{"data":{"id":210932,"slug":"qa-specialist-gmp-extempore-4","type":"job","title":"QA Specialist \u2013 GMP & Extemporaneous","description":"Do you want to work with quality in an operation where pharmaceutical manufacturing, innovation, and regulatory requirements converge?\nAtrimusRx is seeking a QA Specialist for our growing extemporaneous pharmacy operation in Sollentuna.\nWith us, you'll work closely with operations and help develop quality practices in personalized pharmaceutical manufacturing, extemporaneous compounding, and new manufacturing techniques.\nThis is a role for someone with QA and GMP experience who wants to work in an environment where quality isn't just about maintaining existing processes, but also about developing them.\n\nAbout the Role\nAs a QA Specialist, you'll be a key part of our quality efforts and work closely with pharmacists, production, development, and management.\nYour responsibilities will include:\ndevelopment and maintenance of quality systems\nworking with GMP and regulatory requirements for pharmaceutical manufacturing\ncreating, reviewing, and updating SOPs and other quality documentation\ndeviation handling, CAPA, and change control\nrisk assessments and Quality Risk Management\nqualification and validation of equipment, processes, and methods\nreview of manufacturing and quality documentation\nvendor assessments and quality agreements\ntraining staff in GMP and quality\ninternal inspections and quality monitoring\npreparations for and participation in regulatory inspections\ndevelopment and improvement of processes in our extemporaneous operations\n\nDepending on your experience and expertise, the role can also develop into greater quality responsibility within the operation.\n\nWho Are We Looking For?\nWe're seeking someone with relevant QA and GMP experience in pharmaceutical manufacturing.\nYou may currently work as, for example:\nQA Specialist\nSenior QA Specialist\nQA Manager\nValidation Specialist\nQuality Manager\nProduction Pharmacist\nPharmacist in extemporaneous compounding\nor in a corresponding quality function in the pharmaceutical industry\n\nWe would be pleased if you have experience from one or more of the following areas:\npharmaceutical manufacturing\nextemporaneous compounding\npharmaceutical industry\nhospital pharmacy with manufacturing\nvalidation and qualification\ndeviation handling and CAPA\nchange control\nQuality Risk Management\nregulatory inspections\nworking with quality systems in regulated operations\n\nPharmaceutical education is a merit, especially if you are a pharmacist or pharmacy technician with experience in pharmaceutical manufacturing or extemporaneous compounding.\nFor candidates with the right education and experience, there may be an opportunity to take on formal GMP responsibility within the operation in the future.\n\nAs a Person\nWe believe you are structured, thorough, and quality-minded, but also pragmatic and solution-oriented.\nYou need to understand both regulatory requirements and the practical operations behind them.\nWe especially appreciate people who:\nsee quality as a support for operations, not as an administrative function separate from the business\ndare to identify problems and drive improvements\ncan work independently and take responsibility\nthrive with short decision-making paths\nenjoy building structures and processes\nhave high integrity and a strong quality mindset\nare curious about new working methods and techniques\n\nWhy AtrimusRx?\nAtrimusRx works with pharmaceutical supply, medicine shortages, licensed medicines, and extemporaneous compounding.\nWithin our extemporaneous operations, we work with personalized pharmaceutical manufacturing and develop new ways to produce medicines in strengths and formulations tailored to patient needs.\nWe work with, among other things, 3D printing of pharmaceuticals, which means quality and regulatory matters are an integrated part of both development and manufacturing.\nWith us, you'll have the opportunity to work in an operation where QA is closely linked to development, production, and innovation.\nYou'll be part of a smaller, entrepreneurial company with short decision-making paths and great ambitions.\n\nPractical Information\nLocation: Sollentuna\nFull-time\nStart: By agreement\n\nApplication Process\nThe recruitment process begins with two tests:\nA personality test that takes approximately 2 minutes.\nA cognitive test that takes approximately 12 minutes. The second test is sent 24 hours after the first test is completed.\n\nOnce both tests are completed, send your CV to jobb@atrimusrx.se.\nAll steps must be completed in the specified order. Applications that do not follow this procedure will not be considered.\nThoroughness, attention to detail, and the ability to follow instructions are critical qualities for this position. The application process is therefore part of our initial screening.\nSelection and interviews are ongoing. The position may be filled before the final application deadline.\nWe do not welcome contact from media sales representatives, recruitment consultants, and similar.","language":"sv","is_translated":true,"title_original":"QA Specialist \u2013 GMP & Extempore","description_original":"Vill du arbeta med kvalitet i en verksamhet d\u00e4r l\u00e4kemedelstillverkning, innovation och regulatoriska krav m\u00f6ts?\nAtrimusRx s\u00f6ker en QA Specialist till v\u00e5r v\u00e4xande extemporeverksamhet i Sollentuna.\nHos oss f\u00e5r du arbeta n\u00e4ra verksamheten och vara med och utveckla kvalitetsarbetet inom individanpassad l\u00e4kemedelstillverkning, extempore och nya tillverkningstekniker.\nDet h\u00e4r \u00e4r en roll f\u00f6r dig som har erfarenhet av QA och GMP och som vill arbeta i en milj\u00f6 d\u00e4r kvalitet inte bara handlar om att f\u00f6rvalta befintliga processer, utan ocks\u00e5 om att vara med och utveckla dem.\nOm rollen\nSom QA Specialist blir du en central del av v\u00e5rt kvalitetsarbete och arbetar n\u00e4ra farmaceuter, produktion, utveckling och ledning.\nDina arbetsuppgifter kommer bland annat att omfatta:\nutveckling och f\u00f6rvaltning av kvalitetssystem\narbete med GMP och regulatoriska krav f\u00f6r l\u00e4kemedelstillverkning\nframtagning, granskning och uppdatering av SOP och annan kvalitetsdokumentation\navvikelsehantering, CAPA och change control\nriskbed\u00f6mningar och Quality Risk Management\nkvalificering och validering av utrustning, processer och metoder\ngranskning av tillverknings- och kvalitetsdokumentation\nleverant\u00f6rsbed\u00f6mningar och kvalitetsavtal\nutbildning av personal inom GMP och kvalitet\negeninspektioner och kvalitetsuppf\u00f6ljning\nf\u00f6rberedelser inf\u00f6r och deltagande vid myndighetsinspektioner\nutveckling och f\u00f6rb\u00e4ttring av processer inom v\u00e5r extemporeverksamhet\n\nBeroende p\u00e5 din erfarenhet och kompetens kan rollen \u00e4ven utvecklas till ett st\u00f6rre kvalitetsansvar inom verksamheten.\nVem s\u00f6ker vi?\nVi s\u00f6ker dig som har relevant erfarenhet av QA och GMP inom l\u00e4kemedelstillverkning.\nDu kan idag arbeta som exempelvis:\nQA Specialist\nSenior QA Specialist\nQA Manager\nvalideringsspecialist\nkvalitetsansvarig\nproduktionsfarmaceut\nfarmaceut inom extemporetillverkning\neller i en motsvarande kvalitetsfunktion inom l\u00e4kemedelsindustrin\n\nVi ser g\u00e4rna att du har erfarenhet fr\u00e5n n\u00e5got eller flera av f\u00f6ljande omr\u00e5den:\nl\u00e4kemedelstillverkning\nextemporetillverkning\nl\u00e4kemedelsindustri\nsjukhusapotek med tillverkning\nvalidering och kvalificering\navvikelsehantering och CAPA\nchange control\nQuality Risk Management\nmyndighetsinspektioner\narbete med kvalitetssystem inom reglerad verksamhet\n\nFarmaceutisk utbildning \u00e4r meriterande, s\u00e4rskilt om du \u00e4r apotekare eller receptarie med erfarenhet av l\u00e4kemedelstillverkning eller extempore.\nF\u00f6r kandidater med r\u00e4tt utbildning och erfarenhet kan det \u00e4ven finnas m\u00f6jlighet att p\u00e5 sikt ta ett formellt GMP-ansvar inom verksamheten.\nSom person\nVi tror att du \u00e4r strukturerad, noggrann och kvalitetsmedveten, men samtidigt pragmatisk och l\u00f6sningsorienterad.\nDu beh\u00f6ver kunna f\u00f6rst\u00e5 b\u00e5de regulatoriska krav och den praktiska verksamheten bakom dem.\nVi uppskattar s\u00e4rskilt personer som:\nser kvalitet som ett st\u00f6d f\u00f6r verksamheten och inte som en administrativ funktion vid sidan av\nv\u00e5gar identifiera problem och driva f\u00f6rb\u00e4ttringar\nkan arbeta sj\u00e4lvst\u00e4ndigt och ta ansvar\ntrivs med korta beslutsv\u00e4gar\ntycker om att bygga strukturer och processer\nhar h\u00f6g integritet och ett starkt kvalitetst\u00e4nk\n\u00e4r nyfikna p\u00e5 nya arbetss\u00e4tt och tekniker\n\nVarf\u00f6r AtrimusRx?\nAtrimusRx arbetar med l\u00e4kemedelsf\u00f6rs\u00f6rjning, l\u00e4kemedelsbrist, licensl\u00e4kemedel och extemporetillverkning.\nInom v\u00e5r extemporeverksamhet arbetar vi med individanpassad l\u00e4kemedelstillverkning och utvecklar nya m\u00f6jligheter att tillverka l\u00e4kemedel i styrkor och beredningsformer anpassade efter patientens behov.\nVi arbetar bland annat med 3D-printing av l\u00e4kemedel, vilket inneb\u00e4r att kvalitet och regulatoriska fr\u00e5gor \u00e4r en integrerad del av b\u00e5de utveckling och tillverkning.\nHos oss f\u00e5r du d\u00e4rf\u00f6r m\u00f6jlighet att arbeta i en verksamhet d\u00e4r QA \u00e4r n\u00e4ra kopplat till utveckling, produktion och innovation.\nDu blir en del av ett mindre och entrepren\u00f6riellt bolag med korta beslutsv\u00e4gar och stora ambitioner.\nPraktisk information\nPlacering: Sollentuna\nOmfattning: Heltid\nTilltr\u00e4de: Enligt \u00f6verenskommelse\nAns\u00f6kningsf\u00f6rfarande\nRekryteringsprocessen inleds med tv\u00e5 tester:\nEtt personlighetstest som tar cirka 2 minuter.\nEtt kognitivt test som tar cirka 12 minuter. Det andra testet skickas 24 timmar efter att det f\u00f6rsta testet har slutf\u00f6rts.\n\nN\u00e4r b\u00e5da testerna \u00e4r genomf\u00f6rda ska du skicka ditt CV till jobb@atrimusrx.se.\nSamtliga steg ska genomf\u00f6ras i angiven ordning. Ans\u00f6kningar som inte f\u00f6ljer denna rutin kommer inte att beaktas.\nNoggrannhet, detaljfokus och f\u00f6rm\u00e5ga att f\u00f6lja instruktioner \u00e4r avg\u00f6rande egenskaper i tj\u00e4nsten. Ans\u00f6kningsf\u00f6rfarandet utg\u00f6r d\u00e4rf\u00f6r en del av v\u00e5rt f\u00f6rsta urval.\nUrval och intervjuer sker l\u00f6pande. Tj\u00e4nsten kan tills\u00e4ttas f\u00f6re sista ans\u00f6kningsdag.\nVi undanber oss kontakt med medias\u00e4ljare, rekryteringskonsulter och liknande.","price":null,"currency":"SEK","status":"active","noindex":true,"location":{"address":"Hammarbacken 6A","full_address":null,"city":"Sollentuna","country":"SE","latitude":59.445286370565,"longitude":17.923869409747},"metadata":{"region":"Stockholms l\u00e4n","duration":"Tills vidare","employer":"AtrimusRX AB","postcode":"19149","positions":1,"profession":"Regulatorisk handl\u00e4ggare\/Regulatory affairs specialist","salary_type":"Fast m\u00e5nads- vecko- eller timl\u00f6n","scope_of_work":"100\u2013100 %","working_hours":"Heltid","employment_type":"full_time","occupation_field":"Naturvetenskap","employer_workplace":"Atrimusrx AB","experience_required":true,"employment_type_label":"Tillsvidareanst\u00e4llning (inkl. eventuell provanst\u00e4llning)"},"user_id":null,"is_sponsored":false,"views_count":0,"ai_views_count":3,"bot_views_count":2,"ai_vendor_counts":{"openai":1,"anthropic":2},"visibility":"public","submission_source":null,"submission_ai_name":null,"has_owner_email":true,"can_contact_owner":true,"phone":null,"owner_email":"jobb@atrimusrx.se","images":[],"published_at":"2026-09-14T16:49:40+00:00","expires_at":"2026-10-14T23:59:59+00:00","created_at":"2026-09-15T03:24:42+00:00","updated_at":"2026-09-16T09:06:01+00:00"}}