Boss Business Partner är ett rekryterings- och bemanningsföretag i Mora. Vi erbjuder våra kunder interimlösningar och möjligheten att hyra in konsulter inom tjänstemannasektorn. Efterfrågan på våra tjänster ökar och vi söker nu dig som vill jobba som konsult eller intresserade av tjänster ute hos någon av våra kunder Vi söker dig med erfarenhet som; Bygg och anläggning- projektledare, arbetsledare eller verksamhetsutvecklare Ekonomi- ekonomiassistent, controller, ekonomiansvarig, ekonomichef, redovisning Marknadsföring- digital marknadsförare eller chef Industri- arbetsledare eller andra ledande befattningar Hållbarhet- strateg, koordinator och controller HR- administratör, generalist, arbetsmiljö- och arbetsrättsspecialist Inköp- assistent, strategisk eller operativ inköpare Om dig Vi söker dig som trivs med att arbeta i en föränderlig miljö och har en förmåga att snabbt anpassa dig till nya sammanhang. Som konsult hos oss är det viktigt att du är flexibel och snabbt kan hitta din plats i olika företag och organisationer. Du har en naturlig förmåga att kommunicera och samarbeta med olika typer av människor och känner dig trygg i att bidra med din expertis oavsett bransch eller uppdragets karaktär. Vi ser att du är lösningsorienterad, självgående och tycker om att ta dig an nya utmaningar. Med ditt driv och din professionella inställning bidrar du till att våra kunder får den bästa lösningen på sina behov. Tidigare erfarenhet av konsultuppdrag är meriterande, men viktigast är att du har rätt inställning och vilja att utvecklas i rollen. Vi tittar löpande på ansökningar som kommer till oss så tveka inte att skicka in ditt CV eller skriv en rad om dig själv. Vid frågor är du välkommen att kontakta oss, Sofia [email protected] eller Evelyn [email protected]

Magle Group is growing and we are looking Regulatory Affairs Specialist who is looking for a new challenge and who wants to be part of a small but dynamic regulatory team. Magle Group is supporting other Life Science Companies by providing CDMO services as well developing and manufacturing our own products with DSM technology. This role will focus on supporting our medical devices business and assure we comply with all regulatory standards and guidelines applicable in our active markets. The Regulatory Affairs Specialist plays a crucial role in the submission, registration, and lifecycle management of our medical device products. Key Responsibilities: Prepare and submit regulatory documentation required for the approval and registration of new and existing products in various international markets. Be updated of regulatory procedures and changes in the regulatory climate to ensure compliance and advise the company on necessary adjustments. Legalization of registration documentation. Inform and educate the organisation on submission requirements and ensure necessary documents are provided. Maintain regulatory files and update regulatory authorizations, such as Investigational Device Exemptions (IDEs), 510(k) submissions, Canadian medical device licenses, and CE dossiers for the EU, as well as NRTL certifications. Maintenance of registrations , renewals, device listings, site registrations, supplements for changes, and annual reports. Respond to questions from regulatory authorities. Change control activities Assess device-related incidents and complaints for medical device reporting requirements. Compile and submit reportable events to relevant regulatory authorities in a timely manner. Handle recalls and field actions, if required. Review and create product labels and review promotional materials to ensure compliance with applicable regulations and technical standards. Assist in preparing clinical trial site ethics review board applications for investigational device trials. Prepare interim or final reports for trial site ethics boards as required. Other duties as assigned to support the regulatory team and ensure compliance with global regulatory requirements. Qualifications: Bachelor’s degree in a scientific or related field; advanced degree preferred. Minimum of 5 years of experience in regulatory affairs, specifically with medical devices. Strong understanding of international regulatory guidelines and standards such as FDA, CE Marking, NBOG, ISO 13485, MDR etc. Proven track record in preparing successful regulatory submissions. Excellent communication skills, both written and verbal, with the ability to interact effectively at all levels of the organization and with regulatory authorities. Highly organized and able to manage multiple projects simultaneously in a fast-paced environment. Meriting: Experience with Class II and Class III medical devices. Experience with APIs including CEP and ASMF files, is a plus. Familiarity with regulatory landscape in key international markets (e.g., Europe, Asia, and North America). Proficient with regulatory submission software and document management systems. The position is located in Malmö on-site. If you find the above position interesting, it fits your experience, and you want to join a company that has an interesting journey ahead, we would love to hear from you. We are a value driven organisation, and we expect you to share our passion to make an impact by making lives better for patients worldwide. Therefore we also look to find a person who not only fits the qualifications but also shares our values and fits our organisation personality wise. In this process we will have a continuous recruitment. Please submit your CV and a short cover letter telling us why you find the position interesting. The position is placed at our office in Malmö and will be a full-time position. To find out more about us please visit our group web page: www.maglegroup.com

Who we are Olink, part of Thermo Fisher Scientific, is transforming the understanding of human diseases through advanced proteomics. We are driven by a commitment to innovation, quality, and transparency, providing exceptional solutions and support for human protein biomarker discovery. For many years, the critical role of proteins in human biology has been recognized, but technological constraints limited comprehensive research into their potential across various biological processes and diseases. With our innovative Olink solutions, scientists can now measure thousands of human proteins simultaneously using just a few microliters of blood. Our highly specific and validated assays cover a wide dynamic range, empowering groundbreaking research. Our services include flexible protein biomarker solutions, with a robust library of thoroughly validated assays covering ~5000 proteins. As we expand globally, we continue to play a pivotal role in shaping the future of scientific discovery. To learn more, visit www.olink.com. Position Description We are seeking a highly motivated and experienced Scientist to join our Affinity Evaluation qPCR Section within the Highplex Department, enabling the development of new highplex products. As Scientist you will participate in research and development of product ideas and products as well as routine screening in accordance with project plans and work schedules. The position involves laboratory work, analysis and documentation. In this role you would report to the Section Manager Affinity Evaluation qPCR and be based in our Uppsala headquarters. Primary Responsibilities Actively lead and/or participate in section-, project- and department activities, and the development of product concepts and ideas. Participate as project member in meetings and project planning. Independently plan and execute laboratory work in accordance with set project plans and work schedules as well as evaluating and documenting results. Handle and prepare antibodies, antigens and biological samples for experiments. Perform PEA-experiments, mainly using qPCR as a readout. Develop new and continuously improve existing procedures, protocols and analysis methods. Perform verification studies and contribute to analyzing data shared with customers. Qualifications Ph.D. in a relevant life sciences field (e.g., Molecular Biology, Biochemistry, Biotechnology, Immunotechnology) or equivalent experience. Two or more years of working experience from an industry setting. Documented lab experience. Extensive scientific and technical knowledge in molecular biology, proteomics and biochemistry. Experience with assay development of antibody-based test methods as well as working with and optimizing PCR/qPCR and DNA sequencing (NGS). Experience of lab automation, pipetting robots and different conjugation chemistries is advantageous. Proven experience of data analysis. Experience with R and handling of large data sets is a preferable. Good general computer skills and expert level knowledge of Excel. Experience of working in, and driving projects. Good communication skills in written and spoken English, Swedish skills is a plus. Soft Skills As a person youare a team player who treats people with respect and finds it easy to communicate with others, both within the team and cross-functionally. You love to solve problems by thinking outside the box and drive development initiatives forward in cooperation with others. Finally, you are a positive person who is flexible in terms of your daily tasks. If you are a driven scientist with a passion for developing innovative protein assays and want to be part of a team at the forefront of biotechnology, we encourage you to apply. Please submit your resume and a cover letter detailing your relevant experience and why you are the ideal candidate for this position. The last application date is on the 30th of March. The selection process is ongoing and the position could get filled before the last application date.

Arbetsuppgifter Avdelningen för Kvant- och Nano-fysik söker Mastersstudenter för sommararbetare som Labbassistent med forskning inom kvantteknologi. Personen som få tjänsten kommer att arbeta tillsammans med Doktorander och Postdoktorer med uppgifter som kan omfatta:  simulation, design, mikro och nano-fabrikation, kryoteknik, mikrovågselektronik, optiskmätteknik och dataanalys. Aktiv forskningsprojekt inom avdelningen syftar på kvantbegränsadmätningar kvantkommunikationen och kvantinformationbehandling.  Vi erbjuder - En anställning på ett ledande tekniskt universitet som skapar kunskap och kompetens för en hållbar framtid - Engagerade och ambitiösa kollegor samt en kreativ, internationell och dynamisk miljö - Handfast erfarenhet med avancerad utrustning och experimentalfysik Kvalifikationer Krav - Du ska vara antagen till utbildning på grund- eller avancerad nivå vid svenskt lärosäte Meriterande - Student på KTH - Mastersstudent i tillämpad fysik med avklarade kurser inom Kvantteknologi och Kvantfysik på avancerad nivå Vi kommer att lägga stor vikt vid personliga egenskaper. Fackliga representanter Kontaktuppgifter till https://www.kth.se/om/work-at-kth/fackrepresentanter-1.500898 Ansökan Du ansöker via KTH:s rekryteringssystem. Du som sökande har huvudansvaret för att din ansökan är komplett när den skickas in. Din kompletta ansökan ska vara KTH tillhanda senast sista dagen för ansökningsperioden Om anställningen Anställningen gäller tidsbegränsat enligt avtal - i upp till 3 mån, med tillträde enligt överenskommelse. Amanuenstjänsten är avsedd för sommararbete mellan 1 juni och 31 augusti.  De exakta veckorna för arbetet kommer att schemaläggas i diskussion med den anställde. Tjänsten är avsedd för Mastersstudenter som ett sommarjobb, mellan deras kursarbeten under vår och hösttermin.   Sommarjobb kommer att bjudas till kvalificerad sökande beroende på tillgång till finansiering.  Övrigt Strävan efter jämställdhet, mångfald och lika villkor är både en kvalitetsfråga och en självklar del av KTH:s värdegrund. För https://www.kth.se/om/work-at-kth/processing-of-personal-data-in-the-recruitment-process-1.823440 i samband med rekrytering. Det kan förekomma att en anställning hos KTH är placerad i säkerhetsklass. Om så är fallet för just denna anställning görs en säkerhetsprövning av sökande i enlighet med säkerhetsskyddslagen (2018:585) efter samtycke. I dessa fall är en förutsättning för anställning att sökande blir godkänd efter säkerhetsprövning. Vi undanber oss direktkontakt med bemannings- och rekryteringsföretag samt försäljare av platsannonser.   Om KTH KTH är ett av Europas ledande tekniska universitet och en viktig arena för kunskapsutveckling. Som Sveriges största universitet för teknisk forskning och utbildning samlar vi studenter, forskare och fakultet från hela världen. Vår forskning och utbildning omfattar såväl naturvetenskap som alla grenar inom teknik samt arkitektur, industriell ekonomi, samhällsplanering, historia och filosofi. https://www.kth.se/om/om-kth-1.885102

Who we are Olink, part of Thermo Fisher Scientific, is transforming the understanding of human diseases through advanced proteomics. We are driven by a commitment to innovation, quality, and transparency, providing exceptional solutions and support for human protein biomarker discovery. For many years, the critical role of proteins in human biology has been recognized, but technological constraints limited comprehensive research into their potential across various biological processes and diseases. With our innovative Olink solutions, scientists can now measure thousands of human proteins simultaneously using just a few microliters of blood. Our highly specific and validated assays cover a wide dynamic range, empowering groundbreaking research. Our services include flexible protein biomarker solutions, with a robust library of thoroughly validated assays covering ~5000 proteins. As we expand globally, we continue to play a pivotal role in shaping the future of scientific discovery. To learn more, visit www.olink.com. Position Description We are on an exciting growth trajectory, and we are thrilled to announce an opportunity for a passionate and skilled Project Manager to join our Project Management Office (PMO). Our PMO, a dedicated team of 8 project managers, spearheads the most strategic and impactful projects aligned with our visionary goals. As a Project Manager at Olink, part of Thermo Fisher Scientific, you will be at the forefront of innovation in proteomics, driving a variety of projects including New Product Introductions (NPI) and diverse business initiatives. Your role will be pivotal in ensuring the continued success and advancement of our cutting-edge products. This position is based at our Uppsala office and reports directly to the Head of PMO. If you are ready to make a significant impact and contribute to the future of proteomics, we would love to hear from you! Primary Responsibilities As Project Manager you will be responsible for leading and delivering strategic projects according to set timeframe and budget. This could include, but is not limited to, the following tasks: Develop a timetable for the projects according to set goals. Lead projects towards agreed goals according to set schedule, quality and budget. Collaborate with project stakeholders internally and externally. Responsible for communication with the Steering Committee. Continually work to improve, educate and lead within Olink's project processes. Develop, manage and drive improvements through engagement, support teamwork and apply structured models in project management. Qualifications/skills Relevant degree in a related field (Bsc, MSc, PhD in Engineering, Life Sciences) Certification in Project Management (e.g PMP, IPMA etc) is highly beneficial. At least a few years of experience in project management or product management within the Life Science industry. Experience of NPI projects is highly advantageous. Professional proficiency in both Swedish and English is mandatory and necessary to be successful in this role. As a person you are responsive, curious and committed. You are a solution-focused leader who thrives in a dynamic and fast-paced environment. Furthermore, you are a team player who is good at communicating with different stakeholders and who can see things from different perspectives. To be successful in this role you should also be pragmatic and meticulous when needed and be able to see things from a long-term, strategic perspective. The selection process is on-going, and the position might get filled before the last day of application so please apply as soon as possible, however no later than 2025.03.30. If you want to help to deepen the understanding of real-time human biology and are looking for an exciting new challenge, we encourage you to apply!

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.

Who we are Olink, part of Thermo Fisher Scientific, is transforming the understanding of human diseases through advanced proteomics. We are driven by a commitment to innovation, quality, and transparency, providing exceptional solutions and support for human protein biomarker discovery. For many years, the critical role of proteins in human biology has been recognized, but technological constraints limited comprehensive research into their potential across various biological processes and diseases. With our innovative Olink solutions, scientists can now measure thousands of human proteins simultaneously using just a few microliters of blood. Our highly specific and validated assays cover a wide dynamic range, empowering groundbreaking research. Our services include flexible protein biomarker solutions, with a robust library of thoroughly validated assays covering ~5000 proteins. As we expand globally, we continue to play a pivotal role in shaping the future of scientific discovery. To learn more, visit www.olink.com. Position Description We are now looking for a Development Engineer to join the Assay Development NGS team within the Highplex department, RnD. If you want to work with a world-leading technology that contributes to the development of precision medicine, you might be the person we are looking for. Assay Development NGS has the main responsibility to develop immunoassays for the Olink Highplex products and to evaluate assay performance throughput development projects. This includes performing verification experiments and generating assay performance data for website. Product development is carried out in projects with members from other departments. Further more, Assay Development NGS also contributes to research and development of product concepts and ideas. Assay Development NGS currently consists of 10 people, but since the company is growing rapidly with very exciting things going on, the group needs to be expanded with additional members. Primary Responsibilities As a Development Engineer in the group, your duties will vary across project phases. It will consist of both laboratory work, but also data analysis and logging of information. The main tasks will be to: Perform experiments using Olinks PEA (Proximity Extension Assay) with NGS as a readout platform. Plan and perform laboratory work in accordance with set project plans and work schedules. Evaluate, report and document results from the laboratory work according to existing procedures. Handle and register data for large amounts of antibodies, antigens and biological samples. Actively participate in the development of the group's and department's activities and participate in improvement projects. Qualifications/skills Master’s degree in life sciences or corresponding education. Documented lab experience and a few years of working experience from the industry. Experience in pipetting small volumes and of using pipetting robots is advantageous. Experience with antibody-based test methods as well as with PCR and NGS. Experience with handling and characterizing biological samples, with a focus on plasma and serum is advantageous. Good computer skills in general and good knowledge of Excel. Experience of using python or R-scripts are advantageous. Experience of working in projects. Fluent in spoken and written English, Swedish is a plus. As a person you are responsible, driven, proactive and solution oriented. As we handle large amounts of reagents and data, we value that you are thorough and structured. You are a team player who finds it easy to communicate and interact with others both within the group and with those who work in other departments and functions. It is important that you have a positive attitude and can adapt to changing circumstances. The selection process is on-going, and the position might get filled before the last day of application so please apply as soon as possible, however no later than 2025.03.23.. If you want to help to deepen the understanding of real-time human biology and are looking for an exciting new challenge, we encourage you to apply!

Who we are Olink, part of Thermo Fisher Scientific, is transforming the understanding of human diseases through advanced proteomics. We are driven by a commitment to innovation, quality, and transparency, providing exceptional solutions and support for human protein biomarker discovery. For many years, the critical role of proteins in human biology has been recognized, but technological constraints limited comprehensive research into their potential across various biological processes and diseases. With our innovative Olink solutions, scientists can now measure thousands of human proteins simultaneously using just a few microliters of blood. Our highly specific and validated assays cover a wide dynamic range, empowering groundbreaking research. Our services include flexible protein biomarker solutions, with a robust library of thoroughly validated assays covering ~5000 proteins. As we expand globally, we continue to play a pivotal role in shaping the future of scientific discovery. To learn more, visit www.olink.com. Position Description We are seeking a highly motivated and driven Development Engineer to join our Midplex team within R&D, responsible for the development of our Midplex products. In the Midplex product area, we are focusing on products that via qPCR-based quantification measure up to 100 proteins simultaneously. In this role, you will take an active part in research and development projects, developing and optimizing new assays and actively contributing to development of product concept and ideas. You will have the opportunity to work on new and exciting projects, collaborate with cross-functional teams, and contribute to the development of future innovative products. The position will be based in our Uppsala headquarters. Primary Responsibilities Actively participate in development of product concepts and ideas within the area of the Midplex product portfolio. Plan and design laboratory experiments to validate and optimize protocols and technical solutions. Evaluate, report and document results in technical reports and presenting results. Analysis of data sets, applying statistical methods as needed to interpret data and draw conclusions. Develop and improve existing and new procedures, protocols and analysis methods. Collaborate closely with cross-functional teams to translate customer needs into product specifications. Qualifications University degree in life sciences (e.g., Biochemistry, Molecular Biology, Immunology) or corresponding education. At least a couple of years of experience in development work within the field. Documented skills and experience in laboratory work (e.g., DNA sequencing techniques such as PCR, qPCR and NGS). Experienced in the development of protein assays, such as PEA, ELISA or other relevant techniques. Familiarity with relevant software and data analysis tools. Fluent in English, Swedish is a plus. We believe that you are inclusive, driven and pragmatic. You enjoy working in a team and communicating with lots of different people. You have an analytical mindset and you are motivated by solving all kinds of problems and you pay attention to details. It’s also important that you are adaptable and enjoy a high work pace. The last day for applying is on the 23.03.2025 but please submit your application as soon as possible. If you want to help to deepen the understanding of real-time human biology and are looking for an exciting new challenge, we encourage you to apply!

Overview Atley Solutions is a global leader in commercial products and services for the development and manufacturing of radiopharmaceuticals based on Astatine-211. These pharmaceuticals are used in targeted alpha therapy, a promising treatment modality for metastatic cancer. With a strong track record of industry partnerships and a commitment to innovation, our team is at the forefront of advancing cancer therapies that make a real difference in patients’ lives. Atley is a dynamic, globally-minded startup and has been recognized as one of Sweden’s most innovative technology startups by Ny Teknik in 2021, 2023, and 2024. We are seeking a talented Radiochemist to join our close-knit team and contribute to breakthrough solutions in life sciences. About the Role As a Radiochemist at Atley Solutions, you will be an integral part of our research and development efforts. Your responsibilities will include: Radiochemistry Development & Automation – Design and optimize radiochemistry processes and automation workflows. Supporting Early Drug Discovery – Collaborate on customer projects to advance novel therapies. Technology Advancement – Contribute to the in-house development and refinement of Atley’s proprietary technology. Customer Engagement – Work directly with clients, including installation and maintenance of Atley hardware products at customer sites, with occasional travel within Sweden and internationally. Work Environment: You will be based at a unique research lab at Sahlgrenska University Hospital in Gothenburg, Sweden, working alongside globally recognized key opinion leaders (KOLs) in Astatine radiochemistry, including Emma Aneheim and Sture Lindegren. About You We are looking for an individual who is: Qualified – Holds a degree in Chemistry, Chemical Engineering, or a related field (open to both recent graduates and candidates with prior experience). Collaborative – Thrives in a team environment where initiative and responsibility are highly valued. Adaptable – Willing to travel as needed for product installations and maintenance. Communicative – Proficient in written and spoken English, ensuring effective communication with international stakeholders. Note: While prior experience in radiochemistry is not required, a strong foundation in chemical laboratory work is essential for success and professional growth in this role. Join Us Atley Solutions offers a supportive, forward-thinking environment where every team member plays a vital role in shaping the future of healthcare. If you are passionate about (radio)chemistry and eager to make a transformative impact in life sciences, we invite you to apply. To apply, please submit your resume and cover letter detailing your qualifications and interest in the Radiochemist role. We look forward to hearing from you!

Temporary position as Laboratory Engineer at Immuneed, a life-science company in Uppsala Immuneed provides services to pharmaceutical and biotechnology companies and specializes in immunology and drug development. Our service is based on a unique technology developed through extensive research both at Uppsala University and Immuneed, which aims to make pharmaceuticals safer and better for patients. We are now searching for a replacement while one of our Laboratory Engineers is on parental leave from May 5th to November 5th, 2025. The starting date can be discussed. About the position as Laboratory Engineer You will work together with our dedicated lab team and, after training, perform our key assay ID.Flow, which involves taking blood samples from healthy volunteers who come to our site and transferring the blood to the system together with the pharmaceuticals that we are studying for our customers. After incubation, samples are analysed using different assays like flow cytometry and ELISA. Further, the job involves maintenance of the laboratory, preparations of materials, documentation, and analyses of the raw data using primarily Excel. You are someone who enjoys working in a lab, learning new techniques, and a varied schedule of intense days with complicated assays and calm days with routine work. You are thorough, structured, flexible, and able to sometimes handle stressful situations. Furthermore, you can work independently but also enjoy working as a team. You will report to the Laboratory Manager. Qualifications • Biomedical Analyst (BMA) degree or equivalent (graduation in June is satisfactory). • Mandatory qualification: Knowledge of blood sampling and being comfortable with taking blood samples from healthy volunteers. • Laboratory experience, including whole blood assays, ELISA, and flow cytometry. • Good knowledge of Excel/Word. • Good verbal and writing skills in Swedish and English. • Experience working in a GLP-certified lab. If you find this opportunity interesting, please apply as soon as possible but at the latest 14th of March 2025 . Welcome with your application! Interviews are ongoing during the process and the recruitment might be closing before last day of application.