Join Our Team as a QA Manager We are looking for a full time Quality Assurance Manager to join and strengthen the GMP Operations team at Anocca. The GMP operations team currently consist of a production team, a QC team, QA managers including QP, facility manager, validation and project managers, for a total of 20 colleagues. You will be involved in the quality assurance of all operative activities, including document approval, deviation investigations, material release, training of employees, validation of equipment, maintenance of the Quality Management System (QMS) and validation of methods for release of ATMP products, to be used in clinical trials. Also, document administration will be an important part of this role. Prior experience of working in a GMP environment, either in close collaboration with Quality Assurance departments or within Quality Assurance, is required for this role. Experience in regulatory guidelines for ATMP (EudraLex Vol.4), aseptic work (EudraLex Annex 1) or in microbiology would be a significant asset. You must be capable of working as part of a team and as the company and team is very international and the business language is English, excellent English communication skills both in speech and in writing is required. The role is suited to motivated persons with a drive to learn and grow in a complex and varied environment. What we are looking for: • BSc or MSc in life science subject (biology, pharmacy, chemistry or similar) • Experience working according to GMP • Meticulous documentation administration skills • Experienced in deviation investigations, CC and CAPAs • Fluent written and spoken English We offer: An international workplace with plenty of variety in the job, interaction with all other Anocca employees and the opportunity to work at the exciting intersection of biotechnology and medicine. Compensation: • Monthly salary • Tier 1 occupational pension plan • Wellness grant • Flexible work hours How to Apply: If this QA position resonates with you, we would love to hear from you. Submit your application, including your CV and a cover letter, through our careers portal. Join us in making a difference, apply now! We ensure unbiased recruitment by hiding your personal information such as name, email, etc. and photos from the recruiter during the screening process.

Are you skilled in using and developing cell-based assays for antibody characterization? Do you wish to work in a well-funded, science-driven organization with highly skilled colleagues focusing on the battle against neurodegenerative disorders? Then you could be our next Scientist in the In vitro Pharmacology section, where we currently have a one-year temporary contract available. The Role You will join a collaborative and science-driven project team working on a diverse and emerging portfolio with projects in various phases from discovery through clinical development. Your focus will be the execution and development of in vitro methods, cell-based assays in particular, to support characterisation of candidates integrated with our BrainTransporter technology platform. Key responsibilities include: Characterising drug candidates for target binding, cell uptake, mechanism of action and immunotoxicity Planning and performing laboratory work with techniques such as FACS, ELISA, MSD, immunocytochemistry and microscopy Developing and optimising new methods Analysing, documenting and presenting results within project teams Contributing to method development and scientific strategy in the lab Qualifications MSc or PhD in a relevant natural science discipline Expertise in using and developing cell-based assays Experience in in vitro characterisation of drug candidates; experience with biologics (especially antibodies) is meriting Proficiency in analytical methods such as flow cytometry and plate-based immunoassays Fluent written and spoken English Meritorious: Experience with confocal or high-content microscopy Knowledge of functional assays and live cell imaging Previous work in the biopharmaceutical/biotech industry Familiarity with 2D/3D cell cultures or disease models for neurodegeneration Swedish language skills Personal Attributes We are looking for someone who is: Systematic and analytical, with a strong sense of responsibility Proactive and solution-oriented, with high ethical standards A strong communicator who enjoys working in cross-functional teams Motivated by hands-on work and continuous improvement You demonstrate and are inspired by the behaviours that reinforce BioArctic’s core values (Respect, Commitment, Collaboration and Responsibility). Contract Details Duration: 12-month parental leave cover Start date: As soon as possible/upon agreement Location: Kungsholmen, Stockholm Working hours: Full-time, 40 hours/week Application deadline: Ongoing – position open until filled How to Apply If you’re excited by this opportunity, apply as soon as possible. For any questions contact Recruitment Consultant Anna Rennermalm – (Search4S Dustgoat AB), [email protected], +46 70 794 20 05 We welcome your application! About BioArctic BioArctic is an innovative Swedish biopharma company focusing on research into neurodegenerative diseases, such as Alzheimer’s disease, Parkinson’s disease and ALS. BioArctic’s research has resulted in the world’s first fully approved disease-modifying drug against Alzheimer’s disease. The company has also developed the BrainTransporter technology, that has the possibility to improve the result of treatment against diseases of the brain. BioArctic’s head office is located in Stockholm Sweden, and the company has more than 130 employees. Learn more about the company on www.bioarctic.com

Scandinavian Biopharma är ett forskningsbaserat biotechföretag fast beslutna att hjälpa människor i hela världen till ett bättre och längre liv. De är på god väg att göra så genom utveckling av världens första vaccin mot ETEC-bakterier. ETEC infektioner kan bli svåra hos både barn och vuxna med svåra diarréer som följd. Mest utsatta är små barn som kan få bestående men och även avlida till följd av infektionen. Scandinavian Biopharma distribuerar även i främst norra Europa, ett brett sortiment av biologiska specialistläkemedel med fokus på vacciner och immunglobuliner. I dagsläget har Scandinavian Biopharma redan lovande säkerhets och skyddsdata för ETVAX från fas 2b-studien hos finska resenärer till Benin, Västafrika. Vi har vaccinerat 5 000 barn i en fas 2b-studie i Gambia och förbereder som bäst inför en effektstudie (fas 3) studie i USA och en stor effektstudie i Zambia (fas 3). SB är välfinansierade både av internationella statliga medel samt genom Scandinavian Biopharmas egna distributionsverksamhet. Tjänsten som Drug Substance Specialist Scandinavian Biopharma stärker nu upp teamet inom Manufacturing och söker en engagerad och erfaren Drug Substance Specialist som vill vara med på resan att inom kort ha ett kommersiellt tillgängligt ETEC-vaccin på marknaden. Manufacturing teamet jobbar endast med external Manufacturing och ansvarar för samarbetet med globala CMO nätverk för produktion av företagets läkemedelsprodukter. I rollen som Drug Substance Specialist har du en nyckelfunktion i arbetet med tillverkning och uppskalning av våra 6 Drug Substance komponenter som ingår i vårt ETEC vaccin som är i sen utvecklingsfas. Arbetet inkluderar Technology Transfer av tillverkning till våra kontraktstillverkare (CMO:er), koordinering av processutvecklingsarbete och säkerställa tillverkning av klinikmaterial. Rollen innehåller mycket samarbete externt med CMO:er och även internt med medarbetare inom Manufacturing, Development, Regulatory och QA avdelningarna. Huvudsakliga arbetsuppgifter: Tech Transfer. Processvalidering. Skriva och granska tillverkningsmetoder, valideringsprotokoll och annan produktionsdokumentation. Skriva rapporter för produkt och produktion av bioteknologiska substanser. Skapa goda och långsiktiga relationer med samarbetspartner CMO. Sammanställa och utvärdera resultat från produktion hos CMO. Skriva/granska regulatoriska dokument som ingår i CMC. Tillsammans med teamet på Manufacturing bidra till att produktion av Drug Substance hos CMO sker effektivt och enligt GMP. Stödja processvalidering som är utlagd på CMO, vilket kan innebära resor. Vi söker dig som trivs på ett entreprenörsdrivet bolag och i en roll som blandar praktiskt arbete med mer övergripande strategiska uppgifter. Du är noggrann, har integritet men är också prestigelös i ditt samarbetssätt samt tar ägarskap. Du samarbetar gärna tvärfunktionellt inom organisationen och drivs av att skapa resultat framåt och säkerställa bra processer för extern tillverkning.   Du erbjuds ett ansvarsfullt jobb i ett stimulerande klimat med högt i tak och blir en del av en grupp ambitiösa och duktiga medarbetare som har roligt på jobbet! Utbildning, kvalifikationer och erfarenhet: · Universitetsutbildning inom Civilingenjör bioteknik, farmacevt, Biokemi eller liknande naturvetenskaplig utbildning. · Flerårig erfarenhet av odling och rening inom läkemedelstillverkning. · Erfarenhet av arbete med CMO:er. · Erfarenhet av cGMP tillverkning av biologiska läkemedel och vacciner. · God förmåga att kommunicera i tal och skrift (engelska o svenska). Tjänsten är på heltid och rapporterar till VP Manufacturing, kontoret är placerat i Solna. Ansökan I denna rekrytering samarbetar Scandinavian Biopharma med SallyQ. Om du är intresserad av tjänsten och vill ha mer information, kontakta Ellinor Crafoord, Senior rekryteringskonsult, 079-3554257 eller [email protected]. Sista ansökningsdag: 30 april 2025, men urval och intervjuer sker löpande så vi välkomnar din ansökan redan idag. Om oss Vi är entreprenörer och experter inom global vaccinutveckling, tillverkning, registrering och kommersialisering av bioläkemedelsprodukter. Vår arbetsmiljö präglas av våra kärnvärden där lagarbete, talang, och personlig utveckling aktivt främjas. Vi är världsledande i diarrévacciner mot ETEC. På Scandinavian Biopharma är vi ett sammansvetsat team med god gemenskap och med en spännande resa framför oss – vi hoppas du vill vara med oss på denna resa!

We are looking for a full time analytical engineer to join and strengthen the QC team which consists of one scientist, one senior analytical engineer (recruitment ongoing) one analytical engineer and one process technician. The QC team is part of the larger GMP operations team consisting of a production team, QA managers, facility manager, application specialist, for a total of 20 colleagues. You will be involved in the setup, validation and execution of QC methods for the analysis and release of ATMP products, to be used in clinical trials. You will also participate in environmental monitoring sampling, raw material control, deviation investigations and review of documentation. Experience in cell culture, flow cytometry, potency assays, ddPCR, qPCR, mycoplasma, sterility and endotoxin tests would be a significant asset; particularly in the context of ATMP analysis. Knowledge of aseptic work techniques is desirable. Prior experience working in a GMP environment is preferred for the role. You must be capable of working as part of a team and as the company and team is very international and the business language is English, excellent English communication skills is required. The role is suited to motivated persons with a drive to learn and grow in a complex and varied environment. What we are looking for: • Experience working according to GMP. • Quality control experience in the cell therapy or ATMP space. • Experienced in writing deviation investigations, CC and CAPA’s. • Good grasp of the underlying biology related to cell engineering. • Experience in microbiology. • Fluent written and spoken English. We offer: An international workplace, with plenty of variety in the job, interaction with all other Anocca employees and the opportunity to work at the exciting intersection of biotechnology and medicine. Please note that we contact candidates that we would like to invite for an interview within 3 weeks after the advertisement has closed. Unsuccessful candidates will not be contacted. Compensation Monthly salary Tier 1 occupational pension plan Wellness grant Flexible work hours We ensure unbiased recruitment by hiding your personal information such as name, email, etc. and photos from the recruiter during the screening process.

Join Our Team as a Bioengineer! We are currently seeking a highly motivated Bioengineer to join our dynamic team. In your role as Bioengineer, you will play a crucial role in ensuring the efficiency and effectiveness of our processes. If you have a passion for technology and a keen eye for detail, we encourage you to apply. About the RoleWe are looking for a highly motivated Bioengineer to join our Specimen Core. You will be involved in research projects employing cutting edge technologies, and state of the art equipment. The Bioengineer role at Anocca is a junior role for graduates with a keen interest in biotechnology and life sciences. As a part of Specimen Core you will contribute to Anocca’s operations by isolation and banking of cells from blood specimens, including their genetic and phenotypic characterisation. You will also support operations with equipment maintenance and service. Being a part of our Specimen Core includes routine handling of incoming blood: PBMC isolation from blood and banking DNA extraction from cells Phenotypic analysis of cells by flow cytometry What We're Looking For: Molecular biology laboratory skills Experience in working with primary human cells Good time management skills and proficient in data documentation Fluent written and spoken English It would be nice if you have: Experience with handling blood Experience in gene-editing technologies Experience of quality system driven operations (ISO, GxP or equivalent) Why us: Our company is at the forefront of technological innovation, striving to make a difference in the industry. We offer a dynamic working environment where talent and ambition are recognized and rewarded. Join us, and be part of a team that values growth, collaboration, and the pursuit of excellence. We Offer: Competitive salary and benefits package. Opportunities for professional development and career advancement. A collaborative and supportive work culture. State-of-the-art facilities and resources. How to Apply:If this position resonates with you, we would love to hear from you. Submit your application, including your CV and a cover letter. Join us in making a difference, apply now! We ensure unbiased recruitment by hiding your personal information such as name, email, etc. and photos from the recruiter during the screening process.

Join Our Team as a Laboratory Technician! We are currently seeking highly motivated Laboratory Technician to join our dynamic team. In your role as Technician, you will play a crucial role in ensuring the efficiency and effectiveness of our processes. If you have a passion for technology and a keen eye for detail, we encourage you to apply. About the RoleWe are looking for a highly motivated Lab Tech to join our Specimen Core. You will be involved in research projects employing cutting edge technologies, and state of the art equipment. The Laboratory Technician role at Anocca is a junior role for graduates with a keen interest in biotechnology and life sciences. As a part of Specimen Core you will contribute to Anocca’s operations by isolation and banking of cells from blood specimens, including their genetic and phenotypic characterisation. You will also support operations with equipment maintenance and service. Being a part of our Specimen Core includes routine handling of incoming blood: PBMC isolation from blood and banking DNA extraction from cells Phenotyping of cells by flow cytometry What We're Looking For: Molecular biology laboratory skills Good time management skills and proficient in data documentation Fluent written and spoken English It would be nice if you have: Experience with handling blood Some experience of working with primary cells Experience of quality system driven operations (ISO, GxP or equivalent) Why us: Our company is at the forefront of technological innovation, striving to make a difference in the industry. We offer a dynamic working environment where talent and ambition are recognized and rewarded. Join us, and be part of a team that values growth, collaboration, and the pursuit of excellence. We Offer: Competitive salary and benefits package. Opportunities for professional development and career advancement. A collaborative and supportive work culture. State-of-the-art facilities and resources. How to Apply:If this position resonates with you, we would love to hear from you. Submit your application, including your CV and a cover letter. Join us in making a difference, apply now!

Job description: We are looking for a full time senior analytical engineer to join and strengthen the QC team which consists of one scientist, 2 analytical engineers and 1 process technician. The QC team is part of the larger GMP operations team consisting of a production team, QA managers, facility manager, application specialist, for a total of 20 colleagues. You will be involved in the setup, validation and execution of QC methods for the analysis and release of ATMP products, to be used in clinical trials. You will also take a leading role in deviation investigations and review of documentation. Experience of cell culture, flow cytometry, potency assays, ddPCR, qPCR, mycoplasma, sterility and endotoxin tests would be a significant asset; particularly in the context of ATMP analysis. Knowledge of aseptic manufacturing techniques is desirable. Prior experience working in a GMP environment is essential for the role. You must be capable of working as part of a team and demonstrate initiative to drive projects forward. As the company and team is very international and the business language is English, excellent English communication skills is required. The role is suited to experienced and motivated professionals with a drive to lead and execute by action. What we are looking for: • Experience working according to GMP.• Quality control experience in the cell therapy or ATMP space.• Significant and relevant experience in instrument and method validation.• Experienced in writing and leading deviation investigations, CC and CAPA’s.• Good grasp of the underlying biology related to cell engineering.• Experience in microbiology.• Fluent written and spoken English. We offer: An international workplace, with plenty of variety in the job, interaction with all other Anocca employees and the opportunity to work at the exciting intersection of biotechnology and medicine. Please note that we contact candidates that we would like to invite for an interview within 3 weeks after the advertisement has closed. Unsuccessful candidates will not be contacted.Compensation Monthly salaryTier 1 occupational pension planWellness grantFlexible work hours When to apply:Last day to apply 2025-03-31EmployerAnocca AB(org.nr 556946-2384)