{"data":{"id":157894,"slug":"senior-qp-specialist-2","type":"job","title":"Senior QP Specialist","description":"Sever Pharma Solutions is a contract developer and manufacturer specializing in highly potent pharmaceuticals. Our headquarters in Malm\u00f6 has developed and manufactured pharmaceuticals for nearly 50 years according to the rigorous standards required of pharmaceutical companies. Our customers range from large global to smaller pharmaceutical companies, and we have over 320 employees in Malm\u00f6 and the USA.\n\nWould you like to be a key person in a growing, international organization where continuous improvement and patient safety are core values? We are now seeking an experienced and engaged Senior QP Specialist who can be part of Sever Pharma Solutions' continued growth and is ready to contribute your knowledge to ongoing development and a strengthened quality culture in an organization undergoing change.\n\nThe Quality Department you will be joining consists of approximately 50 people, and you will report directly to the VP Director Quality. You will also work closely with another experienced QP.\n\nAbout the Role\nAs a QP, you will have a central and independent role responsible for ensuring that manufactured pharmaceutical products meet applicable GMP requirements, regulatory requirements, and internal quality standards before certification and release.\n\nThe role involves close collaboration with QA, QC, production, and other cross-functional groups in the organization.\n\nYour Areas of Responsibility\n\u2022 Certify and release manufactured pharmaceutical batches in accordance with applicable GMP and regulatory requirements\n\u2022 Ensure that raw materials, packaging materials, and finished products have been tested and approved according to established specifications\n\u2022 Review and approve deviations, changes, CAPA, and quality-related investigations\n\u2022 Ensure compliance with European and international regulatory requirements, including requirements from the Swedish Medical Products Agency, EMA, and FDA\n\u2022 Contribute to the development and improvement of quality processes and quality culture\n\nYour Background and Experience\n\u2022 You have an academic degree in pharmacy, chemistry, biomedicine, or similar at Master level\n\u2022 You have several years of experience as a Quality Assurance specialist, preferably also in other quality-related tasks in a GMP-governed operation\n\u2022 You are certified as a QP by the Swedish Medical Products Agency and have several years of experience in the international pharmaceutical industry, meeting the Swedish Medical Products Agency standard HSLF-FS 2021:102\n\u2022 You have an agile working style and can prioritize your tasks; you are a good and clear communicator\n\u2022 Previous experience with sterile manufacturing in the pharmaceutical industry is a plus\n\u2022 You speak and write Swedish and English fluently\n\nAs a person, you are confident, accustomed to working independently, and have the ability to make informed decisions based on your knowledge and experience. You drive your projects efficiently with continuous improvement as the goal. You have excellent collaboration skills and integrity in your role. You thrive in a developmental environment where change and improvement work are part of everyday life. You are meticulous, structured, and have a pronounced quality awareness that permeates your actions. You will be an important part of a very pleasant team in a stimulating environment where you get to participate in new development projects that often become reality in the form of state-of-the-art pharmaceuticals.\n\nWe look forward to telling you more about the position and Sever Pharma Solutions! Don't hesitate to get in touch for more information or to have your questions answered. We will review applications on an ongoing basis. Warm welcome!","language":"sv","is_translated":true,"title_original":"Senior QP Specialist","description_original":"Sever Pharma Solutions \u00e4r en kontraktsutvecklare och tillverkare specialiserad p\u00e5 h\u00f6gpotenta l\u00e4kemedel. Huvudkontoret i Malm\u00f6 har utvecklat och tillverkat l\u00e4kemedel sedan n\u00e4rmare 50 \u00e5r enligt de h\u00f6ga krav som st\u00e4lls p\u00e5 l\u00e4kemedelsf\u00f6retag. V\u00e5ra kunder \u00e4r allt fr\u00e5n stora globala till mindre l\u00e4kemedelsf\u00f6retag och vi har drygt 320 anst\u00e4llda i Malm\u00f6 och USA.\nVill du vara en viktig nyckelperson i en v\u00e4xande, internationell organisation d\u00e4r kontinuerlig f\u00f6rb\u00e4ttring och patients\u00e4kerhet \u00e4r ledord? Vi s\u00f6ker nu en erfaren och engagerad, senior QP Specialist som kan vara del i Sever Pharma Solutions forts\u00e4tta tillv\u00e4xt och d\u00e4rmed \u00e4r beredd att bidra med din kunskap till fortsatt utveckling och st\u00e4rkt kvalitetskultur i en organisation i f\u00f6r\u00e4ndring.\u00a0\nKvalitetsavdelningen som du kommer att tillh\u00f6ra, best\u00e5r av ett 50-tal personer och du kommer att rapportera direkt till VP Director Quality. Du kommer ocks\u00e5 att ha n\u00e4ra samarbete med ytterligare en erfaren QP.\u00a0\nOm rollen\nSom QP har du en central och sj\u00e4lvst\u00e4ndig roll med ansvar f\u00f6r att s\u00e4kerst\u00e4lla att tillverkade l\u00e4kemedelsprodukter uppfyller g\u00e4llande GMP-krav, regulatoriska krav och interna kvalitetsstandarder innan certifiering och frisl\u00e4ppning.\nRollen inneb\u00e4r n\u00e4ra samarbete med QA, QC, produktion och andra tv\u00e4rfunktionella grupper i verksamheten.\nDina ansvarsomr\u00e5den\nCertifiera och frisl\u00e4ppa tillverkade l\u00e4kemedelsbatcher i enlighet med g\u00e4llande GMP och regulatoriska krav\u00a0\nS\u00e4kerst\u00e4lla att r\u00e5varor, f\u00f6rpackningsmaterial och f\u00e4rdiga produkter har testats och godk\u00e4nts enligt fastst\u00e4llda specifikationer\u00a0\nGranska och godk\u00e4nna avvikelser, f\u00f6r\u00e4ndringar, CAPA och kvalitetsrelaterade utredningar\u00a0\nS\u00e4kerst\u00e4lla efterlevnad av europeiska och internationella regulatoriska krav, inklusive krav fr\u00e5n L\u00e4kemedelsverket, EMA och FDA\u00a0\nBidra till utveckling och f\u00f6rb\u00e4ttring av kvalitetsprocesser och kvalitetskultur\u00a0\n\nDin bakgrund och erfarenhet\nDu har en akademisk examen inom farmaci, kemi, biomedicin eller liknande p\u00e5 Master niv\u00e5\nDu har flera \u00e5rs erfarenhet som Quality Assurance specialist men g\u00e4rna \u00e4ven inom andra kvalitetsrelaterade uppgifter i en GMP styrd verksamhet\nDu \u00e4r certifierad QP av l\u00e4kemedelsverket och har fler\u00e5rig erfarenhet inom internationell l\u00e4kemedelsindustri och uppfyller L\u00e4kemedelsverkets standard HSLF-FS 2021:102\nDu har ett agilt arbetss\u00e4tt och kan prioritera dina arbetsuppgifter och du \u00e4r en god och tydlig kommunikat\u00f6r\nTidigare erfarenhet av steril tillverkning inom l\u00e4kemedelsindustrin \u00e4r meriterande\nDu talar och skriver svenska och engelska flytande\n\nSom person \u00e4r du trygg, van att arbeta sj\u00e4lvst\u00e4ndigt och har f\u00f6rm\u00e5ga att fatta egna beslut grundade p\u00e5 din kunskap och dina erfarenheter. Du driver dina projekt effektivt och med st\u00e4ndig f\u00f6rb\u00e4ttring som m\u00e5l. Du har mycket god samarbetsf\u00f6rm\u00e5ga samt integritet i din roll. Du trivs i en utvecklande milj\u00f6 d\u00e4r f\u00f6r\u00e4ndrings- och f\u00f6rb\u00e4ttringsarbete \u00e4r en del av vardagen. Du \u00e4r noggrann, strukturerad och har ett utpr\u00e4glat kvalitetsmedvetande som genomsyrar dina handlingar. Du kommer att vara en viktig del i ett mycket trevligt g\u00e4ng i en stimulerande milj\u00f6 d\u00e4r du f\u00e5r ta del av nya utvecklingsprojekt som ofta blir verklighet i form av state-of-the art l\u00e4kemedel.\u00a0\nVi ser fram emot att f\u00e5 ber\u00e4tta mer om tj\u00e4nsten och Sever Pharma Solutions! Tveka inte att h\u00f6ra av dig f\u00f6r mer information eller f\u00f6r att f\u00e5 svar p\u00e5 dina fr\u00e5gor. Vi kommer att granska ans\u00f6kningarna l\u00f6pande. Varmt v\u00e4lkommen!","price":null,"currency":"SEK","status":"active","noindex":false,"location":{"address":null,"full_address":null,"city":"Malm\u00f6","country":"SE","latitude":55.563911049712,"longitude":12.973142533039},"metadata":{"region":"Sk\u00e5ne l\u00e4n","duration":"Tills vidare","employer":"Technogarden AB","postcode":"21532","positions":1,"profession":"L\u00e4kemedelsinspekt\u00f6r","salary_type":"Fast m\u00e5nads- vecko- eller timl\u00f6n","employer_url":"https:\/\/www.severpharmasolutions.com\/","scope_of_work":"100\u2013100 %","working_hours":"Heltid","contact_person":"Carolina Pankarz Bernro","employment_type":"Vanlig anst\u00e4llning","occupation_field":"Naturvetenskap","employer_workplace":"Sever Pharma Solutions","experience_required":true},"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":"+46730981310","owner_email":"carolina.pankarz.bernro@technogarden.se","images":[],"published_at":"2026-08-17T11:31:12+00:00","expires_at":"2026-09-30T23:59:59+00:00","created_at":"2026-08-18T03:47:57+00:00","updated_at":"2026-08-19T02:45:40+00:00"}}