Sökresultat för "Pharmaceutical R&D"

Vill du arbeta nära forskning och utveckling av framtidens läkemedelsprodukter? Vi söker nu en analytisk kemist eller laboratorietekniker som vill bidra med sin kompetens inom provupparbetning och HPLC-analys och vara en viktig del av vårt utvecklingsteam. I rollen arbetar du med att säkerställa högkvalitativ och tillförlitlig analysdata genom provberedning, haltbestämningar, upplösningsförsök och impurityanalyser. Du kombinerar praktiskt laboratoriearbete med datagranskning, dokumentation och samarbete med kollegor inom analys, formulering och projektledning. Hos oss får du arbeta i en utvecklingsmiljö där dina analyser bidrar till viktiga beslut i prekliniska och tidiga kliniska projekt. Rollen passar dig som trivs i laboratoriet, uppskattar noggrant och strukturerat arbete och samtidigt vill bidra till att utveckla arbetssätt, kvalitet och processer. Exempel på arbetsuppgifter Du kommer bland annat att: Utföra provupparbetning inför analytiska körningar, inklusive haltbestämningar, upplösningsförsök och impurityanalyser. Genomföra HPLC-UV-analyser enligt etablerade metoder och protokoll. Granska och bedöma analysresultat samt uppmärksamma och rapportera avvikelser eller oväntade resultat. Förbereda mobilfaser, buffertar och reagens för laboratoriearbetet. Delta i planering, genomförande och dokumentation av experiment och studier. Granska data och säkerställa att analyser genomförs enligt gällande kvalitetskrav. Bidra till stabilitetsstudier och tvärfunktionella utvecklingsprojekt. Delta i den dagliga driften av laboratoriet, inklusive instrumentvård och enklare underhåll av HPLC-utrustning. Vi söker dig som gillar att kombinera noggrannhet och struktur med nyfikenhet och problemlösning. Du trivs med laborativt arbete och har ett naturligt fokus på kvalitet i allt du gör. Samtidigt tycker du om att samarbeta med andra, dela kunskap och bidra till att utveckla både metoder och arbetssätt. Oavsett om det handlar om rutinmässiga analyser eller nya utmaningar drivs du av att leverera tillförlitliga resultat som bidrar till att föra projekten framåt. För rollen ser vi också att du: Har en akademisk utbildning inom analytisk kemi, fysikalisk kemi, materialkemi, farmaceutisk vetenskap eller motsvarande. Har erfarenhet av analytiskt laborativt arbete, gärna med HPLC eller andra kromatografiska tekniker. Har mycket goda kunskaper i engelska och kan kommunicera väl i både tal och skrift. Har goda kunskaper i svenska. Det är meriterande om du har Erfarenhet från GMP-reglerad verksamhet eller andra kvalitetssystem. Vana att arbeta enligt etablerade analysmetoder och instruktioner. Erfarenhet av kromatografimjukvaran Chromeleon. Erfarenhet av provupparbetning, HPLC-UV eller närliggande analystekniker. Om Nanexa Nanexa är ett innovativt läkemedelsbolag med bas i Uppsala som utvecklar framtidens depåläkemedel. Genom vår unika PharmaShell®-teknologi kombinerar vi avancerad materialvetenskap med läkemedelsutveckling för att skapa nya behandlingsmöjligheter inom flera terapiområden. Hos oss blir du en del av ett engagerat team där vetenskaplig nyfikenhet, kvalitet och samarbete driver utvecklingen framåt. Vår kultur På Nanexa bygger vi vår kultur på tre värderingar – att vara stöttande, målinriktade och kreativa. För oss innebär det att vi hjälper varandra att lyckas, arbetar fokuserat mot gemensamma mål och vågar tänka nytt för att hitta lösningar på komplexa utmaningar. Vi kombinerar vetenskaplig noggrannhet med nyfikenhet och entreprenörsanda, och tror att de bästa resultaten skapas när människor samarbetar, delar kunskap och utvecklas tillsammans. Ansökan Låter detta som en roll för dig? Varmt välkommen med din ansökan på rekrytering@nanexa.se senast den 30/8. Märk din ansökan med HPLC. Urval och intervjuer sker löpande, så skicka gärna in din ansökan så snart som möjligt. Har du frågor om tjänsten är du välkommen att kontakta Joel Hellrup, Head of Pharmaceutical R&D, på +46 (0) 70 972 27 45 eller joel.hellrup@nanexa.se. För frågor om rekryteringsprocessen är du välkommen att kontakta Therese Näs, HR, på Therese.nas@Nanexa.se Läs gärna mer om Nanexa på vår webbplats www.nanexa.se

Vill du arbeta nära forskning och utveckling av framtidens läkemedelsprodukter? Vi söker nu en analytisk kemist eller laboratorietekniker som vill bidra med sin kompetens inom fysikalisk karakterisering och vara en viktig del av vårt utvecklingsteam. I rollen arbetar du med att analysera och förstå fysikaliska och kemiska egenskaper hos pulver, suspensioner och injicerbara formuleringar. Du kombinerar praktiskt laboratoriearbete med metodutveckling, datagranskning och samarbete med kollegor inom formulering, analys och projektledning. Hos oss får du arbeta i en utvecklingsmiljö där dina analyser bidrar till viktiga beslut i prekliniska och tidiga kliniska projekt. Rollen passar dig som trivs i laboratoriet, uppskattar noggrant och strukturerat arbete och samtidigt vill vara med och utveckla metoder, arbetssätt och processer. Exempel på arbetsuppgifter Du kommer bland annat att: Utföra fysikalisk och kemisk karakterisering av råvaror, mellanprodukter och färdiga formuleringar. Arbeta med tekniker såsom laserdiffraktion, BET, Karl Fischer, elektronmikroskopi, viskositetsmätning, TGA och HPLC. Delta i metodutveckling, metodvalidering och förbättringsarbete. Planera, genomföra och dokumentera experiment samt sammanställa resultat i rapporter. Granska data och säkerställa att analyser genomförs enligt gällande kvalitetskrav. Bidra till stabilitetsstudier och tvärfunktionella utvecklingsprojekt. Delta i den dagliga driften av laboratoriet, inklusive instrumentvård och underhåll. Vi söker dig som gillar att kombinera noggrannhet och struktur med nyfikenhet och problemlösning. Du trivs med laborativt arbete och har ett naturligt fokus på kvalitet i allt du gör. Samtidigt tycker du om att samarbeta med andra, dela kunskap och bidra till att utveckla både metoder och arbetssätt. Oavsett om det handlar om rutinmässiga analyser eller nya utmaningar drivs du av att leverera tillförlitliga resultat som bidrar till att föra projekten framåt. För rollen ser vi också att du: Har en akademisk utbildning inom analytisk kemi, fysikalisk kemi, materialkemi, farmaceutisk vetenskap eller motsvarande. Har erfarenhet av laborativt analytiskt arbete. Har mycket goda kunskaper i engelska och kan kommunicera väl i både tal och skrift. Har goda kunskaper i svenska. Det är även meriterande om du har Erfarenhet av fysikalisk karakterisering. Vana att arbeta enligt etablerade analysmetoder och instruktioner. Erfarenhet från GMP-reglerad verksamhet eller andra kvalitetssystem. Praktisk erfarenhet av flera av de analystekniker som används i rollen. Om Nanexa Nanexa är ett innovativt läkemedelsbolag med bas i Uppsala som utvecklar framtidens depåläkemedel. Genom vår unika PharmaShell®-teknologi kombinerar vi avancerad materialvetenskap med läkemedelsutveckling för att skapa nya behandlingsmöjligheter inom flera terapiområden. Hos oss blir du en del av ett engagerat team där vetenskaplig nyfikenhet, kvalitet och samarbete driver utvecklingen framåt. Vår kultur På Nanexa bygger vi vår kultur på tre värderingar – att vara stöttande, målinriktade och kreativa. För oss innebär det att vi hjälper varandra att lyckas, arbetar fokuserat mot gemensamma mål och vågar tänka nytt för att hitta lösningar på komplexa utmaningar. Vi kombinerar vetenskaplig noggrannhet med nyfikenhet och entreprenörsanda, och tror att de bästa resultaten skapas när människor samarbetar, delar kunskap och utvecklas tillsammans. Ansökan Låter detta som en roll för dig? Varmt välkommen med din ansökan på rekrytering@nanexa.se senast den 30/8. Märk din ansökan med Fysikalisk. Urval och intervjuer sker löpande, så skicka gärna in din ansökan så snart som möjligt. Har du frågor om tjänsten är du välkommen att kontakta Joel Hellrup, Head of Pharmaceutical R&D, på +46 (0) 70 972 27 45 eller joel.hellrup@nanexa.se. För frågor om rekryteringsprocessen är du välkommen att kontakta Therese Näs, HR, på Therese.nas@Nanexa.se Läs gärna mer om Nanexa på vår hemsida www.nanexa.se

Lab Manager R&D & Operations · Uppsala About the role At Navinci, we are passionate about understanding biology and disease at a deeper level. We develop technologies and applications that help researchers study proteins, signaling pathways, cellular biology, and molecular mechanisms directly in biological samples. Our work spans tissue and cell-based systems and increasingly combines information from multiple technologies and data types to generate richer biological insight. We collaborate with leading academic groups, biotech companies, and pharmaceutical partners worldwide to advance research and translational science. We are now looking for an experienced and hands-on Lab Manager to take overall responsibility for our laboratories, infrastructure, equipment, and operational support functions. This is a senior role with broad responsibility across laboratory operations, safety, facilities, equipment, and support for both R&D and production activities. Success in this role requires someone who enjoys combining strategic with practical laboratory work. You will be an important part of keeping our laboratories running efficiently while actively contributing to daily operations. What you will doLaboratory Operations & Facilities Maintain a well-organized, safe, and efficient laboratory environment Develop, implement, and maintain laboratory SOPs, instructions, and operational procedures Coordinate facility maintenance, service agreements, and landlord relations Oversee cleaning services and support infrastructure improvements Ensure laboratory resources are available to support R&D activities Environment, Health & Safety (EHS) Lead and drive continuous EHS improvements across the organization Ensure compliance with laboratory safety standards, biosafety requirements, and regulatory obligations Manage REACH and CLP related activities Create and maintain Safety Data Sheets (SDS) Act as the primary contact for inspections Conduct safety inspections and follow up on corrective actions Equipment Management Ensure laboratory equipment is maintained, serviced, calibrated, and operating effectively Coordinate external service providers and maintenance activities Maintain equipment records, service logs, and calibration schedules Evaluate and implement new equipment and laboratory tools when needed Inventory & Procurement Manage inventory of reagents, consumables, and laboratory supplies Develop and maintain efficient stock management systems Coordinate purchasing and supplier relationships Ensure uninterrupted laboratory workflows while optimizing costs Laboratory Support Support scientists and production personnel with laboratory operations Assist with laboratory setup, optimization, and workflow improvements Coordinate laboratory resources to support project priorities and production timelines Act as a key point of contact for laboratory-related questions and operational support Cell Culture & Tissue Sectioning Take overall responsibility for cell culture laboratory functionality and equipment Propagate and maintain mammalian cell lines Produce and QC slides and materials for R&D and quality control activities Oversee tissue sectioning workflows and quality standards Ensure reproducibility, training, and continuous improvement of sectioning procedures Training & Leadership Train and onboard new employees in laboratory procedures, equipment usage, and safety practices Promote a culture of quality, safety, accountability, and continuous improvement Coordinate laboratory responsibilities and ensure compliance with established procedures Must-have qualifications MSc in Biotechnology, Molecular Biology, Biochemistry, Life Science, or a related field (we also accept PhDs) Several years of laboratory experience in an industrial, academic, or healthcare setting Hands-on experience working in laboratory operations and support functions Experience with mammalian cell culture Experience with laboratory safety systems Experience managing laboratory equipment, maintenance, and service providers Strong organizational and project coordination skills Fluent in English, written and spoken Experience in most of the following areas Laboratory facility management Tissue sectioning and sample preparation Laboratory documentation Procurement and supplier management Scientific equipment qualification, maintenance, and calibration Change management and operational improvement projects Supporting both R&D and production environments Who you are Structured, organized, and dependable Hands-on and comfortable working in the laboratory on a daily basis Proactive and solution-oriented An excellent communicator who enjoys working with different functions across the company Comfortable balancing long-term planning with operational execution Driven to create efficient processes Flexible and willing to support the team where needed Motivated by enabling others to do great science Location: Uppsala, Sweden Department: R&D Employment type: Full-time

About the role At Navinci, we are passionate about understanding biology and disease at a deeper level. We develop technologies and applications that help researchers study proteins, signaling pathways, cellular biology, and molecular mechanisms directly in biological samples. Our work spans tissue and cell-based systems and increasingly combines information from multiple technologies and data types to generate richer biological insight. We collaborate with leading academic groups, biotech companies, and pharmaceutical partners worldwide to advance research and translational science. As we continue to grow, we are looking for 2–3 scientists with different backgrounds and expertise to join our R&D team. We are interested in people who are excited by science, enjoy solving complex problems, and want to contribute to the development of innovative research tools and technologies. Whether your background is in cell biology, tissue biology, spatial biology, immunology, biomarker research, assay development, translational science, omics technologies, or technology development, we would love to hear from you. What you will do Design, execute, optimize, and troubleshoot biological assays and laboratory experiments Analyze and interpret data, generate robust and reproducible results, and communicate clear conclusions Document experimental work according to quality standards and contribute to scientific decision-making Collaborate across R&D, Operations, and Commercial teams Support development of new applications, products, technologies, and improved ways of working Must-have qualifications MSc or PhD in Biotechnology, Molecular Biology, Cell Biology, Biochemistry, Immunology, Medical Science, or a related field Hands-on experience with immunofluorescence, immunohistochemistry (IHC), and other in situ staining and detection methods Experience working with both tissue samples and cell-based models Experience designing, executing, and troubleshooting biological experiments Strong skills in data analysis and presentation, experimental planning, and scientific documentation Fluent in English, written and spoken Experience in one or more of the following areas Cell culture and primary cell models RNA-based methods, transcriptomics, or other omics technologies Flow cytometry Multiplex imaging, microscopy, image analysis, or digital pathology Protein biomarker analysis and antibody-based assays Assay, application, or product development Translational research, biomarker discovery, or disease biology (e.g., oncology, immunology, neuroscience) Statistical analysis, automation, quality systems Industrial R&D, scientific publications, grant writing or patent-related activities Who you are Curious, innovative, and eager to solve scientific challenges Agile and adaptable, with the ability to work in a fast-moving environment Structured, organized, and committed to high scientific quality Hands-on, proactive, and solution-oriented Collaborative, supportive, and comfortable taking ownership of your work

At ABB, we help industries run leaner and cleaner—and every person here makes that happen. You’ll be empowered to lead, supported to grow, and proud of the impact we create together. Join us and help run what runs the world. This position reports to: Global R&D/Technology Manager Your role and responsibilities As R&D Manager, you will lead, coach, and develop three teams with mixed competencies while driving innovation and supporting the development of ABB’s next generation of DCS solutions. In this role, you will have the opportunity to lead a team of Research and Development (R&D) employees and support them in achieving agreed R&D targets. Each day, you will coach and develop the team. You will also leverage your expertise to support the management of technologies, platforms, and intellectual property. You will be part of the Control Safety and Integration area within ABB’s global DCS organization and collaborate closely with teams across R&D, product development, and global business lines. Based in Malmö, you will work in a global environment where reliability, safety, and innovation are at the core of everything we do. You will be mainly accountable for: Full responsibility for personnel, including but not limited to recruitment, allocation of work, skills development, and salary setting. Planning and maintaining an appropriate project portfolio for the team. Developing and securing the future competencies needed for next-generation products and systems. Supporting the organization in ongoing change initiatives—not necessarily driving the change, but enabling and strengthening it through strong leadership and collaboration. Ensuring the team remains receptive to the broader organization and aligned with ABB’s long‑term technology roadmap. Qualifications for the role You hold a Bachelor’s or Master’s degree in software development or the equivalent and have a strong technical background. You bring solid leadership experience, preferably as a line manager in a global organization. You have extensive experience in R&D and product development, ideally within a technology-driven environment. You possess strong communication skills and enjoy working with people — coaching, developing, and growing teams is a natural part of your leadership style. You are innovative, collaborative, and comfortable navigating a dynamic environment with both internal and external stakeholders. Experience in industrial automation and functional safety development is an asset. You communicate fluently in English and Swedish. More about ABB We develop today’s and tomorrow’s world‑leading Distributed Control Systems (DCS) for process industries across the globe. Our customers include pharmaceutical companies, mines, refineries, steel mills, and power plants — industries where reliability and safety are essential. In this role, you will contribute to shaping the next generation of DCS products and safety solutions, working closely with R&D teams who use advanced simulation tools, multi‑physics models, and cutting‑edge development methods to ensure performance, safety, and innovation. Recruiting Manager Michael Gienke, +49 172 5231495, will answer your questions about the position. Union representatives: Sveriges Ingenjörer – Peter Medin, +46 703 904 170 Ledarna – Leif Öhrberg, +46 724 64 40 16 Unionen – Mikael Hammar, +46 730 887 060. For other questions, please contact Talent Partner Irma Leijon, +46 72 461 23 14. Building a cleaner, smarter future takes all kinds of minds: the curious, the courageous, and the creative. That's why we welcome people from all backgrounds and experiences. Ready to make an impact? Apply today or visit https://www.abb.com to learn more about the impact of our solutions across the globe.

We are looking for a driven Line Controller / Business Controller with around 5 years of experience to join an international biopharmaceutical company experiencing strong growth. This is a perfect opportunity for a controller who is ready for a natural next step in their career, combining hands-on line controlling with finance business partnering in a complex global organization. We review applications continuously, so do not hesitate to apply today! About the role Our client is looking for a dedicated Line Controller to take on a central and business-facing role within Research, Development and Medical Affairs (RDMA). The organization manages an annual budget of several billion SEK, divided between project activities and the ongoing line organization, comprising approximately 200 employees and 100 cost centers across Europe, the US, and Japan. In this role, you will act as a financial business partner to several functional line leaders, translating business plans into financial realities and creating transparency around performance. This is a dynamic role suited for someone who wants to combine qualified finance business partnering with clear operational line responsibility (budgeting, forecasting, cost center management, and variance analysis) in a global environment. You are offered A natural career step: A role where you get full ownership of your areas and room to grow in a global biopharmaceutical environment. A strong international network: Collaborate closely with global functional leaders, international co-controllers, and an experienced finance team. Strategic and operational variety: A highly varied role where you move seamlessly between forecasting discussions with functional leaders and hands-on Excel analysis, cost center management, and follow-ups Work tasks Your responsibilities will include: Act as a financial business partner to functional leaders and senior stakeholders within RDMA. Develop a thorough understanding of business plans, priorities, resource requirements, and cost drivers. Constructively challenge budget owners' assumptions and plans, helping to identify practical solutions that balance scientific needs with available resources. Drive the four annual planning and forecasting cycles, including the budget process. Coordinate and quality-assure financial input from a large number of cost centers and business areas. Monitor actual performance against budget/forecast and analyze the underlying causes of variances. Identify financial risks and opportunities, explaining their impact on the full-year forecast. Take ownership of relevant month-end and quarter-end close activities (accruals, reallocations, and closing documentation). Collaborate with accounting, Business Controllers, System Controllers, and the wider global finance organization to improve processes and transparency. We are looking for Around 4-6 years of relevant experience in Business Controlling, Line Controlling, or Finance Business Partnering. Experience with budgeting, forecasting, financial planning, and performance management. Have a solid understanding of month-end closing, accruals, and other accounting-related controlling activities. Have strong analytical capabilities and advanced Excel skills. Are fluent in English and have good communication skills in Swedish. It is meritorious if you have Are fluent in Swedish. Experience in the life science pharmaceutical, research, or other knowledge-intensive industries. Experience in R&D controlling. Experience in providing financial support and guidance to teams or organizations working with clinical studies. Experience with large ERP systems, financial reporting tools, or digital/AI-enabled automation in finance. To succeed in the role, your personal skills are: Structured Proactive Driven Communicative team payer Social Our recruitment process This recruitment process is handled by Academic Work and it is our client’s wish that all questions regarding the position is directed to Academic Work. Our selection process is continuous and the advert may close before the recruitment process is completed if we have moved forward to the next phase. The process includes two tests: one personality test and one cognitive test. The tests are tools to find the right talent for the right position, to enable equality, diversity, and a fair process.

Join us as a Global Study Associate Director (GSAD) in our BioPharmaceuticals Clinical Operations team at AstraZeneca's dynamic R&D site in Gothenburg (Sweden). This role is pivotal in the delivery of clinical studies, providing direction and guidance to a cross-functional study team within the Cardiovascular, Renal and Metabolism (CVRM) therapy area. As the main liaison between the study team and the Clinical Program Team (CPT), you will be accountable for the delivery of a study according to agreed timelines, budget, and quality standards. Accountabilities As a GSAD, you will lead and provide guidance to a cross-functional study team, ensuring the clinical study progresses as planned. You will be responsible for developing essential study level documents, overseeing external service providers, and ensuring all systems used at a study-level are current and accurate. You will also oversee study level performance against agreed upon plans, milestones, and key performance indicators. Additionally, you will be responsible for study budget re-forecasting and management throughout the study lifecycle. Essential Skills/Experience University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research Relevant clinical experience in the pharmaceutical industry, including project management experience Extensive study management experience Extensive knowledge of ICH-GCP, clinical research regulatory requirements Demonstrated solid project management skills Strong abilities in team leadership with experience from cross-functional leadership of a clinical study or part of a clinical study Excellent communication and interpersonal skills Strong strategic and critical thinking abilities Ability to manage competing priorities Desirable Skills/Experience Advanced degree, master's level education (or higher) Project management certification Proven project management experience on a global level Experience in all phases of a clinical study lifecycle At AstraZeneca, we are driven by our passion for science and our commitment to making a difference. We fuse data and technology with the latest scientific innovations to achieve breakthroughs that have never been done before. Our inclusive environment allows us to work seamlessly as one, leveraging our diverse global knowledge to create the greatest impact on disease. We are constantly advancing our scientific knowledge to shape the future of healthcare and improve patient access to life-changing medicines. If you are ready to make a significant impact on patients' lives and push the boundaries of science, apply now! We welcome your application by Aug 16th, 2026.

We're looking for a Product Developer to join our forward-thinking, dynamic team and support the development of game-changing sensor systems for the biopharmaceutical industry. Do you want to be part of a growing company of 15 that's shaping new possibilities in the field? Come join us at ArgusEye and be part of our journey! About the role: In this role, you'll design and develop advanced hardware devices that seamlessly integrate with our sensor chips, driving real impact in biopharma applications. From early idea generation to testing prototypes and final delivery, you'll take a leading role in planning, driving, and coordinating our hardware development projects. As part of our development team, you'll work across the entire product development process with a clear focus on project execution – setting direction, ensuring progress, and aligning stakeholders along the way. Your ability to combine hands-on engineering with strong project management skills will be key in bringing ideas to life and delivering reliable, high-performing products. What you'll do: Lead and drive hardware development projects from idea to finished product Solve engineering challenges and develop innovative solutions Design hardware using CAD tools Coordinate work with multidisciplinary teams and subcontractors Build prototypes, conduct tests, verify and validate designs Take an active role in shaping and improving how we run and manage hardware development projects We’re looking for someone who.. ..is driven by the opportunity to contribute to a life-critical industry through the development of advanced hardware solutions. With experience spanning the full development cycle, you’re used to taking ideas from concept to reality – planning, driving, and ensuring progress along the way. You bring a structured approach to development, where you naturally create clarity, keep momentum, and align people around a common goal to deliver high-quality results. About you: A Master's degree in Mechanical Engineering, Industrial Design, Physics, or a related field 3+ years of experience in product development Good knowledge and experience of GD&T (ISO GPS or ASME Y14.5) Skilled in CAD software (e.g., SolidWorks, or Autodesk Inventor) Proven ability to drive projects from A to Z, preferably in a regulated industry (biopharma, medtech, automotive or similar) A strong communicator who can collaborate with both technical and non-technical stakeholders Knowledge of optics, electronics, fluid mechanics, and simulation tools (e.g., COMSOL, ANSYS, Zemax) and quality systems like ISO 9001 or ISO 13485 is a bonus Why join us? Be part of a supportive, dynamic team where your contributions are valued Grow your career in an innovative, fast-paced industry Learn from our customers and attend industry and R&D conferences to grow professionally Enjoy the freedom to take ownership of your work, supported by a flexible and relaxed environment that values responsibility Experience a family-like atmosphere filled with collaboration, curiosity, and team activities like music quizzes, bowling and Friday fika About ArgusEye: ArgusEye is on a mission to revolutionize biopharmaceutical production. Today, developing life-saving medicines is often a slow, complex, and expensive process, putting vital treatments out of reach for many. By providing advanced sensor systems for real-time monitoring and control of bioprocesses, we aim to change that. Our technology, built on 40+ years of research at Linköping University, combines nanoplasmonic sensing with fiber optics to deliver real-time data, speeding up medicine development, improving efficiency, and cutting costs. With partnerships among leading pharmaceutical companies and growing demand, we're scaling to make a bigger impact. At ArgusEye, you'll be part of a close-knit team where your ideas and contributions are truly valued. Together, we're making cutting-edge technology accessible to improve lives worldwide. START: According to agreement LOCATION: Linköping JOB HOURS: Full-time CONTACT: Senior Recruiter Mikaela Ehk, mikaela.ehk@oddwork.se (contact for questions regarding the position, not applications) LAST APPLICATION DATE: Applications are reviewed on an ongoing basis As a leading recruitment and employer branding company we challenge expectations and match talents with the right corporate culture while helping organizations create stronger employer brands. Curious and want to know more? Step into the world of Oddwork by clicking here or find more career opportunities here!

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products. As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us! This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today. Key responsibilities The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO. Duties and responsibilities include: Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency. Lead root cause investigations and implement corrective and preventive actions (CAPA). Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification. Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results. Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why. Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles. Support audits and inspections by customers, regulatory authorities, and Notified Bodies. Support technology transfers from R&D to production and participate in cross-functional development projects. Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply. Skills and Competencies The suitable candidate has the following qualifications: Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related. Strong background in process engineering preferably combined with validation engineering experience. Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries). Experience with process optimization, process validation and problem solving. Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable. Experience working with Quality Management Systems. Knowledge of statistical analysis and process capability concepts. Excellent communication and documentation skills in English are required The successful candidate for this position will be someone who: Has a strong technical and analytical mindset. Enjoys solving complex manufacturing and process-related challenges. Is structured and detail-oriented. Takes ownership and drives improvements independently. Communicates effectively across departments and organizational levels. Combines hands-on problem solving with a systematic approach. Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important. We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development. About Bohus Biotech Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence. With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide. Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas: Ophthalmology – OVD solutions supporting tissue protection during cataract surgery Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform Orthopaedics – Injectable treatments for osteoarthritis All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com For more information about this position, please contact: Krishan Johansson Haque, PhD Sr Recruitment Consultant, QRIOS Life Science & Engineering T: +46 (0)72-070 16 53 E: krishan.johansson-haque@qrios.se

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger. About the Role You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements. Key Responsibilities Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes. Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance. Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices. Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes. Design and evaluate smoke studies to verify airflow performance and first-air protection. Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies. The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week. Your Profile You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind. Qualifications Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment. Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations. Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing. Proven track record leading deviation investigations, root cause analyses, and CAPA implementation. Excellent analytical, problem-solving, and technical writing skills. Strong stakeholder management and collaboration across multiple functions. Ability to independently manage complex projects and drive continuous improvement initiatives. Application If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application. About Galderma Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ, the skin, meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to over 800 professionals working across R&D, manufacturing, clinical development, and commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn. In this role you will get the opportunity to work with committed colleagues in a collaborative team. Camurus is a rapidly growing and innovative company, and you will have a strong impact on the way we work with our outsourced manufacturing activities. We are looking for an experienced Senior Outsourcing Manager to join our Manufacturing Operations team. In this role, you will be responsible for driving outsourcing programs for injectable pharmaceutical products to Contract Manufacturing Organizations (CMOs), with a particular focus on late-stage development projects. As Senior Outsourcing Manager, you will serve as the primary interface between Camurus and external manufacturing partners. This is a true Project Management role where you will ensure successful project execution from technology transfer through start of commercial production. You will work closely with internal stakeholders and external partners to secure reliable, compliant, and efficient delivery of the project. You will report to the Director Manufacturing Operations. Main responsibility Among others, your responsibilities will include: · Develop and manage project plans, timelines, and milestones for technology transfer, process development, process validation, and manufacturing readiness activities together with CMO partners. · Drive day-to-day collaboration with CMOs and ensure agreed deliverables, timelines, and performance targets are achieved. · Lead operational meetings and steering committee meetings with external manufacturing partners. · Identify risks and issues proactively and drive mitigation and resolution activities together with internal and external stakeholders. · Coordinate and manage changes with CMOs, ensuring proper documentation, implementation, and alignment with project plans and contractual commitments. · Collaborate closely with internal Camurus functions such as Quality, R&D, Regulatory Affairs and Supply Chain to ensure successful project execution. · Ensure manufacturing activities are conducted in accordance with applicable GMP requirements and regulatory expectations. · Support continuous improvement initiatives related to outsourcing, external manufacturing operations, and CMO performance. Candidate profile We are looking for a professional with extensive experience from pharmaceutical manufacturing operations including outsourcing and CMO management. You hold a Master’s degree in Engineering, Life Sciences, or a related scientific discipline. You have a solid understanding of GMP-regulated manufacturing environments and a proven track record of managing outsourcing programs and external manufacturing partners within the pharmaceutical or biotech industry. Experience from late-stage development, technology transfer and commercial manufacturing is highly valued. Experience from injectable products and combination products is considered a strong merit. As a person, you are structured, collaborative, and communicative, with a proven ability to drive complex projects and build strong relationships across multiple stakeholders. You combine a proactive and results-oriented mindset with a pragmatic and hands-on approach, while maintaining a humble and low-prestige attitude. Fluency in spoken and written and English is required. Camurus offers This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other. Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/. We are looking forward to seeing your application!

Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn. In this role, you will get the opportunity to work with committed colleagues in a collaborative team, close to both commercialised products and development projects. Camurus is a rapidly growing and innovative company, and you will have a strong impact on the outsourced manufacturing processes throughout the product lifecycle. We are looking for an experienced Senior Process Engineer to join our Manufacturing Operations team. In this role, you will be responsible for leading technology transfer activities for manufacturing processes for injectable pharmaceutical products, from development into manufacturing environments at Contract Manufacturing Organizations (CMOs). You will support products from clinical development through to commercial supply. As Senior Process Engineer, you will act as a subject matter expert in pharmaceutical manufacturing processes, working closely with internal stakeholders and external partners to ensure robust, scalable, and GMP-compliant manufacturing operations. You will report to the Director Manufacturing Operations. Main responsibility Among others, your responsibilities will include: · Lead technology transfers of injectable pharmaceutical products from development into commercial manufacturing at CMOs. · Partner with R&D to ensure that formulation and process development activities support successful scale-up, manufacturability, and long-term process robustness. · Provide technical support for process development, scale-up, validation, and commercial manufacturing activities at CMOs. · Act as technical lead for investigations and troubleshooting of process deviations, OOS results, manufacturing failures, and other complex technical challenges. · Contribute to CMC documentation in support of global regulatory submissions and product lifecycle management. · Ensure that manufacturing processes are executed in accordance with applicable GMP requirements and regulatory expectations. Candidate profile We are looking for a professional with at least 7 years of experience from pharmaceutical manufacturing operations. You hold a Master’s degree in Engineering, Life Sciences, or a related scientific discipline. You have hands-on experience from manufacturing process development, technology transfer, and GMP-regulated pharmaceutical manufacturing, preferably within sterile or injectable products. Experience from fill-finish operations and combination products development is considered a strong merit. As a person, you are collaborative, responsible, and driven by solving problems. You enjoy getting to the bottom of complex technical challenges and you are a pragmatic team player who takes ownership and follows through on commitments. At the same time, you are humble and low-prestige, always willing to support colleagues and contribute wherever needed. You thrive in a dynamic environment where technical expertise, collaboration, and problem-solving go hand in hand. Fluency in spoken and written English is required. Camurus offers This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other. Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/. We are looking forward to seeing your application!

Cleeven is an Engineering and R&D consulting group enabling our clients support in their R&D efforts and operational excellence. We have know-hows in terms of innovation and R&D in a wide range of sectors: energy, services & banking, aerospace & defence, transportation, pharmaceuticals & chemicals, as well as IT & Telecoms. We are seeking skilled and motivated mechanical engineers to join our team. As a mechanical engineer, you will be responsible for the design, analysis, and implementation of mechanical systems. Your role will involve collaborating with multidisciplinary teams to deliver innovative and efficient engineering solutions. Your responsibilities Designing and analyzing mechanical systems, components, and machinery Conducting feasibility studies and providing technical assessments Using CAE software for modeling and simulation Collaborating with cross-functional teams for product development Ensuring compliance with industry standards and regulations Qualifications Bachelor's or Master's degree in Mechanical Engineering or related field Good experience in CAD software such as CATIA or SolidWorks as well as other relevant engineering tools, for example FEM or CFD analysis Familiarity with industrial design Strong analytical and problem-solving skills Ability to work effectively in a team environment Good communication and project management abilities Currently we are recruiting 2 people, one within test and one within development. This is a permanent employment. Due to the nature of the employment, relocation in Sweden might be considered during your tenure.

Cleeven is an Engineering, R&D and IT consulting group enabling our clients support in their R&D efforts and operational excellence. We have know-hows in terms of innovation and R&D in a wide range of sectors: energy, services & banking, aerospace & defence, transportation, pharmaceuticals & chemicals, as well as IT & Telecoms. We are currently expanding our team and looking for talented and passionate software developers to join our dynamic team. As a software developer, you will play a crucial role in crafting and implementing software solutions across various projects and industries. Your responsibilities Designing, coding, and testing software applications Collaborating with engineers and stakeholders to understand project requirements Contributing to architectural design and system integration Ensuring software meets quality standards and performance metrics Continuously researching and implementing best practices in software development Qualifications Degree in Computer engineering, Electrical Engineering or similar Proven experience in software development Strong problem-solving skills and ability to work in a team environment Good communication and collaboration abilities A passion for learning and adapting to new technologies and methodologies The most common technical tools and programming languages ​​we use on our projects in this field are: Programming languages: C, C++, C# Scripting: Python, bash, Model-based development: Matlab - Simulink DevOps tooling: Jenkins, IAR compiler, GIT, gerit Documentation: Confluence Methodologies: Scrum / Agile Currently we are recruiting 2 people, one within test and one within development. This is a permanent employment. Due to the nature of the employment, relocation in Sweden might be considered during your tenure.

DOZ Apotek i Halmstad Jutaplatsen söker en driven och lyhörd apotekschef som brinner för utveckling och att leda medarbetare. Drivs du av att jobba med team och att nå en verksamhets mål? Sök då tjänsten som apotekschef redan idag, vi ser fram emot att höra från dig! Arbetsuppgifter Som apotekschef hos oss är ditt huvudsakliga ansvar att leda den dagliga verksamheten på apoteket mot de uppsatta målen. I det ingår att coacha och motivera medarbetarna till ökad försäljning, att driva apoteket kostnadseffektivt och ha god kännedom om det lokala apotekets förändrande marknadssituation. I din roll ingår budget- och personalansvar samt det övergripande ansvaret för apotekets arbetsmiljö- och kvalitetsarbete. Apotekets öppettider är: vardagar kl 08:30-18:00, lördagar kl. 09:00-14:00. Kvalifikationer Vi söker dig som brinner för utveckling, både av medarbetare och av verksamhet, samt av att nå uppsatta mål. Du är legitimerad apotekare eller receptarie, gärna med tidigare erfarenhet av arbete i apotek eller annan bransch. Det är meriterande om du har tidigare erfarenhet från en arbetsledande roll, men det är inget krav. Vi ser att du talar och skriver svenska och engelska obehindrat. Övriga språk är meriterande. Tjänsten är på heltid med 6 månaders provanställning. Personliga egenskaper Som person är du kreativ med en stark vilja att tillsammans med medarbetarna utveckla och driva apoteket framåt. Du trivs med rådgivning både vid recepthantering och egenvården och det är viktigt för dig att ge utmärkt kundservice. Du är noggrann, ansvarsfull och resultatinriktad, flexibel med en förmåga att växla mellan flera olika uppgifter utan att tappa fokus på det som är viktigt. Som person är du även nyfiken på utveckling och har ett stöttande sätt. Du drivs av att se medarbetare utvecklas samtidigt som du förstår vikten av att skapa en trivsam arbetsplats. Vi erbjuder Hos oss på DOZ Apotek får du möjligheten att vara med på en spännande resa där vi tillsammans hjälps åt att nå högre höjder, dagligen. DOZ Apotek är Sveriges nyaste apotek och vi har en vision om att alla ska få råd till en bättre hälsa och hos oss vill vi sänka trösklen till att må bra. DOZ Apotek - Råd med mera! Vår organisation präglas av korta beslutsvägar som ger dig som medarbetare möjlighet att vara med och påverka samt att utvecklas. Din personliga utveckling är viktig för oss, därför satsar vi på att alla medarbetare får den kompetensutveckling som behövs. Förutom digitala utbildningar erbjuder vi interna utbildningar inom rådgivning, egenvård, farmakoterapi, produktkunskap och ledarskap. Vi erbjuder dig möjlighet att växa med oss både på den lokala orten och inom vår internationella koncern. På DOZ Apotek arbetar vi för en jämn könsfördelning och ser mångfald som en styrka. Vi välkomnar därför kandidater med olika bakgrund, erfarenheter och perspektiv. Intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdatum – skicka gärna in din ansökan så snart som möjligt. Som en del av vår rekryteringsprocess genomför vi bakgrundskontroller för att säkerställa en trygg och säker arbetsmiljö. Bakgrundskontroller sker i slutet av rekryteringsprocessen och alltid i samråd med kandidaten. Tillsammans är vi Nytänkande, tar Ansvar, visar Respekt och har alltid Kunden i centrum. För frågor om tjänsten, kontakta Regional försäljningschef Gilbert Accaoui, 0702069386. Välkommen till ett apotek som vågar tänka nytt! DOZ Apotek arbetar dagligen för ett friskare Sverige. DOZ Apotek öppnade sitt första svenska apotek i Eskilstuna i februari 2010, då under namnet DocMorris, under åren 2013 – 2022 gick vi även under namnet LloydsApotek. Idag driver företaget ett 70-tal fysiska apotek runt om i landet och erbjuder en komplett e-handel med läkemedel och ett brett sortiment inom egenvård. DOZ Apotek är ett nytänkande apotek som genom rådgivning och tjänster vill inspirera till att leva ett mer hälsosamt liv. Hos DOZ Apotek möter kunden kompetent och välutbildad personal som är experter inom receptbelagda läkemedel, hud och värk. DOZ Apotek är en del av CEPD N.V. (Corporation of European Pharmaceutical Distributors N.V.) ett av de ledande företagen på Europas läkemedelsmarknad, med huvudkontor i Amsterdam. CEPD grundades 2008 och förvaltar den tredje största apotekskedjan i Europa med över 1500 apotek i Polen, Litauen och Sverige.

DOZ Apotek i Högdalen söker en serviceinriktad farmaceut som brinner för rådgivning och att bidra till människors hälsa. Trivs du i en roll där du möter mycket kunder? Sök då jobbet som farmaceut hos oss redan idag! Arbetsuppgifter I rollen som farmaceut arbetar du omväxlande med recepthantering, kvalificerad rådgivning av läkemedel och i egenvården, försäljning samt kvalitetsarbete. Du har en viktig roll i apoteket då du genom din kompetens bidrar med att ge bästa råd till våra kunder. En stor del av arbetet handlar om att skapa goda kundrelationer, ge service och arbeta med försäljning. Apotekets öppettider är: vardagar kl. 09:00-19:00, lördagar kl. 10:00-17:00 samt söndagar 11:00-16:00. Kvalifikationer Vi söker dig som är legitimerad apotekare eller receptarie och som gärna vill skapa goda relationer både till kunder och kollegor. Har du tidigare erfarenhet av arbete som farmaceut i apotek är det meriterande men inte ett krav. Tjänsten är på heltid/deltid med 6 månaders provanställning. Personliga egenskaper Som person trivs du med rådgivning både vid recepthantering och i egenvården och det är viktigt för dig att varje enskild kund får bästa service. Du värdesätter kunskap och vill gärna dela med dig av den. Du är noggrann, ansvarsfull och nyfiken på utveckling samt drivs av att göra skillnad. Du har en god förmåga att bygga förtroendefulla relationer både med kunder och kollegor och trivs med att arbeta i team. Vi erbjuder Hos oss på DOZ Apotek får du möjligheten att vara med på en spännande resa där vi tillsammans hjälps åt att nå högre höjder, dagligen. DOZ Apotek är Sveriges nyaste apotek och vi har en vision om att alla ska få råd till en bättre hälsa och hos oss vill vi sänka tröskeln till att må bra. DOZ Apotek - Råd med mera! Vår organisation präglas av korta beslutsvägar som ger dig som medarbetare möjlighet att vara med och påverka samt att utvecklas. Din personliga utveckling är viktig för oss, därför satsar vi på att alla medarbetare får den kompetensutveckling som behövs. Förutom digitala utbildningar erbjuder vi interna utbildningar inom rådgivning, egenvård, farmakoterapi, produktkunskap och ledarskap. Vi erbjuder dig möjlighet att växa med oss både på den lokala orten och inom vår internationella koncern. Tillsammans är vi Nytänkande, tar Ansvar, visar Respekt och har alltid Kunden i centrum. På DOZ Apotek arbetar vi för en jämn könsfördelning och ser mångfald som en styrka. Vi välkomnar därför kandidater med olika bakgrund, erfarenheter och perspektiv. Intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdatum – skicka gärna in din ansökan så snart som möjligt. Som en del av vår rekryteringsprocess genomför vi bakgrundskontroller för att säkerställa en trygg och säker arbetsmiljö. Bakgrundskontroller sker i slutet av rekryteringsprocessen och alltid i samråd med kandidaten. För frågor om tjänsten, kontakta Matea Pavic på 076 233 74 79 Välkommen till ett apotek som vågar tänka nytt! DOZ Apotek arbetar dagligen för ett friskare Sverige. DOZ Apotek öppnade sitt första svenska apotek i Eskilstuna i februari 2010, då under namnet DocMorris, under åren 2013 – 2022 gick vi även under namnet LloydsApotek. Idag driver företaget ett 70-tal fysiska apotek runt om i landet och erbjuder en komplett e-handel med läkemedel och ett brett sortiment inom egenvård. DOZ Apotek är ett nytänkande apotek som genom rådgivning och tjänster vill inspirera till att leva ett mer hälsosamt liv. Hos DOZ Apotek möter kunden kompetent och välutbildad personal som är experter inom receptbelagda läkemedel, hud och värk. DOZ Apotek är en del av CEPD N.V. (Corporation of European Pharmaceutical Distributors N.V.) ett av de ledande företagen på Europas läkemedelsmarknad, med huvudkontor i Amsterdam. CEPD grundades 2008 och förvaltar den tredje största apotekskedjan i Europa med över 1500 apotek i Polen, Litauen och Sverige.