{"data":{"id":182874,"slug":"gmp-ansvarig-farmaceut-extempore-3d-printing","type":"job","title":"GMP-Responsible Pharmacist \u2013 Extemporaneous Preparation & 3D Printing","description":"AtrimusRx is seeking an experienced pharmacist with strong expertise in GMP and extemporaneous manufacturing who is ready to take GMP responsibility for our 3D printing operations focused on individually tailored medications.\nThis is a central role for someone with a solid pharmaceutical and quality foundation, who is also driven by development and the opportunity to make a tangible difference for patients.\nWe're looking for someone who is curious, enjoys solving complex problems, and gets energized \u2013 maybe even a little excited \u2013 when facing a new challenge.\nAt AtrimusRx, pharmaceutical quality, technology, and development come together \u2013 with the patient's needs as our starting point.\nWhy do we work with 3D printing of medications?\nNot all patients fit into the doses and formulations that are commercially available. This is especially true for children, where medication needs and dosing can look very different than for adults.\nIn practice, this can mean that tablets need to be divided or crushed, or that capsule contents need to be mixed with food or drink for a child to receive their prescribed treatment.\nWe believe there should be better options.\nWith 3D printing of individually tailored medications, we work to be able to manufacture medications in a dose, strength, and formulation adapted to each individual patient's needs from the start. The goal is to reduce the need to manipulate medications after the fact that were not originally designed for the patient.\nFor us, 3D printing is therefore not about the technology itself. The technology is a tool to solve a real problem for patients, families, and healthcare providers.\nThis is the operation you will help quality assure and develop.\nAbout the role\nAs GMP-responsible pharmacist, you will have a central function in our extemporaneous operations. You will work closely with our operational manufacturing and our pharmacists and are responsible for developing and maintaining robust quality work as the operations grow and evolve.\nYour work tasks include:\nresponsibility for and further development of GMP work within the operation\nensuring that processes, manufacturing, and documentation meet applicable quality and regulatory requirements\nresponsibility for deviation management, CAPA, change control, and risk assessments\ndriving and following up on qualification and validation of equipment, processes, and manufacturing methods\ndeveloping, reviewing, and implementing SOPs, instructions, and other governing documentation\nensuring structured and continuous quality work\ncontributing quality expertise in the development and implementation of new substances, formulations, and manufacturing processes\nassisting with regulatory inspections and regulatory quality matters\ncontinuously identifying and driving improvements in processes, work methods, and quality systems\n\nWe are looking for someone who\nis a licensed pharmacist or pharmaceutical technician and has:\ndocumented previous experience with GMP responsibility\nsolid practical experience working according to GMP\nexperience with extemporaneous manufacturing\ngood experience with pharmaceutical quality systems and GMP documentation\nexperience with deviation management, CAPA, change control, and risk management\nexperience with qualification and validation\ngood ability to interpret regulatory requirements and translate them into practical and well-functioning processes\n\nPrevious experience with 3D printing is not a requirement. What matters is that you have the right pharmaceutical and GMP expertise, as well as the curiosity and willingness to learn and develop in a new area.\nAs a person\nYou are curious, solution-oriented, and have a genuine interest in development.\nYou enjoy deepening your knowledge and understanding complex issues. When you encounter a problem, your natural approach is to explore the possibilities, analyze alternatives, and find a well-grounded path forward.\nWe value people who dare to ask questions, think in new ways, and challenge established methods when there are factual reasons to do so. At the same time, you have the thoroughness, integrity, and respect for quality and regulations that are required to bear GMP responsibility.\nFor us, curiosity and the desire to continue learning are important qualities. We believe you will thrive best with us if new challenges spark engagement rather than hesitation, and if you appreciate solving complex problems together with others.\nAnd perhaps most importantly: you understand that quality systems, processes, and documentation ultimately exist for a reason \u2013 for the patient.\nAbout AtrimusRx\nAtrimusRx works with complex aspects of pharmaceutical supply, including drug shortages, licensed medicines, pharmaceutical distribution, and extemporaneous manufacturing.\nAtrimusRx is Sweden's first open-care pharmacy that extemporaneously manufactures medications from the beginning, from APIs. Within our extemporaneous operations, we work with 3D printing of individually tailored medications to enable doses, strengths, and formulations adapted to the patient's needs.\nThis is particularly significant for children, where available medications are not always adapted to their needs and tablets therefore may need to be divided or crushed or capsule contents mixed with food. Our ambition is for the medication to be manufactured from the start based on the patient's prescribed dose and needs.\nWe are a specialist-driven and entrepreneurial organization where innovation and quality go hand in hand, with patient safety as the obvious starting point.\nAs GMP-responsible pharmacist, you will become an important part of the work to develop individually tailored pharmaceutical manufacturing that can make a real difference for patients.\nTerms of Employment\nFull-time employment, 40 hours per week.\nFixed hours 08:00\u201317:00.\nThe position is located at AtrimusRx in Sollentuna.\nRemote work is not applicable as the role involves on-site work in our pharmacy and manufacturing operations.\n\nApplication Process\nThe recruitment process begins with two tests:\nPersonality test \u2013 takes approximately 2 minutes.\nCognitive test \u2013 takes approximately 12 minutes and 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.\nMeticulousness, attention to detail, and the ability to follow instructions are critical qualities for this position. The application process therefore forms part of our initial screening.\nSelection and interviews take place on an ongoing basis and the position may be filled before the final application deadline.\nWe decline contact from media sales representatives, recruitment consultants, and other providers of recruitment and advertising services.","language":"sv","is_translated":true,"title_original":"GMP-ansvarig farmaceut \u2013 Extempore & 3D-printing","description_original":"AtrimusRx s\u00f6ker en erfaren farmaceut med gedigen kompetens inom GMP och extemporetillverkning som vill ta GMP-ansvar f\u00f6r v\u00e5r verksamhet inom 3D-printing av individanpassade l\u00e4kemedel.\nDet h\u00e4r \u00e4r en central roll f\u00f6r dig som har en stark farmaceutisk och kvalitetsm\u00e4ssig grund, men som ocks\u00e5 drivs av utveckling och av m\u00f6jligheten att g\u00f6ra konkret skillnad f\u00f6r patienter.\nVi s\u00f6ker dig som \u00e4r nyfiken, tycker om att l\u00f6sa komplexa problem och f\u00e5r lite extra energi \u2013 kanske till och med pirr i magen \u2013 n\u00e4r du st\u00e4lls inf\u00f6r en ny utmaning.\nHos oss m\u00f6ts farmaceutisk kvalitet, teknologi och utveckling \u2013 med patientens behov som utg\u00e5ngspunkt.\nVarf\u00f6r arbetar vi med 3D-printing av l\u00e4kemedel?\nAlla patienter passar inte in i de doser och beredningsformer som finns kommersiellt tillg\u00e4ngliga. Det g\u00e4ller inte minst barn, d\u00e4r behovet av l\u00e4kemedel och dosering kan se helt annorlunda ut \u00e4n f\u00f6r vuxna.\nI praktiken kan det inneb\u00e4ra att tabletter beh\u00f6ver delas eller krossas, eller att inneh\u00e5llet i kapslar beh\u00f6ver blandas med mat eller dryck f\u00f6r att ett barn ska kunna f\u00e5 sin ordinerade behandling.\nVi tycker att det ska finnas b\u00e4ttre m\u00f6jligheter.\nMed 3D-printing av individanpassade l\u00e4kemedel arbetar vi f\u00f6r att kunna tillverka l\u00e4kemedel i en dos, styrka och beredningsform som \u00e4r anpassad efter den enskilda patientens behov fr\u00e5n b\u00f6rjan. M\u00e5let \u00e4r att minska behovet av att i efterhand manipulera l\u00e4kemedel som ursprungligen inte har utformats f\u00f6r patienten.\nF\u00f6r oss handlar 3D-printing d\u00e4rf\u00f6r inte om tekniken i sig. Tekniken \u00e4r ett verktyg f\u00f6r att l\u00f6sa ett verkligt problem f\u00f6r patienter, n\u00e4rst\u00e5ende och v\u00e5rden.\nDet \u00e4r den verksamheten du kommer att vara med och kvalitetss\u00e4kra och utveckla.\nOm rollen\nSom GMP-ansvarig f\u00e5r du en central funktion i v\u00e5r extemporeverksamhet. Du arbetar n\u00e4ra den operativa tillverkningen och v\u00e5ra farmaceuter och ansvarar f\u00f6r att utveckla och uppr\u00e4tth\u00e5lla ett robust kvalitetsarbete i takt med att verksamheten v\u00e4xer och utvecklas.\nDina arbetsuppgifter omfattar bland annat att:\nansvara f\u00f6r och vidareutveckla GMP-arbetet inom verksamheten\ns\u00e4kerst\u00e4lla att processer, tillverkning och dokumentation uppfyller g\u00e4llande kvalitets- och regulatoriska krav\nansvara f\u00f6r avvikelsehantering, CAPA, change control och riskbed\u00f6mningar\ndriva och f\u00f6lja upp kvalificering och validering av utrustning, processer och tillverkningsmetoder\nutveckla, granska och implementera SOP, instruktioner och annan styrande dokumentation\ns\u00e4kerst\u00e4lla ett strukturerat och kontinuerligt kvalitetsarbete\nbidra med kvalitetskompetens vid utveckling och implementering av nya substanser, beredningsformer och tillverkningsprocesser\nbidra vid myndighetsinspektioner och i regulatoriska kvalitetsfr\u00e5gor\nkontinuerligt identifiera och driva f\u00f6rb\u00e4ttringar av processer, arbetss\u00e4tt och kvalitetssystem\n\nVi s\u00f6ker dig som\n\u00e4r legitimerad apotekare eller receptarie och har:\ndokumenterad tidigare erfarenhet av GMP-ansvar\ngedigen praktisk erfarenhet av arbete enligt GMP\nerfarenhet av extemporetillverkning\ngod erfarenhet av farmaceutiska kvalitetssystem och GMP-dokumentation\nerfarenhet av avvikelsehantering, CAPA, change control och riskhantering\nerfarenhet av kvalificering och validering\ngod f\u00f6rm\u00e5ga att tolka regulatoriska krav och oms\u00e4tta dem i praktiska och v\u00e4lfungerande processer\n\nTidigare erfarenhet av 3D-printing \u00e4r inte ett krav. Det viktiga \u00e4r att du har r\u00e4tt farmaceutisk och GMP-m\u00e4ssig kompetens samt nyfikenheten och viljan att l\u00e4ra dig och utvecklas inom ett nytt omr\u00e5de.\nSom person\nDu \u00e4r nyfiken, l\u00f6sningsorienterad och har ett genuint intresse f\u00f6r utveckling.\nDu tycker om att f\u00f6rdjupa din kunskap och f\u00f6rst\u00e5 komplexa fr\u00e5gest\u00e4llningar. N\u00e4r du m\u00f6ter ett problem \u00e4r din naturliga inst\u00e4llning att unders\u00f6ka m\u00f6jligheterna, analysera alternativen och hitta en v\u00e4lgrundad v\u00e4g fram\u00e5t.\nVi uppskattar personer som v\u00e5gar st\u00e4lla fr\u00e5gor, t\u00e4nka i nya banor och utmana etablerade arbetss\u00e4tt n\u00e4r det finns sakliga sk\u00e4l f\u00f6r det. Samtidigt har du den noggrannhet, integritet och respekt f\u00f6r kvalitet och regelverk som kr\u00e4vs f\u00f6r att b\u00e4ra ett GMP-ansvar.\nF\u00f6r oss \u00e4r nyfikenhet och viljan att forts\u00e4tta l\u00e4ra sig viktiga egenskaper. Vi tror att du trivs b\u00e4st hos oss om nya utmaningar v\u00e4cker engagemang snarare \u00e4n tvekan och om du uppskattar att tillsammans med andra l\u00f6sa komplexa problem.\nOch kanske viktigast av allt: du f\u00f6rst\u00e5r att kvalitetssystem, processer och dokumentation ytterst finns av en anledning \u2013 f\u00f6r patienten.\nOm AtrimusRx\nAtrimusRx arbetar med komplexa delar av l\u00e4kemedelsf\u00f6rs\u00f6rjningen, bland annat l\u00e4kemedelsbrist, licensl\u00e4kemedel, l\u00e4kemedelsdistribution och extemporetillverkning.\nAtrimusRx \u00e4r Sveriges f\u00f6rsta \u00f6ppenv\u00e5rdsapotek som extemporetillverkar l\u00e4kemedel fr\u00e5n grunden, API. Inom v\u00e5r extemporeverksamhet arbetar vi med 3D-printing av individanpassade l\u00e4kemedel f\u00f6r att m\u00f6jligg\u00f6ra doser, styrkor och beredningsformer anpassade efter patientens behov.\nDet \u00e4r s\u00e4rskilt betydelsefullt f\u00f6r barn, d\u00e4r tillg\u00e4ngliga l\u00e4kemedel inte alltid \u00e4r anpassade efter deras behov och tabletter d\u00e4rf\u00f6r kan beh\u00f6va delas eller krossas eller kapselinneh\u00e5ll blandas med f\u00f6da. V\u00e5r ambition \u00e4r att l\u00e4kemedlet redan fr\u00e5n b\u00f6rjan ska kunna tillverkas utifr\u00e5n patientens ordinerade dos och behov.\nVi \u00e4r en specialistdriven och entrepren\u00f6riell organisation d\u00e4r innovation och kvalitet g\u00e5r hand i hand, med patients\u00e4kerheten som sj\u00e4lvklar utg\u00e5ngspunkt.\nSom GMP-ansvarig blir du en viktig del i arbetet med att utveckla individanpassad l\u00e4kemedelstillverkning som kan g\u00f6ra verklig skillnad f\u00f6r patienter.\nAnst\u00e4llningsvillkor\nHeltidsanst\u00e4llning, 40 timmar per vecka.\nFast arbetstid kl. 08.00\u201317.00.\nTj\u00e4nsten \u00e4r placerad p\u00e5 AtrimusRx i Sollentuna.\nDistansarbete \u00e4r inte aktuellt eftersom rollen omfattar arbete p\u00e5 plats i v\u00e5r apoteks- och tillverkningsverksamhet.\n\nAns\u00f6kningsf\u00f6rfarande\nRekryteringsprocessen inleds med tv\u00e5 tester:\nPersonlighetstest \u2013 tar cirka 2 minuter.\nKognitivt test \u2013 tar cirka 12 minuter och 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 och tj\u00e4nsten kan komma att tills\u00e4ttas f\u00f6re sista ans\u00f6kningsdag.\nVi undanber oss kontakt fr\u00e5n medias\u00e4ljare, rekryteringskonsulter och andra leverant\u00f6rer av rekryterings- och annonseringstj\u00e4nster.","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":"Apotekare","salary_type":"Fast m\u00e5nads- vecko- eller timl\u00f6n","employer_url":"https:\/\/atrimusrx.com\/","scope_of_work":"100\u2013100 %","working_hours":"Heltid","employment_type":"full_time","occupation_field":"H\u00e4lso- och sjukv\u00e5rd","employer_workplace":"Atrimusrx AB","translation_status":"done","experience_required":true,"employment_type_label":"Tillsvidareanst\u00e4llning (inkl. eventuell provanst\u00e4llning)"},"user_id":null,"is_sponsored":false,"views_count":0,"ai_views_count":2,"ai_vendor_counts":{"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":"2026-09-01T16:35:20+00:00","expires_at":"2026-10-01T23:59:59+00:00","created_at":"2026-09-02T03:18:09+00:00","updated_at":"2026-09-02T04:01:34+00:00"}}