila-processer","type":"job","title":"Production Engineer Sterile Processes","description":"Do you want to be part of developing the future of pharmaceutical manufacturing?\nWe are seeking an engineer who wants to work with qualification, validation, and development of sterile processes and quality-critical production systems. This role suits you if you want to combine engineering, problem-solving, and regulatory requirements in an operation where quality and patient safety are central.\nAbout the Role\nAs a Production Engineer specializing in sterile processes, you will be responsible for ensuring that our quality-critical equipment and processes meet the requirements of our operations, regulatory authorities, and customers.\nAn important part of the role is to plan and conduct periodic revalidations of sterilization processes and to investigate deviations related to equipment and processes. You will work closely with production, the quality department, and other technical functions to ensure compliance with applicable regulations and continuous improvement of operations.\nAutoclaves and sterilization processes are an important specialty area, but the role also encompasses other types of production and process equipment.\nKey Responsibilities\nBe a technical specialist in sterile processes and sterilization\nPlan, conduct, evaluate, and document qualification and periodic revalidation of sterilization processes\nInvestigate deviations, conduct root cause analyses, and drive CAPA activities\nSpecify requirements, procure, and implement new production equipment\nLead\/Participate in investment and improvement projects\nEvaluate process data and identify improvement opportunities\nProvide technical support to the production organization\n\nWhat We're Looking For\nYou hold an engineering degree in chemical engineering, biotechnology, mechanical engineering, or another relevant technical field\nYou have experience from the pharmaceutical industry or other regulated operations\nYou have knowledge of GMP or other quality-controlled working methods\nYou are analytical, structured, and driven to solve complex technical problems\n\nMeritorious\nExperience with sterile processes, autoclaves, aseptic production, CIP\/SIP systems, or qualification and validation within a GMP environment.\n\nWhat We Offer\nWith us, you will have a unique opportunity to develop your specialist knowledge in a critical area of pharmaceutical manufacturing while working broadly with engineering, processes, equipment, and investments.\nYou will be an important part of an experienced team with expertise in pharmaceutical manufacturing, automation, IT, investments, and process development. We work independently within our specialist areas but collaborate closely when solving complex technical challenges.\nThe role spans from troubleshooting and qualification work to project management and implementation of new production equipment, which provides great variety in your day-to-day work and excellent opportunities for both personal and professional development.\nWelcome to become part of our team \u2013 where your expertise makes a difference!\nMeribel Pharma Solutions Meribel Pharma Solutions was founded in 2024 and is a niche, mid-sized CDMO specializing in providing customized pharmaceutical solutions to pharmaceutical companies. With headquarters in the United Kingdom and 11 facilities in Sweden, France, and Spain, we offer specialist expertise in sterile multi-dose, freeze-drying, sachets, and stick packages, as well as services to support development from concept to commercialization. We are dedicated to elevating pharmaceutical services to new heights and delivering comprehensive support through every step of a product's journey, whether the product is an oral solid dose, liquid, or semi-solid. Want to know more about us? Please visit our website: https:\/\/meribelpharma.com\/.\nWhat We Offer You:\nWith us, you will be an important part of a company on an exciting journey. Here you will work in an environment where improvement work truly makes a difference \u2013 both for the business and for your colleagues.\nA clean and structured GMP environment with stable processes.\nA team that values collaboration and development.\nA workplace where quality and safety are central, and where you have the opportunity to grow and make an impact.\nFavorable terms with collective agreement, ATK days, and wellness allowance and time off for all bank holidays.\n\nSounds interesting to you?\nFor questions about the position, contact: Stina Pernefur, Manager Production Engineering and IT mailto:Stina.Pernefur@meribelpharma.com\nFor questions about the recruitment process, contact: Sandra Lindell, HR Generalist mailto:Sandra.Lindell@meribelpharma.com\nApplication:\nSelection will be made on a rolling basis with final application deadline 2026-10-11.\nWe look forward to receiving your application!","language":"sv","is_translated":true,"title_original":"Produktionsingenj\u00f6r Sterila Processer","description_original":"Vill du vara med och utveckla framtidens l\u00e4kemedelsproduktion?\nVi s\u00f6ker en ingenj\u00f6r som vill arbeta med kvalificering, validering och utveckling av sterila processer samt kvalitetskritiska produktionssystem. Rollen passar dig som vill kombinera teknik, probleml\u00f6sning och regulatoriska krav i en verksamhet d\u00e4r kvalitet och patients\u00e4kerhet st\u00e5r i centrum.\nOm rollen\nSom Produktionsingenj\u00f6r med inriktning mot sterila processer ansvarar du f\u00f6r att s\u00e4kerst\u00e4lla att v\u00e5ra kvalitetskritiska utrustningar och processer uppfyller verksamhetens, myndigheternas och kundernas krav.\nEn viktig del av rollen \u00e4r att planera och genomf\u00f6ra \u00e5terkommande revalideringar av steriliseringsprocesser samt att utreda avvikelser kopplade till utrustningar och processer. Du arbetar n\u00e4ra produktion, kvalitetsavdelning och andra teknikfunktioner f\u00f6r att s\u00e4kerst\u00e4lla efterlevnad av g\u00e4llande regelverk och kontinuerlig utveckling av verksamheten.\nAutoklaver och steriliseringsprocesser \u00e4r ett viktigt specialistomr\u00e5de, men rollen omfattar \u00e4ven andra typer av produktions- och processutrustningar.\nArbetsuppgifter\nVara teknisk specialist inom sterila processer och sterilisering\nPlanera, genomf\u00f6ra, utv\u00e4rdera och dokumentera kvalificering samt \u00e5terkommande revalidering av steriliseringsprocesser\nUtreda avvikelser, genomf\u00f6ra grundorsaksanalyser och driva CAPA-aktiviteter\nKravst\u00e4lla, upphandla och implementera ny produktionsutrustning\nLeda\/Delta i investerings- och f\u00f6rb\u00e4ttringsprojekt\nUtv\u00e4rdera processdata och identifiera f\u00f6rb\u00e4ttringsm\u00f6jligheter\nGe tekniskt st\u00f6d till produktionsorganisationen\n\nVi s\u00f6ker dig som\nHar ingenj\u00f6rsexamen inom kemiteknik, bioteknik, maskinteknik eller annat relevant tekniskt omr\u00e5de.\nHar erfarenhet fr\u00e5n l\u00e4kemedelsindustri eller annan reglerad verksamhet\nHar kunskap om GMP eller andra kvalitetsstyrda arbetss\u00e4tt\n\u00c4r analytisk, strukturerad och drivs av att l\u00f6sa komplexa tekniska problem\n\nMeriterande\nErfarenhet av sterila processer, autoklaver, aseptisk produktion, CIP\/SIP-system eller kvalificering och validering inom GMP-milj\u00f6.\n\nVi erbjuder\nHos oss f\u00e5r du en unik m\u00f6jlighet att utveckla din specialistkunskap inom ett kritiskt omr\u00e5de f\u00f6r l\u00e4kemedelsproduktion samtidigt som du f\u00e5r arbeta brett med teknik, processer, utrustningar och investeringar.\nDu kommer att vara en viktig del av ett erfaret team med kompetens inom l\u00e4kemedelsproduktion, automation, IT, investeringar och processutveckling. Vi arbetar sj\u00e4lvst\u00e4ndigt inom v\u00e5ra specialistomr\u00e5den men samarbetar t\u00e4tt n\u00e4r vi l\u00f6ser komplexa tekniska utmaningar.\nRollen sp\u00e4nner fr\u00e5n fels\u00f6kning och kvalificeringsarbete till projektledning och implementering av ny produktionsutrustning, vilket ger en stor variation i vardagen och goda m\u00f6jligheter till b\u00e5de personlig och professionell utveckling.\nV\u00e4lkommen att bli en del av v\u00e5rt team \u2013 d\u00e4r din kompetens g\u00f6r skillnad!\nMeribel Pharma Solutions Meribel Pharma Solutions grundades 2024 och \u00e4r en nischad, medelstor CDMO som specialiserar sig p\u00e5 att tillhandah\u00e5lla skr\u00e4ddarsydda farmaceutiska l\u00f6sningar till l\u00e4kemedelsf\u00f6retag. Med huvudkontor i Storbritannien och 11 anl\u00e4ggningar i Sverige, Frankrike och Spanien erbjuder vi specialistkompetens inom sterila multidoser, frystorkning, dosp\u00e5sar och stickf\u00f6rpackningar samt tj\u00e4nster f\u00f6r att st\u00f6dja utveckling fr\u00e5n koncept till kommersialisering. Vi \u00e4r dedikerade till att lyfta l\u00e4kemedelstj\u00e4nster till nya h\u00f6jder och leverera omfattande support genom varje steg av en produkts resa, oavsett om produkten \u00e4r en oral fast dos, flytande eller halvfast. Vill du veta mer om oss, bes\u00f6k g\u00e4rna v\u00e5r hemsida: https:\/\/meribelpharma.com\/.\nVad vi erbjuder dig:\nHos oss blir du en viktig del av ett f\u00f6retag som \u00e4r p\u00e5 en sp\u00e4nnande resa. H\u00e4r f\u00e5r du arbeta i en milj\u00f6 d\u00e4r f\u00f6rb\u00e4ttringsarbete verkligen g\u00f6r skillnad \u2013 b\u00e5de f\u00f6r verksamheten och f\u00f6r dina kollegor.\nEn ren och strukturerad GMP-milj\u00f6 med stabila processer.\nEtt team som v\u00e4rdes\u00e4tter samarbete och utveckling.\nEn arbetsplats d\u00e4r kvalitet och s\u00e4kerhet st\u00e5r i centrum, och d\u00e4r du har m\u00f6jlighet att v\u00e4xa och p\u00e5verka.\nF\u00f6rm\u00e5nliga villkor med kollektivavtal, ATK-dagar och friskv\u00e5rdsbidrag och ledig alla kl\u00e4mdagar.\n\nL\u00e5ter det h\u00e4r intressant f\u00f6r dig?\nVid fr\u00e5gor om tj\u00e4nsten, kontakta: Stina Pernefur, Manager Production Engineering and IT mailto:Stina.Pernefur@meribelpharma.com\nVid fr\u00e5gor om rekryteringsprocessen, kontakta: Sandra Lindell, HR Generalist mailto:Sandra.Lindell@meribelpharma.com\nAns\u00f6kan:\nUrval sker l\u00f6pande med sista ans\u00f6kningsdag 2026-10-11.\nV\u00e4lkommen med din ans\u00f6kan!","price":null,"currency":"SEK","status":"active","noindex":true,"location":{"address":"Box 410","full_address":null,"city":"Karlskoga","country":"SE","latitude":59.3265366,"longitude":14.5267039},"metadata":{"region":"\u00d6rebro l\u00e4n","duration":"Tills vidare","employer":"Meribel Pharma Karlskoga AB","postcode":"69127","positions":1,"profession":"Produktionsingenj\u00f6r, maskin","salary_type":"Fast m\u00e5nads- vecko- eller timl\u00f6n","scope_of_work":"100\u2013100 %","working_hours":"Heltid","employment_type":"full_time","occupation_field":"Yrken med teknisk inriktning","employer_workplace":"Meribel Pharma - Karlskoga","experience_required":true,"employment_type_label":"Vanlig anst\u00e4llning"},"user_id":null,"is_sponsored":false,"views_count":0,"ai_views_count":4,"bot_views_count":2,"ai_vendor_counts":{"other":1,"openai":2,"anthropic":1},"visibility":"public","submission_source":null,"submission_ai_name":null,"has_owner_email":true,"can_contact_owner":true,"phone":null,"owner_email":"stina.pernefur@meribelpharma.com","images":[],"published_at":"2026-09-11T08:28:48+00:00","expires_at":"2026-10-11T23:59:59+00:00","created_at":"2026-09-12T03:24:38+00:00","updated_at":"2026-09-15T03:10:46+00:00"}}