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Rensa sökfilterProjektledare inom Life Science
Vill du vara med och säkerställa kvaliteten inom Life Science tillsammans med branschens skarpaste hjärnor? Då är det här du ska vara. Hos oss väntar uppdrag som kräver nyfikenhet, lösningsdriv och vass kompetens och som ger dig chansen att utvecklas i nya sammanhang. Tillsammans bidrar vi till en bättre morgondag och formar framtidens lösningar som gör skillnad för människor och samhälle. Det här blir din roll Som projektledare hos oss leder du uppdrag inom Life Science – en bransch där precision, struktur och kvalitet är avgörande. Du säkerställer att rätt processer, system och miljöer är på plats, med fokus på hög standard, säkerhet och regelefterlevnad. Exempel på projekt vi kan stötta är ombyggnationer och flytt av laboratorier, renrum eller andra specialanpassade GxP-klassade lokaler, implementering av nya IT-system och utrustning, tech transfer samt kvalificering och validering av lokaler, utrustning och processer inom regelstyrda miljöer. Detta är en delad roll där din specialistbakgrund gör det möjligt för dig att operativt leverera i projekt såväl som att leda dem. Rollen innebär att du: Leder, koordinerar och strukturerar projekt i samverkan med olika funktioner Ansvarar för projektets budget, tidplan och leveranser Skapar förståelse och samsyn mellan teknik, verksamhet och kund genom tydlig kommunikation Identifierar och hanterar intressenter, risker och beroenden Motiverar och engagerar projektteamet för att nå gemensamma mål Vi har kontor på flera orter i Sverige. Den här tjänsten är placerad vid vårt kontor i Kista, och projekten sträcker sig över hela Mälardalsregionen. Så här kommer du att briljera Hos oss blir du en del av ett kompetent och engagerat team som driver projekt med trygghet, samarbete och ansvar som grund. Vi erbjuder en arbetsmiljö som präglas av flexibilitet, balans och gemenskap – och du får tillhöra ett kunskapsdrivet företag med stark kultur och samhällsnytta i fokus. Genom en personlig utvecklingsplan stöttar vi både din professionella och personliga utveckling. För att lyckas i rollen ser vi att du har: Relevant högskoleutbildning, exempelvis inom kemiteknik, medicinteknik, bioteknik eller liknande Erfarenhet inom QA/RA eller Validering Minst två års erfarenhet av projektledning eller koordinering i en regelstyrd miljö, där du har arbetat med budget, tidplan och resursstyrning Bred kunskap och en dokumenterad förmåga att snabbt sätta dig in i nya områden En kommunikativ och relationsskapande personlighet med förmåga att engagera och skapa förtroende på olika nivåer i en organisation Mycket goda kunskaper i både svenska och engelska, i tal och skrift Det är meriterande om du även har: Fördjupad kunskap om relevanta regelverk och standarder inom Life Science, såsom GMP, GDP, GCP, ISO 13485, ISO 9001, ISO 15189, FDA etc. Erfarenhet av projekt inom datoriserade system eller supply chain Tidigare erfarenhet från konsultrollen eller av att arbeta i uppdragsbaserade miljöer Att vara en del av Team PV Vi är ett konsultbolag som brinner för Life Science, från MedTech-startups till globala läkemedelsbolag. Hos oss får du följa hela kedjan, från tillverkning till vård, och arbeta med regelverk, revisioner, projektledning och utvärderingar. Det som driver oss är att hjälpa kunder nå sina mål och göra verklig skillnad för patienter och samhälle. Hos oss får du något annorlunda. Vi skiljer oss från traditionella konsultbolag genom vår unika kultur, den sticker ut och genomsyrar allt vi gör och vi är extremt stolta över att vara ett Great Place To Work, år efter år. Vissa säger att en kultur sitter i väggarna. Om vår hade gjort det, hade vi haft mjuka väggar. Välkommen till oss på Plantvision! Ansökan Välkommen att skicka in din ansökan så snart som möjligt. Urval och intervjuer sker löpande. Om du har frågor om denna tjänst, välkommen att kontakta Cecilia Almkvist på 076 102 66 68 eller cecilia.almkvist@plantvision.se Har du eget bolag och är intresserad av att samarbeta med oss som underkonsult? I stället för att söka en specifik tjänst, connecta gärna med oss via vår karriärsida och ange att du är intresserad av att gå som underkonsult – så hör vi av oss när något passande dyker upp.
Researcher in Biomedicine
We are looking for a researcher in biomedicine for a fixed-term position at the School of Medical Sciences. Subject area The subject area for this position is biomedicine. Background We are looking for a researcher in biomedicine to contribute to interdisciplinary research in cardiovascular biomedicine, funded by the Knowledge Foundation. The research focuses on understanding mechanisms underlying cardiovascular disease, particularly in the context of inflammation, infection and vascular pathology, and on developing advanced experimental models to investigate these processes. The work integrates human cell-based models, advanced 3D multicellular systems, molecular and functional characterization, and omics-based approaches to investigate mechanisms of cardiovascular injury and disease progression. Particular emphasis is placed on inflammation and infection in the context of cardiovascular disease, vascular inflammation, and the development of physiologically relevant experimental models that bridge mechanistic research and human disease. The research is conducted at Örebro University within a multidisciplinary environment and in collaboration with academic, clinical, international and industry partners. This provides opportunities to work across complementary experimental platforms and contribute to translational research aimed at improving our understanding of cardiovascular disease and supporting the development of future preventive and therapeutic strategies. Duties and responsibilities The current position is aimed at supporting and further developing research with a focus on experimental cardiovascular biomedicine, including studies of inflammatory, infectious and environmental factors relevant to cardiovascular disease, vascular inflammation, and advanced human-relevant models that link molecular and cellular findings to disease mechanisms and clinical relevance. The work includes advanced cell culture of various cardiovascular cell types, 3D cell models, spheroids and organoids, infection-related experimental models, flow cytometry, microscopy, and molecular and functional cellular characterization. The researcher is expected to independently plan, conduct, analyse and interpret experimental studies and to contribute to the development, optimization and implementation of experimental methodologies within the research projects. The duties also include scientific publication and presentation of research findings, supervision of students, and collaboration with national and international research partners. Qualifications Those qualified for the appointment as a researcher are applicants who have obtained a doctoral degree or have a degree from abroad deemed to correspond to a doctoral degree. Assessment criteria As a general assessment criterion, the applicant must be able to demonstrate the personal qualities required to perform the relevant tasks, the ability to collaborate with other staff and the ability to contribute to the development of the research. We are looking for a candidate with documented experience in experimental biomedical research and a strong background in infection biology and host-pathogen interactions, together with knowledge relevant to cardiovascular disease. Knowledge of atherosclerosis and its underlying inflammatory mechanisms is particularly advantageous. Experience in advanced mammalian cell culture, 3D cell models, spheroids, organoids or organ-on-chip systems, and experimental approaches for studying infection, inflammation or host responses is considered a merit. Experience in multiparameter flow cytometry, fluorescence or confocal microscopy, and molecular and immunological methods is also advantageous. Experience with cardiovascular cell models, animal models (including mice experiments), vascular calcification, human iPSC-derived cells, and omics-based approaches will be considered an additional merit. Particular importance will be placed on scientific competence, documented experimental research experience, and the ability to independently plan, conduct and analyse experimental studies. Experience of multidisciplinary and translational research is advantageous. Good oral and written communication skills in English are required. Information This is a fixed-term full-time position (100%) for 12 months. At Örebro University, salary depends on the successful candidate’s qualifications. For more information about the position, contact Geena Paramel Varghese, +46 19 30 38 01, email: geena.paramel@oru.se (PI KKS-Synergi), or Simon Athlin, +46 70 265 88 80, email: simon.athlin@oru.se (Head of unit). At Örebro University, we expect each member of staff to be open to development and change; take responsibility for their work and performance; demonstrate a keen interest in collaboration and contribute to development; as well as to show respect for others by adopting a constructive and professional approach. Örebro University actively pursues equal opportunities and gender equality as well as a work environment characterized by openness, trust and respect. We value the qualities that diversity adds to our operations. Application The application is made online. Click the button “Apply” to begin the application procedure. For the application to be complete, the following electronic documents must be included: Covering letter, outlining how you believe you can contribute to the continued development of Örebro University CV with a relevant description of your overall qualifications and experience Account of research qualifications and experience Copies of relevant course/degree certificates and references verifying eligibility and criteria met Only documents written in Swedish, English, Norwegian and Danish can be reviewed. More information for applicants will be found on our career site: https://www.oru.se/english/career/available-positions/applicants-and-external-experts/ The application deadline is 2026-10-16. We look forward to receiving your application! As we have already made our choices in terms of external collaboration partners and marketing efforts for this recruitment process, we decline any contact with recruitment agencies and advertisers. As directed by the National Archives of Sweden (Riksarkivet), we are required to deposit one file copy of the application documents, excluding publications, for a period of two years after the appointment decision has gained legal force.
Regulatory System Manager
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. As a Regulatory System Manager you'll get the chance to interpret different regulations as they apply to Cytivas products, processes and procedures. You will also advise on impact of regulations, devises strategies for compliance, and liaison with regulatory bodies. The position will also work with investigations and resolve compliance problems, questions and complaints. Audits and evaluates current policies, procedures, and documentation will also be a part of the responsibilities. This position reports to the Sr. Regulatory Manager for chemical and consumable products and is a part of the Product Regulatory Compliance department located in Uppsala. What You'll Do Maintain and manage regulatory documentation used in NPDs (New Product Development) to secure compliance to relevant regulations for market access, e.g. safety data sheets Coordinate and collaborate with IT to ensure regulatory systems are up to date and integrated with other Cytiva systems, including acquired businesses Support other users of regulatory systems in how to best create compliant documentation Monitor and review change requests/orders and regulatory changes to ensure that compliance requirements are met and maintained. Drive simple, cost-efficient and pragmatic solutions to issues related to regulatory requirements in NPDs and other projects. Who you are Bachelors' Degree in Chemistry, Biochemistry or related field with a few years relevant working experience Experience with Product regulations, QA/RA, other regulatory areas or experience with Cytiva’s product portfolio and an interest to learn about regulatory compliance. Knowledge around the Cytiva portfolio Knowledge around environmental and chemistry regulations, e.g. familiar with REACH, GHS labeling, hazardous chemicals, and similar regulations Familiarity and interest in maintaining IT systems It would be a plus if you also possess previous experience in: Communicating with authorities, e.g. chemistry and border control authorities Written and spoken Swedish
Senior Scientist/Staff Research Engineer
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Senior Scientist/Staff Research Engineer is responsible for scientific/technical leadership in downstream purification of biologic molecules. We are looking for a candidate with strong application expertise in plasma, including process development and biopharmaceutical manufacturing process understanding. In this role you will have the opportunity to turn new ideas into purification products for our customers around the globe. This position reports to the Senior Section Manager for Capture Applications within the Start-to-Finish Department in R&D, which is part of the Resins & Technologies Business Unit located in Uppsala, Sweden and will be an on-site role. The Start-to-Finish team focuses on applications for customers’ complete end-to-end processes and thought leadership. What you will do: Actively contribute in Research, New Product Development and Market Support projects as a chromatography subject matter expert. Design, evaluate and optimize new plasma purification solutions. Act as scientific/technology mentor within R&D and as lead/expert in external collaborations and customer support. Act as activity leader in project work. Contribute to scientific presence presenting posters and orals at conferences. Who you are: PhD or MSc in Biotechnology/Biochemistry/Chemical engineering or corresponding relevant field. At least 5 years’ experience as a Scientist/Senior Research Engineer. Practical experience in chromatography purification of biomolecules in the biopharmaceutical field and subsequent analytic methods. Excellent communication skills. Ability to motivate and lead. Advanced English language (oral and writing), working proficiency in Swedish language. It would be a plus if you also possess previous experience in: The Biopharma/Biologics Industry
Hands-on Regulatory Affairs Expert
Sunmedic is a medical device company focused on developing safe and effective products. We are looking for a hands-on Regulatory Affairs Expert who can take ownership of technical documentation, ensure regulatory compliance, and work closely with quality and development teams. What you will do - Prepare, maintain, and update technical files and regulatory documentation in line with EU MDR and other applicable regulations. - Handle regulatory submissions (EU MDR) and manage lifecycle activities including updates and variations. - Support and maintain the quality management system (ISO 13485), including quality control documentation and records. - Review and assess design changes, labeling updates, and material changes for regulatory impact. - Collaborate with Quality Assurance and R&D teams to ensure technical documentation is complete, accurate, and audit-ready. - Prepare for and support audits and inspections by notified bodies and competent authorities. - Contribute to post-market surveillance activities and the preparation of related reports (e.g., PMCF, PSUR). - Monitor regulatory updates and implement necessary changes in technical files and quality documentation. Who you are - A practical and detail-oriented regulatory professional who enjoys working directly with technical files and documentation. - Comfortable working in a fast-paced environment where you need to deliver concrete regulatory outputs. - Proactive in identifying compliance gaps and implementing practical solutions. - Clear communicator who can work effectively with Quality, R&D, and external auditors. What you have - Bachelor’s or Master’s degree in Life Sciences, Engineering, or a related field. - At least 2 years of ,hands-on regulatory affairs experience, in the medical device industry. - Solid experience preparing and maintaining, technical files, and working within a quality management system (ISO 13485). - Good knowledge of EU MDR requirements and regulatory submissions. - Strong organizational skills and attention to detail when managing documentation and multiple tasks. - Proficiency in English (written and spoken). Nice to have: - Experience with post-market surveillance and clinical evaluation reports. - Familiarity with US FDA 510(k) or UK MDR submissions. - Previous involvement in audits or inspections. What we offer - Competitive salary and benefits. - Flexible working arrangements. - The opportunity to work closely with product development and quality teams on real regulatory deliverables. How to apply Please send your CV and a short cover letter describing your experience with technical files, quality systems, and regulatory submissions, to abbas.karladani@sunmedic.se. Mention any specific documentation or projects you have worked on.
Project Manager - Development
RaySearch develops innovative software solutions to improve cancer care. About 1000 clinics in more than 40 countries use RaySearch software to improve treatments and quality of life for patients. RaySearch was founded in 2000 and is listed on Nasdaq Stockholm. The headquarters is located in Stockholm, with subsidiaries in the US, Europe and Asia - Pacific. Today we are more than 400 employees with a common vision of improving cancer care with innovative software. Our great staff is crucial for our success and we offer a fantastic working environment in modern offices, flexibility and good opportunities for development. We believe in equal opportunities, value diversity and work actively to prevent discrimination. Do you have experience in project management and want to improve cancer care for patients around the world? Join RaySearch's development department as a project manager! About the position As a project manager at RaySearch you will be part of the team that is responsible for planning, leading and documenting product development projects, ensuring that we provide our customers with state-of-the-art oncology software. We work according to agile methodologies and with close collaboration between projects and departments within RaySearch. Responsibilities Plan the development projects and product releases together with fellow project management team members, collaborating both within the own project and across other projects and products Follow up project progress continuously together with the development teams Continuously work together with the development teams to improve processes and ways of working as well as to remove impediments Ensure that activities are performed, and documentation is produced according to our development process, including planning and participation in test management and risk management activities Communicate project status to relevant stakeholders Your profile We believe that you have a background in project management or experience from another leading role. To be successful in this position you should have a pragmatic approach to solving problems as they arise and be able to organize your work well. You enjoy facing new challenges and can find structure in a highly dynamic environment. We also believe that you have strong interpersonal and communication skills. You are capable of handling and prioritizing many requests and relations at once. You are used to working proactively and taking initiatives and you enjoy cross-functional collaboration and teamwork. Requirements: BSc or MSc degree in engineering, or equivalent 3+ years’ experience in project management within software development Previous experience of agile methodologies Excellent written and spoken communication skills (English and Swedish) Meriting: Experience from medtech industry or other regulated or safety critical industries Regulatory experience Experience working in Azure DevOps Server Our Culture Culture at RaySeach is the driving force behind our organization, where everything we do is driven by a shared passion for innovation and the fight against cancer. Our dedication is reflected in our ability to deliver exceptional results, pay close attention to detail, and consistently go the extra mile. Our employees stand out as experts in their field, driven by a relentless focus on solving problems - no matter how complex. At RaySearch, we take pride in leading the way in cancer treatment, leveraging cutting-edge technology to develop innovative solutions that make a real difference in patient care. Our Offer At RaySearch, we offer a diverse and inclusive work environment, fostering openness, sincerity, and collaboration. Located in Hagastaden, Stockholm's Life Science Hub, our modern and creative workspace includes an in-house gym, yoga, and social activities like ping pong, table football, and regular after-work events. Our bistro serves a fantastic lunch buffet, and we offer morning- and afternoon-fika every day. Our rooftop terrace also provides a stunning 360-degree view of Stockholm, enhancing the work experience. All of this comes attached with a competitive compensation and benefits package. Application Please apply for the position through the application form below. Selection and interviews will be ongoing. We do not accept applications by e-mail.
Senior Scientist, Product Science - Swedish Match
The role We are currently seeking a Senior Scientist to join the Product Science group, part of Swedish Match's Product Science & Research department in our R&D Center in Stockholm. In this role, you will generate scientifically grounded insights, contributing to building knowledge and understanding on nicotine and flavor performance for oral nicotine products, supporting decision-making across product development, study design, scientific strategy, and internal policy. You will do this by integrating data from multiple sources, applying your expertise in pharmacokinetics and statistics, and developing analytical workflows that are robust and easy to reproduce, all within a team that values collaboration and curiosity. You will lead and manage your own projects, but you will also work as a part of the cross-functional teams and support others by sharing your knowledge and expertise. You will collaborate closely with scientists and research teams across Swedish Match and PMI's global R&D organization. Key Responsibilities: Aggregates, analyzes, and interprets scientific data related to nicotine and flavor performance to support product development and scientific strategy. Analyze pharmacokinetic (PK) data and apply modeling tools, develop and maintain reproducible analytical workflows and statistical programming solutions. Supports the design and planning of human studies and consumer investigations, including administration, sampling strategies and endpoint analysis. Synthesize data from diverse sources, including scientific studies and publications, into actionable insights for cross-functional teams. Translate scientific findings into knowledge that guides product innovation/development and scientific strategy. Interpret and communicate complex scientific data to both scientific and non-scientific stakeholders. About you As a person, you have a high level of scientific curiosity and critical thinking, combined with the ability to manage multiple priorities and drive progress in scientific projects. In this role you will work both as SME in scientific research as well as being project responsible in collaborations across a global R&D organization. You enjoy working in a collaborative, cross-functional environment and are comfortable communicating complex scientific data to both scientific and non-scientific audiences. We value precision, initiative, and the ability to turn complex data into insights that support the business. Qualifications: Master's or PhD in Biostatistics, Pharmacokinetics, Pharmaceutical Sciences, Biomedical Engineering, or a related scientific field. Formal training in statistical modeling or pharmacometrics analysis is highly desirable. Minimum of 5 years of experience in a scientific role within pharmaceutical, biotech, or clinical research environments. Fluent in English, both spoken and written, is required. Proficiency in Swedish is considered a strong advantage. Requirements: Experience analyzing pharmacokinetic data. Experience in scientific programming and analytical workflow development. Proficiency in statistical programming (e.g. R, SAS). Experience with PK modeling tools. Strong understanding of study design, sampling strategies, and endpoint analysis, with experience working with large datasets. Ability to interpret, translate and communicate complex scientific data to cross-functional teams. Ability to manage multiple priorities and drive progress with minimal supervision. Ability to build effective partnerships and collaborations with internal and external partners. Highly developed communication skills, both verbally and in writing. Application: Please submit your application as soon as possible, but no later than 12 October. In this recruitment process, Swedish Match is collaborating with SallyQ. For questions about this position, please contact Ellinor Crafoord, Ellinor.crafoord@sallyq.se or Anna Tara Persson, annatara.persson@sallyq.se. About Swedish Match Swedish Match is an affiliate of Philip Morris International (PMI) and has been a leader in the industry for more than 200 years. Acquired by PMI in 2022, Swedish Match is at the forefront of transforming the industry - playing a key role in PMI's vision of delivering a smoke-free future. Product Science & Research is part of a global R&D organization with a dynamic and collaborative environment where people from various functions and teams come together to drive real change and shape the future of the industry.
Senior Principal Scientist Chromatography
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Senior Principal Scientist in Chromatography is responsible for scientific leadership in downstream purification. We are looking for a candidate with a strong application expertise in mAbs, Ab variants and other recombinant proteins, including process development expertise and biopharmaceutical manufacturing process understanding, with a deep understanding of chromatography fundamentals. This position reports to the Director for the Start to Finish Department in RnD, which is part of the Resins & Technologies Business Unit located in Uppsala, Sweden and will be an on-site role. The Start to Finish team focuses on application for customers complete end to end processes and thought leadership. What you will do: Support the organization as a chromatography Subject matter expert in Market Support and NPD projects. Actively work to identify and promote new business opportunities for Cytiva cross-functionally including but not limited to mAb (monoclonal antibody) and Ab (antibody) variants applications Drive innovation and strategy within the area of expertise. To take on responsibility as Project Manager for Research projects/Seed & Select activities if required Act as scientific/technology mentor for R&D personnel, not limited to the department. External visibility by presentations at external conferences and/or by publishing papers in scientific journals Actively contribute with product and customer expertise across the BioProcess organization Build and maintain an external network including biopharmaceutical companies, and initiate and lead external collaborations with customers and technology providers Build and maintain good knowledge of competitors and competing products/technologies If you are seeking a challenging role where your expertise in downstream processes and technologies as well as biopharma development can make a significant impact, we invite you to join our application team at Resins & Technologies. Let’s shape the future together. Who you are: PhD or equivalent experience At least 10 year experience of industrial development/R&D or scientific recognition At least 5 year experience as a Senior Scientist or equal High level external profile representing Bioprocess Proven record of scientific publications and/or IP Expertise in chromatography and protein purification with a deep understanding of chromatography fundamentals Strong communication skills Strong coaching and mentoring skills Executive presence, ability to communicate in a senior way with upper management Excellent English communication skills: Swedish is a plus To be successful in this role, we believe you demonstrate strong communication skills and the ability to convey ideas with clarity across all levels of the organization. You bring a thoughtful approach to supporting colleagues, sharing expertise and offering guidance when needed. With a strong executive presence, you engage effectively with senior leadership and contribute to strategic discussions. It would be a plus if you also possess previous experience in: The Biopharma industry. Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Regulatory Specialist
Welcome to SSC Space (formerly Swedish Space Corporation), the perfect workplace for those passionate about technology in general and space in particular. With space organizations, research institutes, institutional and commercial actors as customers, we offer specialist expertise in satellite communications, spacecraft consulting services, rocket and balloon systems, and much more. SSC Space also has one of the world's largest global networks of ground stations for satellite communications. We own and operate the Esrange Space Center in Kiruna, northern Sweden, with the aim of launching satellites in the near future. Are you ready to help shape the regulatory foundation for one of Europe's most exciting space initiatives? If you answer yes to this question, we invite you to seize the opportunity to make a significant impact as Regulatory Specialist within our Business Area Orbital Launch & Rocket Test. We are looking for a dedicated person who shares our core values of Customer Passion, Care, Collaboration, Curiosity and Courage. As Regulatory Specialist, you will join the team supporting the regulatory and licensing activities connected to SSC Space’s orbital launch ambitions and launch services. In this role, you will contribute to license applications, regulatory analysis and the continued development of processes for future launch operations. You will have the opportunity to develop your expertise within the team and gradually take on greater responsibility. We believe you have: A university degree in Law, Political Science, Public Administration, International Relations, European Studies or a related field. Up to three years of relevant professional experience, or have recently graduated with strong academic credentials and a clear interest in regulatory affairs. Excellent written and verbal communication skills in both Swedish and English. Strong analytical and documentation skills with the ability to translate complex requirements into practical actions and decision material. An interest in legislation, licensing, compliance and international regulatory frameworks. A structured, proactive and collaborative approach, with the ability to work independently while coordinating multiple stakeholders. Experience within aerospace, defence, export control, government authorities, compliance or other regulated industries is considered an advantage but is not required. In this role you will: Coordinate regulatory and licensing activities related to SSC Space orbital launch ambitions and launch services. Prepare, manage and follow up license applications for launch vehicles, payloads and associated space activities. Develop and establish regulatory processes, governance structures and compliance frameworks supporting future launch operations. Monitor, interpret and communicate national and international regulations affecting launch services, satellite operations, export control and related activities. Serve as SSC Space point of contact towards authorities, government agencies, industry stakeholders and international regulatory organizations. Support customers and internal stakeholders by providing guidance on licensing requirements and regulatory compliance throughout project lifecycles. We offer you A unique opportunity to contribute to a wide range of projects and play an active role in both the Swedish and international space industry. An excellent opportunity for personal and career development. An exciting, international workplace characterized by an open atmosphere and proud employees all over the world. Additional benefits In addition to vacation and traditional public holidays, we offer extra paid leave throughout the year, such as time off between Christmas and New Year and Ascension Day. Wellness allowance of SEK 5,000 per year. Health benefits such as voluntary health insurance and regular health checks for eligible employees. Access to a benefit bike through a tax-efficient leasing program. Support for employee-driven activities that promote connection, health and culture across teams. Collective Agreement, including attractive pension plans, parental pay and insurance. Location This is a full-time, permanent position based at Esrange Space Center in Kiruna or SSC Space Headquarters in Solna Further Information For questions regarding employment terms or union-related matters, you are welcome to contact our union representatives: Sveriges Ingenjörer: SverigesIngenjorer-AF@sscspace.com Unionen: unionen@sscspace.com Next Step If this opportunity sparks your interest, we encourage you to apply as soon as possible. We review applications continuously and will conduct interviews throughout the process. When applying, please include your CV. While you are welcome to include a brief personal note or letter, our evaluation will primarily focus on your skills and qualifications as outlined in your CV, ensuring a fair and unbiased recruitment process. This position requires approved pre-employment screening. These controls are based on the role that you will fulfill within the company. Due to the security and regulatory requirements associated with this position, applicants must hold citizenship in an EU member state. We help Earth benefit from Space SSC Space is a leading global provider of advanced space services, with more than 50 years of experience. We help space organizations, research institutes, commercial and institutional actors from all over the world to get access to space. With local presence on all continents and about 800 committed employees, we offer specialist expertise in satellite communications and satellite control services, spacecraft operations, rocket and balloon systems, launch services and flight test services, as well as engineering, operations and consultancy services for space missions. We help Earth benefit from Space. Learn more at sscspace.com.
Quality & Regulatory Manager
The Role Rarity Bioscience is looking for a hands-on Quality and Regulatory Manager to help transition our innovative molecular diagnostics technology from research use into clinical practice. This is a broad and operational role for someone who enjoys working close to both the science and the regulatory framework that enables products to reach patients. As part of a small Quality & Regulatory team, the successful candidate will take ownership of day-to-day quality and regulatory activities across the product lifecycle. The role spans both Regulatory Affairs and Quality Management, with responsibilities including supporting product development projects, maintaining technical documentation, handling interactions with Notified Bodies and authorities, overseeing post-market surveillance activities and ensuring compliance with applicable regulations and standards such as EU IVDR and ISO 13485. The position offers significant influence and visibility within the company. Working closely with Product Development, Product Management and Operations, the Quality and Regulatory Manager will act as a key business partner, helping shape regulatory strategy, support market access initiatives and ensure that quality and compliance considerations are integrated into decision-making. The position is based at our office in Uppsala. We work on-site at least three days per week and you will be part of a small Quality & Regulatory team, reporting to the Director of Operations, Quality & Regulatory. Duties & Responsibilities Represent Quality & Regulatory in new product development and product lifecycle management projects. Provide impact assessments for design, manufacturing, process and supplier changes. Prepare, review and maintain regulatory technical documentation, including documentation required under EU IVDR. Manage interactions with Notified Bodies and regulatory authorities, including submissions and change notifications. Participate in regulatory intelligence activities and monitor global regulatory requirements applicable to our products and operations. Review customer-facing materials, including data sheets, user manuals and website content, for accuracy and regulatory compliance. Represent the Quality & Regulatory function during internal and external audits. Contribute to market access activities supporting expansion into new markets, beginning with CE marking under EU IVDR. Conduct annual product dossier reviews and maintain post-market surveillance documentation. Support Quality Management System processes, including complaint handling, change control, CAPA, management review and audits. Drive the continuous improvement and effectiveness of the Quality Management System, ensuring compliance with ISO 13485 and applicable regulatory requirements. Your Profile The ideal candidate has several years of hands-on experience within the medical device or IVD industry, a practical understanding of quality and regulatory requirements, and the ability to translate regulations into workable solutions. Success in the role requires a proactive, self-driven and collaborative mindset, as well as the confidence to operate in a fast-moving scale-up environment where priorities evolve and individuals are expected to take ownership beyond their job description. Documented hands-on experience in medical device and/or IVD compliance management is a firm requirement for this role. Competencies & Areas of Expertise BSc degree or higher in life sciences, pharmacy, biomedical engineering, chemistry, or a related field. 5+ years of experience in a regulated medical device or IVD environment. Documented hands-on experience in regulatory affairs and/or quality management for medical devices or IVDs. Solid understanding of ISO 13485 and EU MDR/IVDR requirements. Professional proficiency in written and spoken English. It would be an advantage if you also have experience with: FDA regulatory requirements, including 21 CFR Part 820 and QMSR. Analytical reagent development and manufacturing. How to apply If this sounds like the right next step for you, submit your application. If you have questions about the role or the process, don't hesitate to reach out to Sandra Bydell Sveder at SallyQ (sandra.sveder@sallyq.se, 0763199688). About Rarity Bioscience Our superRCA® technology delivers unmatched sensitivity for detecting low-frequency mutations — enabling deeper insights into disease biology and earlier detection of relapse. A growing portfolio of superRCA kits is already in the hands of researchers and clinicians, with more on the way. We are about 30 people in Uppsala, working across functions without unnecessary layers. The culture is open, direct and prestige-free. Joining us means becoming part of a mission-driven team working to advance precision medicine through pioneering genetic analysis technologies, with the opportunity to make an impact on patients, healthcare and the future of molecular diagnostics.
Senior Product Compliance Coordinator - Malta
Come and join our journey! At Immense Group, we are guided by our core values of passion, boldness, and integrity. We strive to create an environment where our people thrive, driven by a love for innovation and a commitment to delivering exceptional player experiences. If you’re passionate about compliance and Product Operations, bold in your approach, and act with integrity, we’d love for you to join our team as a Senior Product Compliance Coordinator. A taste of what you’ll do The Senior Product Compliance Coordinator is responsible for leading the operational compliance function within Product Operations, ensuring all games and operational activities comply with regulatory requirements across all brands and jurisdictions. The role combines regulatory compliance with process governance, documentation, audit readiness, and continuous improvement while working closely with Product Operations, Legal & Compliance, DEVS, Projects, Partnership Management, and external providers. A key responsibility of the role is ensuring compliance processes, certifications, regulatory documentation, and operational controls remain accurate, audit-ready, and continuously improved to support operational consistency, regulatory compliance, and business growth. Regulatory Compliance & Operational Governance Lead the certification lifecycle, ensuring game certifications, re-certifications, and market-specific regulatory documentation remain accurate and up to date. Ensure games, promotions, configurations, and operational activities comply with jurisdictional and regulatory requirements before release. Coordinate regulatory documentation with Compliance, DEVS, Projects, testing laboratories, and game providers. Maintain certification repositories, compliance trackers, regulatory evidence, and audit documentation. Monitor regulatory changes and coordinate operational implementation across Product Operations. Support internal and external audits by preparing documentation, coordinating evidence, and following up on audit actions. Create, maintain, and continuously improve compliance procedures, SOPs, checklists, and regulatory documentation. Ensure compliance documentation remains accurate, current, and aligned with regulatory requirements and operational workflows. Support the development of compliance-related Knowledge Base articles and onboarding material. Promote standardisation of compliance processes across Product Operations. Prepare compliance reports, certification trackers, regulatory dashboards, and market-specific reporting. Identify compliance risks, operational gaps, and opportunities to strengthen operational controls. Support implementation of automation initiatives and AI-assisted tools that improve compliance processes, documentation, and reporting. Work closely with Product Operations, Legal & Compliance, DEVS, CRM, Customer Operations, Projects, and external providers to maintain regulatory alignment. Participate in operational, regulatory, and cross-functional projects as required. Support new market launches and regulatory initiatives. Maintain sufficient operational knowledge to provide support across Product Operations where required and contribute to business continuity. Perform any other task or responsibility related or connected to the role. Additional Responsibilities Reporting, Improvement & Coordination Audit Readiness & Compliance Documentation Who and what we are after? Minimum of 3 years’ experience within the iGaming industry in Compliance, Product Operations, Certification Management, QA, or a similar operational role. Demonstrated experience managing regulatory documentation, certifications, audits, or compliance-related processes. Good understanding of casino games, game certifications, regulated markets, and operational compliance requirements. Strong analytical and problem-solving skills, with the ability to identify compliance risks and recommend practical solutions. Excellent attention to detail and organisational skills. Experience developing or maintaining compliance documentation, SOPs, checklists, and regulatory procedures. Experience supporting or leading process improvement and operational governance initiatives. Comfortable working with compliance reports, certification trackers, regulatory dashboards, and operational metrics. An interest in automation and AI-assisted operational processes. Excellent written and verbal communication skills in English. Strong stakeholder management skills and the ability to work effectively across multiple teams. Ability to manage multiple priorities in a fast-paced and regulated environment. Strong sense of ownership, accountability, and operational discipline. Ability to work collaboratively as part of a team while also working independently and taking ownership of allocated responsibilities. Employee benefits Private health insurance – because your wellbeing matters to us Wellness allowance – up to €300 per year Fresh and healthy breakfast and lunch prepared every day in our penthouse kitchen – you can save up to €3,000 a year Birthday leave – as we want you to celebrate your day Company and team-building events – trust us, these are legendary Relocation package to Malta, including a flight and two weeks of accommodation And much more – see for yourself! Apply today and be part of our success story!
Senior Regulatory Affairs Manager - Camurus (Lund)
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. At Camurus you will get the opportunity to work with committed colleagues in a fantastic Regulatory Affairs team with good atmosphere and supportive colleagues. Camurus is an innovative company currently expanding and establishing in new markets. In this position you will be part of the Regulatory team, based at the headquarters in Lund. The team today consists of 15 colleagues working with regulatory affairs activities, covering all existing and potential Camurus markets. You will work in a deadline-driven and international environment requiring a high level of flexibility. This is a key position where you will support marketed products. You will get the chance to work with different markets like EU and rest of the world. You will lead critical regulatory activities, ensuring compliance and facilitating effective communication with health authorities. You will be expected to quickly become a working part of the team. Your responsibility: · Lifecycle and maintenance activities for marketed products. · Maintaining core labelling, preparing and maintaining local labelling. · Contributing to and leading health authority interactions. · Monitoring regulatory intelligence information on a regular basis. · Represent Regulatory Affairs (RA) in the cross-functional teams and drive the regulatory agenda, raise RA concerns and opportunities. Candidate profile We are looking for a candidate with at least 10 years professional pharma industry experience, and at least 5 years regulatory affairs experience, preferably from a global RA team working with US and EU markets. This means you have good understanding of relevant regulatory-related regulations and guidelines. You have a Bachelor or Master of Science degree. Excellent communication and documentation skills (oral/written) in English is required, together with project management skills. To be successful in this role, you need a structured and organised mindset with strong focus on details and time management. You are good at independently managing multiple ongoing projects, but at the same time you enjoy working in a team. Even though you are highly structured, you support change and can adapt to new conditions. We value a supportive and flexible “roll up the sleeves” attitude. You see solutions rather than problems and you possess a strong personal drive. We also believe you have the “maintenance mindset”, crucial for working with products already on the market. Camurus offers This is a great time to join a highly dynamic company during an exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market - and the ambitions are to continue in the same way. With a diversified project portfolio in different stages, the commercial potential is considerable. This position offers a fantastic opportunity to work in a competent and committed Regulatory team – where the laughter is never far away. Camurus has 300 employees with the headquarters located in Lund. The corporate culture is driven by the core values of innovation, collaboration, ownership, quality, and passion for realizing a 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: www.camurus.com/. We are looking forward to seeing your application!
Regulatory Affairs Specialist
About the Role As a Global Regulatory Specialist, you will join our Quality & Regulatory Affairs team to help ensure our medical devices and mounting systems meet global regulatory requirements. Please note: This is a hybrid role with 1–3 days per week onsite at our Stockholm office in Östermalm, especially during onboarding. Occasional international travel (10–20%) may be required and will be communicated in advance. In this role you will: Streamline regulatory processes and set a roadmap in collaboration Product & Development, QA, and Operations teams. Coordinate with internal and external auditors to support audit readiness. Review device classifications and regulatory challenges across markets. Maintain and update technical documentation (Annex II & III) and declarations of conformity, including EU Declaration of Conformity, in alignment with the associated technical documentation. Coordinate establishment of registrations and device listings with the FDA, Authorized Representatives, and Importers/Distributors. Support product registrations and market access activities (EU MDR Class I, FDA 510(k)-exempt Class II). Monitor regulatory changes and communicate implications to relevant teams. What We’re Looking For We are looking for a structured and collaborative regulatory professional who enjoys solving problems with a logical approach, works autonomously while contributing to strategic initiatives, and thrives in a dynamic, cross-functional environment. We’re looking for a detail-oriented and analytical professional with: A bachelor’s degree in Regulatory Affairs, Life Sciences, Electrical-Electronics or a related field. At least 5 years of experience in medical device regulatory affairs with hands-on experience with EU MDR (Class I) and FDA QSR. Experience with regulatory systems, document control tools, and QMS platforms and exposure to technical documentation, internal and external audits for regulatory compliance Strong organization, coordination and communication skills to engage auditors and communicating with stakeholders across functions and levels. Ability to break down complex regulatory topics clearly for both technical and non-technical stakeholders. Proficiency in both spoken and written communication in English. Ideal candidates will bring: Familiarity with embedded systems and experience with IEC 62304. Experience with EU MDR (Class II/III).
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