{"data":{"id":182135,"slug":"quality-assurance-specialist-3","type":"job","title":"Quality Assurance Specialist","description":"QA Specialist - Sweden Biomanufacturing Center - Consulting Position - 11 months\n\nOur production facility in S\u00f6dert\u00e4lje, Sweden Biomanufacturing Center (SBC), is a central part of AstraZeneca's strategy for manufacturing, quality assurance, and delivery of biopharmaceuticals. The site is undergoing an exciting expansion program with the establishment of new production facilities and production lines, enabling increased production and launch of the company's new medicines.\n\nAt SBC, we collaborate closely, look after each other and our patients. Here we shape the future of medicine by producing and delivering advanced, sustainable biopharmaceuticals while serving as a launch site for new products. We operate in a multicultural and global environment where digital solutions, our LEAN culture, and sustainability focus drive us forward. With us, you can design your own path, drive your development, and build your career.\n\nTo our Quality Operations team within Quality Assurance Biologics, we are now seeking a team member with the QA Specialist profile. Welcome to us where everyone feels a personal connection to the people we impact. We are committed to delivering the highest quality, from research in our laboratories to our large manufacturing facilities.\n\nYour Role\n\nYou have delegated responsibility for ensuring products maintain the correct quality and meet set requirements while becoming an important part of Quality's aseptic oversight. You will support the entire manufacturing and supply chain where you are expected to act as a quality leader by coaching and serving as an expert on GMP and quality matters broadly, both within QA and in cross-functional work.\n\nWe work closely with production and together with other support functions to support the factory's deliveries by contributing the quality perspective. You will participate in investigations of complex deviations\/complaints, contribute to various types of exciting projects and improvement efforts, and represent your operational area during regulatory inspections.\n\nYou have a broad network within SBC. You work independently with varying tasks in a rapidly changing environment. Therefore, you need to maintain structure in your work while remaining flexible when conditions change.\n\nWe require that you have:\n\nA natural science university or college degree of at least 240 credits (160 points), including 7.5 credits (5 points) in microbiology.\nGood knowledge of pharmaceutical manufacturing according to applicable regulations and Good Manufacturing Practice (GMP)\nVery good knowledge of Swedish and English, both spoken and written\nMeritorious: experience with release of sterile products\nMeritorious: experience in quality assurance in the pharmaceutical industry and quality control of pharmaceuticals\n\nWe would appreciate if you have an interest in technology, systems, and processes.\n\nTo succeed in the role, you are a driven and solution-oriented person who thrives with a large network and broad collaboration across different functions. You are skilled at seeing the bigger picture and switching between long and short deadlines. You communicate in a good, trustworthy manner. Furthermore, you possess the ability to make well-founded decisions based on risk assessments and a balanced combination of scientific facts and regulations, and can justify these in a pedagogical way.\n\nAre you ready to contribute new ideas and insights to our team? Perfect! We look forward to your application.\n\nMore information about Sweden Biomanufacturing Center:\nhttps:\/\/youtu.be\/OSj8XzlKvsM","language":"sv","is_translated":true,"title_original":"Quality Assurance Specialist","description_original":"QA Specialist - Sweden Biomanufacturing Center - Konsultuppdrag - 11 m\u00e5nader\nV\u00e5r produktionsenhet i S\u00f6dert\u00e4lje, Sweden Biomanufacturing Center (SBC) \u00e4r en central del av AstraZenecas strategi f\u00f6r produktion, kvalitetss\u00e4kring och leverans av biologiska l\u00e4kemedel. Siten genomg\u00e5r ett sp\u00e4nnande expansionsprogram med etablering av nya produktionslokaler och produktionslinjer, vilket m\u00f6jligg\u00f6r ut\u00f6kad produktion och lansering av f\u00f6retagets nya l\u00e4kemedel.\nP\u00e5 SBC har vi ett n\u00e4ra samarbete, tar hand om varandra och v\u00e5ra patienter. H\u00e4r formar vi framtidens medicin genom att producera och leverera avancerade, h\u00e5llbara biologiska l\u00e4kemedel samtidigt som vi agerar lanseringssite f\u00f6r nya produkter. Vi verkar i en m\u00e5ngkulturell och global milj\u00f6 d\u00e4r digitala l\u00f6sningar, v\u00e5r LEAN-kultur och h\u00e5llbarhetsfokus driver oss fram\u00e5t. Hos oss f\u00e5r du designa din egen v\u00e4g, driva din utveckling och bygga din karri\u00e4r.\nTill Quality Operations inom Quality Assurance Biologics s\u00f6ker vi nu medarbetare med profilen QA Specialist. V\u00e4lkommen till oss d\u00e4r alla k\u00e4nner en personlig koppling till de m\u00e4nniskor vi p\u00e5verkar. Vi \u00e4r fast beslutna att leverera h\u00f6gsta kvalitet, fr\u00e5n forskning i v\u00e5ra laboratorier till de stora tillverkningsenheterna.\nDin roll\nDu har ett delegerat ansvar f\u00f6r att produkterna h\u00e5ller r\u00e4tt kvalit\u00e9 och uppfyller st\u00e4llda krav samtidigt som du blir en viktig del av Qualitys aseptiska oversight. Du kommer att st\u00f6dja hela tillverknings- och f\u00f6rs\u00f6rjningskedjan d\u00e4r du f\u00f6rv\u00e4ntas agera som kvalitetsledare genom att coacha och agera som expert avseende GMP och kvalitetsfr\u00e5gor i stort, b\u00e5de inom QA men ocks\u00e5 i det tv\u00e4rfunktionella arbetet.\nVi arbetar n\u00e4ra produktionen och tillsammans med \u00f6vriga st\u00f6dfunktioner f\u00f6r att st\u00f6dja fabrikens leveranser genom att bidra med kvalitetsaspekten. Du deltar i utredningar av komplexa avvikelser\/reklamationer, medverkar i olika typer av sp\u00e4nnande projekt och f\u00f6rb\u00e4ttringsarbeten samt representerar ditt verksamhetsomr\u00e5de vid myndighetsinspektioner.\nDu har ett brett kontaktn\u00e4t inom SBC. Du arbetar sj\u00e4lvst\u00e4ndigt med varierande arbetsuppgifter i en snabbt f\u00f6r\u00e4nderlig milj\u00f6. D\u00e4rf\u00f6r beh\u00f6ver du h\u00e5lla en struktur i arbetet men \u00e4nd\u00e5 kunna vara flexibel n\u00e4r f\u00f6ruts\u00e4ttningarna \u00e4ndras.\nVi f\u00f6ruts\u00e4tter att du har f\u00f6ljande:\nNaturvetenskaplig universitets- eller h\u00f6gskoleexamen om minst 240 hp (160 po\u00e4ng), inklusive 7,5hp (5p) mikrobiologi.\nGoda kunskaper om l\u00e4kemedelsframst\u00e4llning enligt g\u00e4llande regelverk och Good Manufacturing Practice (GMP)\nMycket goda kunskaper i svenska och engelska, b\u00e5de i tal och skrift\nMeriterande: erfarenhet fr\u00e5n frisl\u00e4ppning av sterila produkter\nMeriterande: erfarenhet av kvalitetss\u00e4kring i l\u00e4kemedelsindustrin och kvalitetskontroll av l\u00e4kemedel\n\nVi ser g\u00e4rna att du har ett intresse f\u00f6r teknik, system och process.\nF\u00f6r att lyckas i rollen \u00e4r du en driven och l\u00f6sningsorienterad person som trivs med ett stort kontaktn\u00e4t och bred samverkan inom olika funktioner. Du \u00e4r skicklig p\u00e5 att se helhetsperspektiv och v\u00e4xla mellan l\u00e5nga och korta deadlines. Du kommunicerar p\u00e5 ett bra, f\u00f6rtroendeingivande s\u00e4tt. Vidare besitter du f\u00f6rm\u00e5gan att fatta v\u00e4lgrundade beslut baserade p\u00e5 riskbed\u00f6mningar och en balanserad kombination av vetenskapliga fakta och regelverk samt kunna motivera dessa p\u00e5 ett pedagogiskt s\u00e4tt.\n\u00c4r du redo att bidra med nya id\u00e9er och insikter till v\u00e5rt team? Perfekt! V\u00e4lkommen med din ans\u00f6kan.\nMer information om Sweden Biomanufacturing Center:\n\u201dSweden Biomanufacturing Center\u201d: https:\/\/youtu.be\/OSj8XzlKvsM","price":null,"currency":"SEK","status":"active","noindex":true,"location":{"address":"Astraall\u00e9n 3","full_address":null,"city":"S\u00d6DERT\u00c4LJE","country":"SE","latitude":59.180550284787,"longitude":17.674664817053},"metadata":{"region":"Stockholms l\u00e4n","duration":"6 m\u00e5nader \u2013 upp till 12 m\u00e5nader","employer":"Tessero Sweden AB","postcode":"15257","positions":1,"profession":"Kvalitetsrevisor","salary_type":"Fast m\u00e5nads- vecko- eller timl\u00f6n","scope_of_work":"100\u2013100 %","working_hours":"Heltid","employment_type":"temporary","occupation_field":"Administration, ekonomi, juridik","employer_workplace":"AstraZeneca","translation_status":"done","experience_required":true,"employment_type_label":"Tidsbegr\u00e4nsad anst\u00e4llning"},"user_id":null,"is_sponsored":false,"views_count":0,"ai_views_count":1,"ai_vendor_counts":{"anthropic":1},"visibility":"public","submission_source":null,"submission_ai_name":null,"has_owner_email":true,"can_contact_owner":true,"phone":null,"owner_email":"nicolina.andersson@tesserogroup.com","images":[],"published_at":"2026-09-01T14:12:35+00:00","expires_at":"2026-09-11T23:59:59+00:00","created_at":"2026-09-02T03:16:42+00:00","updated_at":"2026-09-02T04:01:28+00:00"}}