Study Advisor in Odia
Our vision is to become Sweden's best school municipality. Sollentuna's municipal schools achieve strong student results and have high safety ratings thanks to fantastic employees. By using research and proven pedagogical methods, we aim for even higher quality to stimulate children's and young people's creativity and learning. In our schools, students should achieve excellent academic results and develop the skills and abilities required for future studies and professional life. The Center for Integration and Multilingualism (CIFS) is responsible for native language instruction and study guidance in Sollentuna municipality's primary schools. We operate from newly renovated premises in Turebergshuset, in the heart of Sollentuna Centrum, but our most important arena is meeting with students. At CIFS, you become part of a professional and engaged workplace where we put the student at the center. By strengthening students' native language and cultural identity, we give them keys to increased self-confidence and a deeper understanding of the world. Responsibilities We are now looking for a study advisor in Odia for a 10% position. This is a fixed-term employment contract for 1 year. Remote work is possible. Provide study guidance in various primary school subjects. Plan study guidance in collaboration with the student's subject teacher. Conduct study guidance in various primary school subjects based on the student's capabilities and needs. Actively participate in CIFS team meetings and collaborative learning. In our team, you will meet experienced and supportive colleagues, close leadership, and a clear structure with regular meetings and professional development. Here your expertise is important to help students find security, joy, and pride in their language. Qualifications As a person, you have strong pedagogical insight and meet students and guardians with a professional and confident approach. You have good knowledge of various primary school subjects and a strong ability to collaborate and build good relationships. Requirements Very good proficiency in Odia (native speaker level). Pedagogical education. Experience teaching children and/or young people. Ability to communicate in Swedish. Strong digital skills. Merits Teacher certification. Experience using digital tools in teaching. In this recruitment, we place great importance on personal suitability. Background checks from the police register will be conducted before employment. Interviews are conducted on a rolling basis; please submit your application today. What We Offer Welcome to Sollentuna – a municipality full of possibilities! Together we make Sollentuna better every day for our residents, entrepreneurs, and organizations. We have clear and ambitious goals to create security, welfare, and sustainable growth. We offer you a meaningful and enjoyable job in a stable environment where ambition levels are high. With us, you get fantastic colleagues who want to make a difference for others. We are now looking for someone who is innovative, responsible, and welcoming. Join us on the journey to create Sweden's most attractive municipality!
Swedish Motorsports Association (Svenska Bilsportförbundet) is seeking a Chief Financial Officer (CFO)
Do you want to be part of shaping the future finances of one of Sweden's largest specialized sports federations? Swedish Motorsports Association is in an exciting development phase where financial management, long-term sustainability, and strategic leadership are crucial for our continued growth. We are therefore seeking a Chief Financial Officer (CFO) who wants to be a key person in our management team and contribute to developing Swedish Motorsports for the future. This is a role for you if you want to combine qualified financial responsibility with strategic financial work in an organization where social benefit, member benefit, and business efficiency go hand in hand. Swedish Motorsports Association operates extensive activities with financing from member fees, commercial partnerships, subsidiary operations, as well as national and international development projects. To continue developing Swedish Motorsports, we are now seeking a CFO who sees finance as a strategic tool for growth, sustainability, and member benefit. About the Role As CFO, you have overall responsibility for Swedish Motorsports Association's financial management and financial development. The role is significantly broader than traditional financial administration and means you are a partner to the Secretary General, management team, and Federation Board. You are responsible for creating financial conditions that enable a long-term sustainable federation with high transparency, good internal control, and well-founded decision-making documentation. The position may include assignments and financial responsibility for subsidiaries that are wholly or partially owned by Swedish Motorsports Association. We are not just seeking a financial administrator – we are seeking a strategic financial leader. A person who wants to be part of developing Swedish Motorsports Association's future financial conditions, create long-term financial stability, and contribute to Swedish motorsports continuing to grow through good governance, sustainable financing, and close collaboration with both member organizations and national and international partners. Your Main Areas of Responsibility In your role as CFO, you will, among other things: • Lead and further develop Swedish Motorsports Association's financial management • Be responsible for budget processes, business planning, forecasts, and financial monitoring • Ensure quality in ongoing accounting, financial statements, annual reports, and other financial reporting • Develop internal control systems, management models, and financial processes • Be responsible for liquidity planning, financing, and financial risk management • Identify and analyze financial risks and propose measures • Ensure compliance with legislation, accounting regulations, tax rules, and grant conditions • Prepare qualified decision-making documentation for investments, organizational changes, and other strategic decisions • Develop financial analyses, key performance indicators, and monitoring models that strengthen organizational management • Coordinate financial matters between the federation and its subsidiaries as well as external partners • Be responsible for financial management, monitoring, and quality assurance of projects financed through, among others, Swedish Sports Confederation (RF), Fédération Internationale de l'Automobile (FIA), public grants, and other national and international funders • Ensure that conditions for grants, project funds, and external financing are met and develop procedures for effective monitoring and reporting • Contribute to identifying and developing new financing opportunities through projects, development funds, and external partnerships We Are Looking for You We seek a confident and experienced financial leader with a genuine interest in business development and financial management. We would like to see that you have experience in financial management within organizations where external financing, project funds, and grant-financed activities form an important part of the organization's long-term development. We believe you have: • An academic degree in finance/economics • Several years of experience in qualified financial leadership, preferably as a CFO or similar position • Excellent knowledge of financial management, accounting, budgeting, financing, and internal control • Experience working strategically with business development • Strong knowledge of Swedish accounting and relevant legislation • Strong English language skills, both spoken and written Meritorious Experience It is particularly meritorious if you have experience with: • Work within the sports movement or other member-governed organization • Finance in organizations with both non-profit operations, federation operations, and corporations • Publicly financed activities and grant management • Group-like financial structures or multiple legal entities • Financial management, reporting, and monitoring of projects financed by, for example, Swedish Sports Confederation (RF), FIA, EU programs, or other national and international funders • Working with grant-financed activities and development projects Personal Qualities To succeed in this role, we believe you are: • Analytical and future-oriented • Structured with high integrity • Unpretentious and collaboration-oriented • Communicative and pedagogical • Confident in making decisions and building trust in complex organizations What We Offer At Swedish Motorsports Association, you have the opportunity to work in an organization with strong commitment, high ambitions, and an important role in Swedish sports. You will become part of the management team and have an active influence over the federation's continued development. Here you have the opportunity to combine strategic leadership with work that contributes to Swedish motorsports' future. Location Swedish Motorsports Association, Bergkällavägen 31 A, Sollentuna Contact Person: Mikael Johansson, Secretary General, [email protected] The position is a permanent full-time employment (a 6-month probation period may be used). Application Please send your application with CV and cover letter to: [email protected] The application deadline is September 30, 2026. Selection and interviews will be conducted on an ongoing basis, so we would appreciate if you submit your application as soon as possible. Position start date January 1, 2027 or by agreement (earlier or later). References should be provided with the application. Swedish Motorsports Association declines all offers of advertising and recruitment assistance in connection with this announcement.
Preschool Teacher - Smultronställets förskola
Our vision is to become Sweden's best school municipality. Sollentuna's municipal preschools maintain high quality and satisfied parents thanks to fantastic staff members. Here you'll work in an environment where children's curiosity and your professional drive have space to flourish. We work long-term on pedagogical development, modern learning environments, and strong collegial learning. With us, you'll have room to grow and the opportunity to make a real difference every day. Smultronställets is centrally located in Häggvik, with close proximity to commuter trains and several schools. Our lush yard invites movement, play, and encounters. Here children cultivate vegetables and flowers in garden boxes and explore different forms of expression in our outdoor atelier. We work inspired by the Reggio Emilia philosophy, where democracy, belief in the competent child, active co-researching educators, multilingualism, pedagogical documentation, and exploratory learning environments are central elements. Our operations include both a pedagogista and an atelierista. Job Responsibilities As a preschool teacher at Smultronställets förskola, you have a central role in pedagogical work with focus on children's curiosity, learning, and development. Through a project-based and exploratory approach, you utilize children's thoughts, ideas, and questions and stimulate their development through play, creativity, and various learning processes. The position includes planning, implementing, documenting, following up, and developing education together with the team. You work according to the facility's operating hours, which includes both openings and closings. You actively work with language development and communication to give all children the opportunity to express themselves and participate according to their own abilities. As a preschool teacher, you are a democratic leader who builds positive relationships with children, parents, and colleagues and contributes to an open work climate. With an attentive and respectful approach, you see each child's feelings and needs and contribute to an operation where differences are seen as an asset. You work to ensure children feel secure, develop independence, and strengthen confidence in their own abilities. Qualifications We're looking for someone who has an ease for creating and developing trusting relationships with children, parents, and colleagues. You enjoy collaborating and actively contribute to a positive work climate where you drive operations forward together. Through your pedagogical insight, you can translate ideas and knowledge into practice and create conditions for children's learning, development, and participation. You are confident in your professional role, take responsibility for your assignment, and act with judgment and personal maturity. At the same time, you are flexible and have an ease for adapting to the facility's needs and conditions. Requirements Licensed preschool teacher Previous work experience from preschool Meritorious Experience working with inspiration from Reggio Emilia In this recruitment, we place great emphasis on personal suitability. Prior to employment, a criminal record check will be conducted. Interviews will be held on-site at Turebergshuset in the morning on October 8. We Offer Welcome to Sollentuna – a municipality in the heart of possibilities! Together we make Sollentuna better every day for our residents, entrepreneurs, and organizations. We have clear and ambitious goals to create security, welfare, and sustainable growth. We offer you a meaningful and enjoyable job in a stable environment where ambition levels are high. With us, you'll find fantastic colleagues who want to make a difference for others. Now we're looking for someone who is innovative, responsible, and welcoming. Join us on the journey toward creating Sweden's most attractive municipality!
Park Worker for Planting Areas at Street/Park in Upplands Väsby Municipality
We are now seeking a Park Worker with special responsibility for planting areas at Street/Park in Upplands Väsby Municipality! Do you have a background in horticulture or similar? Are you responsible and solution-oriented? Do you enjoy working outdoors? Then do not hesitate to apply for this position! What We Offer You We offer you an opportunity to work in an inspiring environment where you contribute to beautifying our municipal outdoor spaces! As a Park Worker with special responsibility for planting areas, you will become part of a competent team that values quality and creativity. Here are some of the benefits you can look forward to: Development Opportunities: We believe in investing in our personnel and offer training to strengthen your skills and knowledge in green space management. A Positive Work Environment: Our team is characterized by collaboration and community, where we support and encourage each other in our work. Attractive Benefits: As part of our team, you will have access to competitive salaries and benefits that promote your health and well-being. Meaningful Work: You will have the opportunity to see the results of your work in the form of beautiful and blooming parks that everyone can enjoy year-round. Come and Make a Difference With Us! About Us We are a work group passionate about creating and maintaining green, lively, and well-maintained outdoor environments. With a focus on sustainability and aesthetics, we strive to make our outdoor spaces attractive places where people can enjoy and socialize. As part of our team as a Park Worker with special responsibility for planting areas, you will play a central role in our vision of developing outdoor environments that flourish and thrive. We value teamwork and community, and believe in creating a work environment where everyone can contribute their ideas and experiences. Together, we work to maintain high quality in our work, which enables us to provide visitors with a fine experience in our parks. With us, you have the chance to grow and develop in your role while working to make a difference in your community. If you share our passion for horticulture and enjoy working outdoors, we look forward to hearing from you! About the Position As a park worker with special responsibility for planting areas, you will work with the maintenance and upkeep of our parks, plantings, and green spaces. The work is varied and follows the changes of the seasons. You will work both independently and together with colleagues to ensure that our outdoor environments maintain high quality. Other tasks such as spring cleaning, leaf collection, and grass cutting may occur. In winter, you are part of the winter operations with snow and ice management. Work Tasks Maintenance and upkeep of planting areas Planting and establishment of plant material Weed removal, fertilizing, and watering Pruning and maintenance of shrubs and trees Maintenance of grass areas and lawns Participation in the development and improvement of our green environments Handling of machines and tools used in park operations Are You the One We're Looking For? We are seeking you who have: Horticultural training or other education/experience that we consider equivalent Good plant knowledge and knowledge of plant care and development Experience with maintenance and upkeep of planting areas, shrubs, trees, and grass areas Ability to work independently and take responsibility for your work tasks Class B driver's license Good Swedish language skills, both spoken and written It is a merit if you have: Experience with maintenance of public or public outdoor environments Good machinery experience and experience with park and garden machinery Brush cutter license Chainsaw license Vocational certificate in pruning and tree care Experience in municipal park management or similar operations As a Person To succeed in the role, you are structured and confident in your work, with the ability to plan and take responsibility for your work tasks. You are creative and see opportunities to develop our planting areas and green environments. As a collaboration-oriented person, you contribute to a good work climate and enjoy working both independently and together with others. If you also enjoy working outdoors and have a sense for nature's beauty, you will fit perfectly into our team. Do not hesitate to apply – we look forward to welcoming you to our community and creating fantastic outdoor environments together! Warmly Welcome Your Application! We only accept applications through our recruitment system. Background checks may occur during the recruitment process. Read more about our offices and workplaces: Municipality's Workplaces Meet some of our employees: Meet Our Employees With us, you receive both secure employment terms and several different employee benefits, including a wellness allowance and favorable offers through our benefits portal. More information can be found at: The Municipality as Employer Upplands Väsby Municipality is a Swedish-speaking administrative area, so please inform us if you are a Finnish speaker. Open to All We focus on your skills, not your other circumstances. We are open to adapting the role or workplace to your needs.
Temporary Radiology Technologist at Löwenströmska Hospital
Unilabs is one of Europe's leading diagnostic companies offering services in laboratory medicine, pathology, genetics, radiology, and mammography. Our role is to find the best diagnostic solutions for safe and efficient healthcare. At Unilabs, every employee contributes to our collective ability to help more people achieve longer and healthier lives. We see this as a great responsibility and a fantastic privilege – because we know that every diagnostic examination makes a difference. We are now seeking an engaged radiology technologist interested in working on a temporary basis with us at Unilabs at Löwenströmska Hospital in Upplands Väsby! Your role as a radiology technologist We welcome you to our excellent team at Löwenströmska Hospital where we offer examinations in MR, CR, CT, and US. As a temporary radiology technologist with us, you will have the opportunity to work with short notice and cover shifts as needed. Work may also include longer continuous periods, depending on operational needs. The position is hourly paid with a focus on daytime shifts and employment starts according to agreement. What we value in you At Unilabs, attitude is as important as competence. Therefore, we are looking for someone who is engaged, flexible, and meticulous in their work. You have an open-minded approach, are solution-focused, and enjoy collaborating with others. We also see that you are attentive, communicative, and have a strong service orientation when meeting colleagues, patients, and healthcare providers. We are looking for someone who: Is a licensed radiology technologist Has good knowledge of Swedish in speech and writing It is a great plus if you have previous work experience in this role and experience working with conventional radiography, CT, and/or MR. We work at the heart of healthcare Unilabs is one of Europe's largest diagnostic companies and one of the few offering laboratory medicine, imaging diagnostics, and pathology within the same group. With us, there is therefore enormous collective expertise around the questions that are among the most important for us and our health. Our culture is characterized by care where CARE BIG is a mantra that runs through everything we do. We don't just work with tests and samples – we work on improving people's lives. Curious about becoming part of our team? Then you are warmly welcome to submit an application, or recommend someone you think would be a good fit. We review applications on an ongoing basis and the position may therefore be filled before the final application deadline. If you have questions, please feel free to contact recruiting manager Ann-Charlotte Lindevall, [email protected]. We look forward to meeting you! Unilabs is one of Europe's leading diagnostic companies and Sweden's largest private provider of radiography, mammography, and laboratory medicine. We meet patients and customers at hospitals, urgent care centers, primary care laboratories, and at our own radiology units and clinics. In Sweden we have just over 1,300 employees and together with our colleagues in Europe we number over 11,500. Our largest professional groups are biomedical analysts, radiology technologists, and physicians with specialist competence in radiology and laboratory medicine. Together we work to ensure high-quality diagnostics, which form the basis for important treatment decisions every day. Want to get to know us better? Feel free to read more about us at www.Unilabs.se and follow us on LinkedIn!
Edsbergsskolan Seeks Assistant Principal for Adapted Elementary School
Do you want to be part of developing a school where student safety, learning, and future are at the center? We are now seeking an engaged Assistant Principal for Edsbergsskolan's adapted elementary school. Edsbergsskolan is a middle school with the vision "safe students who thrive in school and are well prepared for the future". The school consists of two operations: elementary school for grades 7–9 with nearly 300 students and adapted elementary school for grades 7–9 with approximately 30 students. We offer specialization in music and sports as well as advanced education in English and mathematics. Edsbergsskolan has among the highest employee satisfaction scores in the municipality and is characterized by a positive work climate, high participation, and great opportunities to influence the development of the operations. Here you will meet a student body that reflects society's diversity and a school that continues to develop forward. Responsibilities As Assistant Principal, you are responsible for leadership and development of the adapted elementary school and its short-term supervision. You have delegated responsibility for operations, staff, and students, and you work to create the best conditions for student learning, development, and well-being. In this role, you are also responsible for work with students in need of special support within both the adapted elementary school and the elementary school. Through your special education and behavioral analysis expertise, you contribute to developing the school's inclusive learning environments and strengthen the operation's ability to meet students' diverse needs. You drive systematic quality work with a focus on developing, monitoring, and improving the operations. Together with the school's Assistant Principal for the elementary school, three team leaders, and a representative from student health services, you are part of the school's leadership team led by the Principal. Qualifications We are looking for someone with experience in school leadership within adapted elementary school and special education training. It is an advantage if you have started or completed the state principal training program. We would like to see that you have experience working with students with various neuropsychiatric disabilities (NPF). Experience and training in behavioral analysis is also considered an advantage. To succeed, we also see that you have: Good understanding of intellectual disability (IF) and the pedagogical consequences that various disabilities can have. Experience in student health services and in collaborating around students in need of special support. Experience in analyzing, developing, and adapting learning environments based on students' individual needs. Experience in preventing and managing problem-causing behaviors through structured, evidence-based, and pedagogical approaches. As a person, you are confident, clear, and structured. At the same time, you are flexible and open to change as work tasks can change relatively quickly based on student and operational needs. You have a relationship-building leadership style, are persistent in your development work, and have the ability to create engagement and participation among both staff, students, and guardians. We place great emphasis on personal suitability. Before employment, a background check register statement is conducted for work in the school system. Welcome to Sollentuna – a municipality in the middle of possibilities! Together we make Sollentuna better every day for our residents, entrepreneurs, and organizations. We have clear and ambitious goals to create safety, welfare, and sustainable growth. We offer you a meaningful and enjoyable job in a stable environment where the level of ambition is high. With us you get fantastic colleagues who want to make a difference for others. We are now looking for you who is innovative, responsible, and welcoming. Join us on the journey toward creating Sweden's most attractive municipality! Open to All We focus on your skills, not your other circumstances. We are open to adapting the role or workplace to your needs.
Program Director at Rudbeck in Sollentuna
Do you want to work in the heart of opportunity and lead one of Sweden's largest upper secondary schools into the future? Rudbeck is now seeking an engaged and courageous educational leader who wants to take responsibility for two of our technology-intensive programs and drive school development together with colleagues, students, and parents. Rudbeck is Sollentuna municipality's municipal upper secondary school and is located next to Edsviken and the beautiful Edsbergsparken, two miles north of Stockholm. The school has approximately 2,400 students and around 250 employees. We offer a broad range of programs and specializations which contribute to fantastic diversity, making Rudbeck one of the Greater Stockholm area's most popular upper secondary schools. Job Description As a Program Director at Rudbeck, you will be responsible for the Technology Program as well as the Electrical and Energy Program. Your task is to lead and coordinate the educational work with a focus on high goal achievement and continuous development. You are responsible for personnel, budget, and work environment within your area, according to delegation. In close collaboration with other principals and the school director, you plan, follow up, and evaluate instruction and drive systematic quality work. You represent the operation as a whole in various contexts and build trusting relationships with students, colleagues, parents, union representatives, and other stakeholders. Qualifications We are looking for someone with experience as a principal, preferably in upper secondary school, or many years of experience as an assistant principal at the upper secondary level. You have teacher training or other equivalent pedagogical education as well as a degree from the state principal training program. You are an engaged and courageous educational leader with the ability to inspire and motivate both colleagues and students. As a leader, you are clear and results-oriented, and you direct the operation in accordance with national and municipal goals as well as the school's governing documents. We see that you have experience with school development and leading in change processes, as well as experience working strategically to improve the school's pedagogical activities. You have very strong collaboration skills, particularly in working with other program directors, and you promote a culture characterized by collegial learning and collaboration based on professional experience and current research. You have well-developed communication skills in both speech and writing, as well as good digital competence. Application In addition to your formal qualifications, great emphasis is also placed on your personal competencies. If you are seeking a new and qualified challenge and feel that you fit the description, you are warmly welcome to submit your application. This position is a permanent full-time employment with a start date to be agreed upon. A background check will be conducted prior to hiring. For questions, contact Recruitment Director Björn Kullgard. Union contacts can be reached through Sollentuna municipality's contact center 08-579 210 00 We Offer Welcome to Sollentuna – a municipality in the heart of opportunity! Together, we make Sollentuna better every day for our residents, entrepreneurs, and organizations. We have clear and ambitious goals to create safety, welfare, and sustainable growth. We offer you a meaningful and enjoyable job in a stable environment where the level of ambition is high. With us, you get fantastic colleagues who want to make a difference for others. Now we are looking for you who are innovative, responsible, and welcoming. Join us on our journey toward creating Sweden's most attractive municipality! Open to All We focus on your competence, not your other circumstances. We are open to adapting the role or workplace to meet your needs.
Project Manager - Lead Reform Work in Preschool, Primary School, and Upper Secondary School
Project Manager - Lead Reform Work in Preschool, Primary School, and Upper Secondary School Are you an experienced principal or school leader with the ability to lead change, provide direction, and translate national reforms into concrete development across preschool, primary school, upper secondary school and adapted school forms, as well as other activities regulated by the Education Act, such as the municipality's activity responsibility. Job Responsibilities As a project manager, you will have a key role in the Department of Children and Education's strategic development work. The assignment involves creating structure, coordination, and momentum in work with the reforms and changes that affect preschool, primary school, and upper secondary school. You will work closely with the school director, administrative management, and principals to translate national reforms, investigations, and updated steering documents into concrete priorities, approaches, and initiatives in the operations. In this role, you are responsible for analyzing new requirements and steering signals, identifying what consequences they have for the organization, leadership, teaching, skills provision, and resource use, and ensuring that the change work is conducted in a coordinated and long-term manner. You drive development processes together with principals and other key functions, develop decision-making materials, and contribute to translating ideas, ambitions, and political goals into practical action with a focus on increased quality and improved results for children and students. An important part of the assignment is to coordinate work between the municipality's different school forms and create a common thread in the education strategy. By monitoring external developments and identifying upcoming changes, you contribute to the municipality staying ahead in the development of educational activities. You also follow up on the effects of implemented measures, identify obstacles, and adjust approaches and priorities as needed to ensure that the development work achieves the desired results. The assignment is conducted during the school years 2026/2027 and 2027/2028, with the possibility of extension. The employment is a project position. Qualifications We are looking for someone with substantial experience leading and developing educational activities at the principal level, for example as a principal or other qualified school leadership position. You have documented experience driving change and development work in schools and are accustomed to translating political decisions, national reforms, and steering signals into implementable initiatives that create results in the operations. To succeed in this role, you need to have: A very good understanding of how national reforms impact preschool, primary school, and upper secondary school, and can analyze complex issues from both a strategic and an operationally-focused perspective. A structured approach in which you identify priorities, clarify choices, and translate analyses into concrete actions that create momentum. The ability to provide direction, engagement, and drive even in situations where the change is extensive or presents new requirements for the organization. The ability to produce clear and target-group-adapted written materials, reports, and presentations that summarize complex issues, highlight analyses, and support dialogue, decision-making, and continued work. Be a skilled communicator who builds trusting relationships and collaborates effectively with different stakeholders. As a person, you are driven, results-oriented, and have the integrity to raise issues that need to be changed. You combine a strategic perspective with a good understanding of the day-to-day operations and have the ability to switch between long-term development issues and operational problem-solving. You have a strong commitment to children's and students' learning and want to be part of developing the municipality's educational activities for the future. The employment requires a passed background check and extract from the criminal register. The position is filled subject to the required decisions being made. WE OFFER Welcome to Sollentuna – a municipality in the midst of possibilities! Together we make Sollentuna better every day for our residents, entrepreneurs, and organizations. We have clear and ambitious goals to create safety, welfare, and sustainable growth. We offer you a meaningful and enjoyable job in a stable environment where the level of ambition is high. With us, you get fantastic colleagues who want to make a difference for others. Now we are looking for someone who is innovative, responsible, and welcoming. Join us on the journey toward creating Sweden's most attractive municipality! Open to Everyone We focus on your qualifications, not your other circumstances. We are open to adapting the role or workplace to your needs.
Recreation Leader – Edsbergs Fritidsgård
We are now hiring dedicated recreation leaders for one of our youth centers that creates safety, community, and meaningful activities for young people ages 13–17. With us, you will work closely with youth, build relationships, and develop activities where participation is in focus. You have a good understanding of the importance of leisure time in young people's lives and development. The role includes collaboration with schools, social services, police, and civil society organizations. This requires strong collaboration skills, clear role understanding, and a professional approach. Qualifications Experience working with young people, preferably in vulnerable areas Knowledge of pedagogical methods that promote participation Experience in activity-based youth recreation leadership Recreation leader training or other education that the employer deems equivalent We are looking for someone who has drive, initiative, and genuine curiosity. You are confident in yourself, open in your interactions with others, and have a talent for building trusting relationships. You are skilled at networking and collaborating with actors such as police, schools, social services, and youth organizations. You see possibilities, have a positive attitude, and actively contribute to a safe and developmental environment for young people. You work in a structured manner, can plan and follow up on activities, and enjoy leading youth-driven projects and forums for influence. You have experience in collaboration both internally and externally. Additional Requirements and Information Good ability to express yourself well in speech and writing in Swedish Evening and weekend shifts are included For this position, a background check and a check of the Police Records Register will be conducted The Youth Department of Sollentuna operates youth centers and safety centers for children and young people ages 7–17. We work in a needs-driven and knowledge-based manner with a focus on safety, development, and meaningful activities. The municipality's goal is that no areas should be classified as vulnerable by 2030, which makes collaboration and safety-creating work central parts of our operations. Welcome to Sollentuna – a municipality in the middle of opportunities! Together we make Sollentuna better every day for our residents, entrepreneurs, and organizations. We have clear and ambitious goals to create safety, welfare, and sustainable growth. We offer you a meaningful and enjoyable job in a stable environment where ambition levels are high. With us, you will have fantastic colleagues who want to make a difference for others. We are now looking for someone who is innovative, responsible, and welcoming. Join us on the journey toward creating Sweden's most attractive municipality!
LSS Case Officer for Adults at the Care and Social Services Office in Sollentuna
Do you want to work in an organization where quality, collaboration, and people's self-determination are at the center? Are you looking for a position where you can make a real difference while receiving strong support from experienced colleagues and managers? Then you might be the person we're looking for. We are now welcoming an engaged and professional LSS case officer for adults to the Disability Services Division at the Care and Social Services Office in Sollentuna Municipality. Job Description As an LSS case officer, you meet adults with various disabilities and life situations. Through qualified public administration, you contribute to helping people get the support they need to live an independent and meaningful life. You are responsible for investigating, assessing, making decisions, and following up on interventions according to LSS, the Social Services Act (SoL), and the Riksfärdtjänst Act. The work involves many points of contact and close cooperation with individuals, relatives, service providers, and other partners. With us, you work independently while always having colleagues to consult with. We believe in developing together and offer a working environment where knowledge, humility, and care characterize the daily work. Qualifications We are looking for someone with relevant university education. You succeed with us if you meet people with respect, attentiveness, and professionalism. You feel secure in your public administration role and have the ability to build trusting relationships with people in different life situations. You are driven to develop in your professional role and want to contribute to high quality in our activities. With a structured and legally sound approach, you manage your cases while having the ability to see the bigger picture. Analytical sharpness, good judgment, and confidence in decision-making are qualities that will serve you well in this role. It is an advantage if you are a social worker with experience in public administration according to LSS and SoL. You also need to have a strong ability to express yourself clearly and professionally in speech and writing. About the Division The Disability Services Division currently consists of eleven case officers, two placement coordinators, two housing adaptation case officers, group leaders, a development manager, and a manager. Together we work to create conditions for participation, independence, and good living conditions for Sollentuna's residents. The Care and Social Services Office consists of approximately 70 employees working in areas including social services, LSS case management, finance, administration, and support and development. We actively work with quality, development, and choice to offer residents the best possible service. Other Information This is a permanent position. Selection and interviews may take place on an ongoing basis, so don't delay submitting your application. A background check will be conducted before an offer of employment is made. What We Offer We know that a sustainable working life requires the right conditions. With us, you get: A solid introduction with a designated mentor Close support from your manager, group leader, and experienced colleagues Regular case reviews, supervision, and legal support Good opportunities for professional development A welcoming team that supports each other Flexible working hours, wellness benefits, and the possibility of flexible vacation arrangements We look forward to receiving your application! Welcome to Sollentuna – a municipality in the heart of opportunities! Together we make Sollentuna better every day for our residents, entrepreneurs, and organizations. We have clear and ambitious goals to create security, welfare, and sustainable growth. We offer you a meaningful and enjoyable job in a stable environment where ambition is high. With us, you get fantastic colleagues who want to make a difference for others. Now we're looking for someone who is innovative, responsible, and welcoming. Join us on the journey to create Sweden's most attractive municipality!
Car Mechanic
Hey, we're looking for a car mechanic immediately, preferably with long experience—that's a plus, but not required. You must be able to handle tire changes/tire balancing and mechanical work.
Pharmacist with Extemporaneous Preparation Authorization — Cross-Functional Role
About AtrimusRx AtrimusRx AB is a Swedish pharmaceutical company licensed for wholesale distribution, community pharmacy, extemporaneous preparation, and handling of controlled substances. We work with licensed medicines and addressing medicine shortages, as well as developing and extemporaneously manufacturing customized, 3D-printed medications. Operations are conducted in collaboration with pharmacies, prescribers, healthcare providers, international suppliers, and manufacturers. AtrimusRx is located in Sollentuna and works with pharmaceutical supply in situations where availability, pharmaceutical quality, and time-critical decisions are critical. About the Position We are seeking a licensed pharmacist with extemporaneous preparation authorization for a cross-functional role within: Licensed medicines and medicine shortages Requisition handling in our community pharmacy Extemporaneous manufacturing of customized and 3D-printed medications You will work across multiple operational areas and switch between tasks based on current needs. This role is ideal for someone who thrives on variety and wants to apply your pharmaceutical expertise more broadly than in a traditional pharmacy setting. Work proceeds periodically at a high pace and involves multiple parallel processes. You must be able to prioritize, make well-founded decisions, and simultaneously maintain high pharmaceutical quality. We are looking for someone who wants to develop long-term with the business and is motivated by taking responsibility and delivering results. You are also expected to identify improvement opportunities, take initiative, and contribute to business development. Duties and Responsibilities Licensed Medicines and Medicine Shortages Handling inquiries and orders for licensed medicines Procurement and import of licensed medicines Contact with pharmacies, prescribers, healthcare providers, and foreign suppliers Assessment of availability, lead times, and alternative solutions Management of documentation and questions regarding quality and delivery Identification and procurement of medicines during supply shortages and crisis situations Community Pharmacy and Requisitions Handling, pharmaceutical review, and dispensing of requisitions Contact with healthcare providers and other authorized customers Verification of orders, documentation, and delivery records Ensuring that handling complies with applicable regulations and procedures Extemporaneous and 3D-Printed Medications Extemporaneous manufacturing of customized and 3D-printed medications Preparation, manufacturing, process controls, and documentation Pharmaceutical assessments and quality assurance Handling and verification of raw materials, packaging materials, and manufacturing records Participation in development of new formulations, strengths, and manufacturing processes Ensuring that manufacturing complies with applicable requirements and procedures Other pharmaceutical and administrative tasks may occur. Employment Terms Full-time employment, 40 hours per week. Fixed working hours 08:00–17:00. The position is based at AtrimusRx in Sollentuna. Remote work is not an option as the role involves work in our pharmacy and manufacturing operations. The salary range is 38,000–45,000 kronor per month. Salary within the range is determined based on relevant experience and qualifications. Apply only if the salary range meets your expectations. An extract from the criminal record will be requested. Qualifications For this position, you must: Be a licensed registered pharmacist or pharmacist Have extemporaneous preparation authorization Have at least one year of relevant work experience from a pharmacy, extemporaneous operations, or the pharmaceutical industry Be fluent in Swedish and English, both spoken and written Be able to work on-site in Sollentuna during the specified working hours It is particularly meritorious if you have: Practical experience with extemporaneous manufacturing Experience as a responsible pharmacist (Läkemedelsansvarig Apotekare, LMA) Experience with requisition handling Experience with licensed medicines and medicine shortages Personal Qualities You are thorough, responsible, and well-organized. You can prioritize multiple parallel tasks without compromising on quality or patient safety. You work independently, collaborate well, and are flexible to business needs. You are solution-oriented, take your own initiative, and follow up on what you have started. We value a professional and long-term approach. To thrive with us, you need to want to get to know the business, build specialist expertise, and actively contribute to company development. What We Offer A varied role where you combine pharmacy work with licensed medicines, addressing medicine shortages, and extemporaneous manufacturing. You will become part of a small, cross-functional team with short decision-making paths and have the opportunity to work with 3D-printed, customized medications. Application Process The recruitment process begins with two tests: A personality test that takes approximately 25 minutes. A cognitive test that takes approximately 12 minutes. The second test will be sent 24 hours after you complete the first test. Once both tests are completed, send your CV to [email protected]. All steps must be completed in the specified order. Applications that do not follow this procedure will not be considered. Thoroughness, attention to detail, and the ability to follow instructions are critical qualities for this position. The application process therefore forms part of our initial screening. Selection and interviews take place on an ongoing basis. The position may be filled before the final application deadline. We ask that you do not contact media sales representatives, recruitment consultants, or similar.
Pharmacist with Extemporaneous Preparation Authorization – Cross-Functional Role
About AtrimusRx AtrimusRx AB is a Swedish pharmaceutical company licensed for wholesale distribution, community pharmacy, extemporaneous drug preparation, and handling of controlled substances. We work with licensed medicines and address drug shortages, as well as develop and extemporaneously manufacture individualized, 3D-printed medications. Operations are conducted in collaboration with pharmacies, prescribers, healthcare providers, international suppliers, and manufacturers. AtrimusRx is based in Sollentuna and works to ensure drug supply in situations where availability, pharmaceutical quality, and time-critical decisions are critical. About the Position We are seeking a licensed pharmacist with extemporaneous preparation authorization for a cross-functional role in: Licensed medicines and drug shortage management Requisition handling within our community pharmacy Extemporaneous manufacturing of individualized and 3D-printed medications You will work across multiple operational areas and switch between tasks based on current needs. This role suits you if you thrive with variety and want to apply your pharmaceutical expertise more broadly than in a traditional pharmacy role. Work is conducted periodically at a fast pace and involves several parallel processes. You need to be able to prioritize, make well-reasoned decisions, and maintain high pharmaceutical quality simultaneously. We are looking for someone who wants to develop long-term with the organization and is motivated by taking responsibility and delivering results. You are also expected to identify improvement opportunities, take initiative, and contribute to the company's development. Responsibilities and Tasks Licensed Medicines and Drug Shortage Management Handling inquiries and orders for licensed medicines Procurement and import of licensed medicines Contact with pharmacies, prescribers, healthcare providers, and foreign suppliers Assessment of availability, lead times, and alternative solutions Management of documentation and questions regarding quality and delivery Identification and procurement of medicines during supply shortages and crisis situations Community Pharmacy and Requisitions Handling, pharmaceutical review, and dispensing of requisitions Contact with healthcare providers and other authorized purchasers Verification of orders, documentation, and delivery records Ensuring that handling complies with applicable regulations and procedures Extemporaneous and 3D-Printed Medications Extemporaneous manufacturing of individualized and 3D-printed medications Preparation, manufacturing, process controls, and documentation Pharmaceutical assessments and quality assurance Handling and control of raw materials, packaging materials, and manufacturing documentation Participation in development of new formulations, strengths, and manufacturing processes Ensuring that manufacturing complies with applicable requirements and procedures Other pharmaceutical and administrative tasks may occur. Employment Terms Full-time employment, 40 hours per week. Fixed working hours 08:00–17:00. The position is located at AtrimusRx in Sollentuna. Remote work is not an option as the role involves work in our pharmacy and manufacturing operations. Salary range: 38,000–45,000 kronor per month. Salary within the range will be determined based on relevant experience and qualifications. Please apply only if the salary range matches your expectations. A criminal background check will be requested. Qualifications For this position, you must: Be a licensed pharmacist Have extemporaneous preparation authorization Have at least one year of relevant work experience from a pharmacy, extemporaneous preparation facility, or pharmaceutical industry Be fluent in Swedish and English, both spoken and written Be able to work on-site in Sollentuna during the specified working hours It is particularly meritorious if you have: Practical experience in extemporaneous preparation Experience as a responsible pharmacist (LMA) Experience with requisition handling Experience with licensed medicines and drug shortage management Personal Qualities You are thorough, responsible, and well-organized. You can prioritize multiple parallel tasks without compromising quality or patient safety. You work independently, collaborate well, and are flexible to the organization's needs. You are solution-oriented, take initiative, and follow through on what you start. We value a professional and long-term approach. To thrive with us, you need to want to get to know the operations, build specialized expertise, and actively contribute to the company's development. What We Offer A varied role where you combine pharmacy work with licensed medicines, drug shortage management, and extemporaneous preparation. You will be part of a small, cross-functional team with short decision-making processes and have the opportunity to work with 3D-printed, individualized medications. Application Process The recruitment process begins with two tests: A personality test that takes approximately 2 minutes. A cognitive test that takes approximately 12 minutes. The second test is sent 24 hours after the first test is completed. Once both tests are completed, send your CV to [email protected]. All steps must be completed in the specified order. Applications that do not follow this process will not be considered. Accuracy, attention to detail, and ability to follow instructions are critical qualities for this position. The application process therefore forms part of our initial selection. Selection and interviews are conducted on an ongoing basis. The position may be filled before the final application deadline. We ask that you do not contact media sales representatives, recruitment consultants, or similar third parties.
GMP-Responsible Pharmacist – Extemporaneous Preparation & 3D Printing
AtrimusRx is seeking an experienced pharmacist with strong expertise in GMP and extemporaneous manufacturing who is ready to take GMP responsibility for our 3D printing operations focused on individually tailored medications. This is a central role for someone with a solid pharmaceutical and quality foundation, who is also driven by development and the opportunity to make a tangible difference for patients. We're looking for someone who is curious, enjoys solving complex problems, and gets energized – maybe even a little excited – when facing a new challenge. At AtrimusRx, pharmaceutical quality, technology, and development come together – with the patient's needs as our starting point. Why do we work with 3D printing of medications? Not all patients fit into the doses and formulations that are commercially available. This is especially true for children, where medication needs and dosing can look very different than for adults. In practice, this can mean that tablets need to be divided or crushed, or that capsule contents need to be mixed with food or drink for a child to receive their prescribed treatment. We believe there should be better options. With 3D printing of individually tailored medications, we work to be able to manufacture medications in a dose, strength, and formulation adapted to each individual patient's needs from the start. The goal is to reduce the need to manipulate medications after the fact that were not originally designed for the patient. For us, 3D printing is therefore not about the technology itself. The technology is a tool to solve a real problem for patients, families, and healthcare providers. This is the operation you will help quality assure and develop. About the role As GMP-responsible pharmacist, you will have a central function in our extemporaneous operations. You will work closely with our operational manufacturing and our pharmacists and are responsible for developing and maintaining robust quality work as the operations grow and evolve. Your work tasks include: responsibility for and further development of GMP work within the operation ensuring that processes, manufacturing, and documentation meet applicable quality and regulatory requirements responsibility for deviation management, CAPA, change control, and risk assessments driving and following up on qualification and validation of equipment, processes, and manufacturing methods developing, reviewing, and implementing SOPs, instructions, and other governing documentation ensuring structured and continuous quality work contributing quality expertise in the development and implementation of new substances, formulations, and manufacturing processes assisting with regulatory inspections and regulatory quality matters continuously identifying and driving improvements in processes, work methods, and quality systems We are looking for someone who is a licensed pharmacist or pharmaceutical technician and has: documented previous experience with GMP responsibility solid practical experience working according to GMP experience with extemporaneous manufacturing good experience with pharmaceutical quality systems and GMP documentation experience with deviation management, CAPA, change control, and risk management experience with qualification and validation good ability to interpret regulatory requirements and translate them into practical and well-functioning processes Previous experience with 3D printing is not a requirement. What matters is that you have the right pharmaceutical and GMP expertise, as well as the curiosity and willingness to learn and develop in a new area. As a person You are curious, solution-oriented, and have a genuine interest in development. You enjoy deepening your knowledge and understanding complex issues. When you encounter a problem, your natural approach is to explore the possibilities, analyze alternatives, and find a well-grounded path forward. We value people who dare to ask questions, think in new ways, and challenge established methods when there are factual reasons to do so. At the same time, you have the thoroughness, integrity, and respect for quality and regulations that are required to bear GMP responsibility. For us, curiosity and the desire to continue learning are important qualities. We believe you will thrive best with us if new challenges spark engagement rather than hesitation, and if you appreciate solving complex problems together with others. And perhaps most importantly: you understand that quality systems, processes, and documentation ultimately exist for a reason – for the patient. About AtrimusRx AtrimusRx works with complex aspects of pharmaceutical supply, including drug shortages, licensed medicines, pharmaceutical distribution, and extemporaneous manufacturing. AtrimusRx is Sweden's first open-care pharmacy that extemporaneously manufactures medications from the beginning, from APIs. Within our extemporaneous operations, we work with 3D printing of individually tailored medications to enable doses, strengths, and formulations adapted to the patient's needs. This is particularly significant for children, where available medications are not always adapted to their needs and tablets therefore may need to be divided or crushed or capsule contents mixed with food. Our ambition is for the medication to be manufactured from the start based on the patient's prescribed dose and needs. We are a specialist-driven and entrepreneurial organization where innovation and quality go hand in hand, with patient safety as the obvious starting point. As GMP-responsible pharmacist, you will become an important part of the work to develop individually tailored pharmaceutical manufacturing that can make a real difference for patients. Terms of Employment Full-time employment, 40 hours per week. Fixed hours 08:00–17:00. The position is located at AtrimusRx in Sollentuna. Remote work is not applicable as the role involves on-site work in our pharmacy and manufacturing operations. Application Process The recruitment process begins with two tests: Personality test – takes approximately 2 minutes. Cognitive test – takes approximately 12 minutes and is sent 24 hours after the first test is completed. Once both tests are completed, send your CV to [email protected]. All steps must be completed in the specified order. Applications that do not follow this procedure will not be considered. Meticulousness, attention to detail, and the ability to follow instructions are critical qualities for this position. The application process therefore forms part of our initial screening. Selection and interviews take place on an ongoing basis and the position may be filled before the final application deadline. We decline contact from media sales representatives, recruitment consultants, and other providers of recruitment and advertising services.
Traveling Service Engineer/Electrical Engineer wanted for JEOL!
We are now looking for a service engineer/electrical engineer for our client JEOL! Are you a trained engineer in electrical engineering, technical physics, or similar and looking for an exciting position in a global company? Apply today! JEOL is a global company and one of the world's leading manufacturers of electron-optical and analytical instruments as well as equipment for sample preparation. They have their headquarters in Japan and offices in over 30 countries with a total of over 3,500 employees. As a global company, they are at the forefront of development, manufacturing, and application of high-end scientific instruments. JEOL is expanding its operations and is now looking for a traveling Service Engineer for the technical support segment of electron microscopy, based in Sollentuna, Stockholm. You will be part of a small team of engineers and be responsible for installation, preventive maintenance, repairs, and troubleshooting of electron microscopes in the Nordic region. Customers include research institutes in wood, metal, and pharmaceuticals as well as universities and colleges. The work involves travel throughout the Nordic region with many overnight stays. In the longer term, there may also be trips to JEOL's development and production units in Europe and Japan. WHAT WE ARE LOOKING FOR To be considered for this position, you have a technical education at bachelor's level or higher, for example in electrical engineering, technical physics, or similar. If you have completed a vocational higher education in a relevant field, that is also relevant. You have good knowledge of Swedish and English and preferably a Nordic language. The position requires a B-class driver's license and we prefer that you have access to a car. As a person, you are a quick learner, very technically interested, and passionate about technical problem-solving. Initially, you will travel with experienced colleagues, but over time you will work independently with JEOL's various customers. You therefore enjoy working independently but have no problem meeting different types of people, are service-oriented, and flexible. It is highly meritorious if you have previously worked with support of technical equipment, such as various analytical instruments. It is also advantageous if you have the ability to perform systematic troubleshooting in a complex system, including electronics, computers, vacuum technology, and mechanics. This position is a direct recruitment, which means you will be employed by JEOL and will start with a 6-month probationary period. We at StudentConsulting are responsible for the recruitment process, and if you have any questions about the role, feel free to contact the responsible recruiter. You will be based at their office in Sollentuna. This is a full-time position and working hours are 8:30-17:00. Is this you we are describing? Apply today! Selection and interviews are held on a rolling basis and the position will be filled when we find the right candidate.
QA Specialist – GMP & Extemporaneous
Do you want to work with quality in an operation where pharmaceutical manufacturing, innovation, and regulatory requirements meet? AtrimusRx is seeking a QA Specialist for our growing extemporaneous pharmacy operation in Sollentuna. With us, you'll work close to the operations and help develop quality processes within personalized pharmaceutical manufacturing, extemporaneous preparation, and new manufacturing techniques. This is a role for someone with QA and GMP experience who wants to work in an environment where quality isn't just about managing existing processes, but also about developing them. About the role As a QA Specialist, you'll be a central part of our quality work and will collaborate closely with pharmacists, production, development, and management. Your responsibilities will include: development and maintenance of quality systems working with GMP and regulatory requirements for pharmaceutical manufacturing creating, reviewing, and updating SOPs and other quality documentation deviation management, CAPA, and change control risk assessments and Quality Risk Management qualification and validation of equipment, processes, and methods review of manufacturing and quality documentation supplier assessments and quality agreements training staff on GMP and quality internal audits and quality monitoring preparations for and participation in regulatory inspections development and improvement of processes within our extemporaneous operation Depending on your experience and qualifications, the role can also develop into greater quality responsibility within the operation. Who are we looking for? We're seeking someone with relevant QA and GMP experience in pharmaceutical manufacturing. You may currently work as, for example: QA Specialist Senior QA Specialist QA Manager Validation Specialist Quality Manager Production Pharmacist Pharmacist in extemporaneous manufacturing or in a corresponding quality function in the pharmaceutical industry We'd particularly like to see experience in one or more of the following areas: pharmaceutical manufacturing extemporaneous manufacturing pharmaceutical industry hospital pharmacy with manufacturing validation and qualification deviation management and CAPA change control Quality Risk Management regulatory inspections working with quality systems in regulated operations Pharmaceutical education is a merit, especially if you're a pharmacist or pharmacy technician with experience in pharmaceutical manufacturing or extemporaneous preparation. For candidates with the right education and experience, there may also be an opportunity to take on formal GMP responsibility within the operation over time. About you We believe you are structured, thorough, and quality-conscious, but also pragmatic and solution-oriented. You need to understand both regulatory requirements and the practical operations behind them. We especially appreciate people who: view quality as a support for operations, not as an administrative function on the side are willing to identify problems and drive improvements can work independently and take responsibility thrive with short decision-making paths enjoy building structures and processes have high integrity and a strong quality mindset are curious about new working methods and techniques Why AtrimusRx? AtrimusRx works with pharmaceutical supply, drug shortages, licensed medicines, and extemporaneous manufacturing. Within our extemporaneous operation, we work with personalized pharmaceutical manufacturing and develop new opportunities to manufacture medicines in strengths and formulations adapted to the patient's needs. We work with, among other things, 3D printing of medicines, which means that quality and regulatory issues are an integrated part of both development and manufacturing. With us, you'll therefore have the opportunity to work in an operation where QA is closely linked to development, production, and innovation. You'll be part of a smaller, entrepreneurial company with short decision-making paths and great ambitions. Practical information Location: Sollentuna Scope: Full-time Start date: As agreed Application process The recruitment process begins with two tests: A personality test that takes approximately 2 minutes. A cognitive test that takes approximately 12 minutes. The second test will be sent 24 hours after the first test is completed. Once both tests are completed, send your CV to [email protected]. All steps must be completed in the specified order. Applications that do not follow this procedure will not be considered. Accuracy, attention to detail, and the ability to follow instructions are crucial qualities for this position. The application process therefore forms part of our initial selection. Selection and interviews take place on an ongoing basis. The position may be filled before the final application deadline. We ask that you do not contact media sales representatives, recruitment consultants, or similar.
Pharmacist with Extemporaneous Compounding Authorization – Cross-Functional Role
About AtrimusRx AtrimusRx AB is a Swedish pharmaceutical company licensed for wholesale distribution, community pharmacy operations, extemporaneous compounding, and handling of controlled substances. We work with licensed medicines and medicine shortages, as well as with the development and extemporaneous compounding of individualized, 3D-printed medications. Operations are conducted in collaboration with pharmacies, prescribers, healthcare providers, international suppliers, and manufacturers. AtrimusRx is located in Sollentuna and works with pharmaceutical supply in situations where availability, pharmaceutical quality, and time-critical decisions are decisive. About the Position We are looking for a licensed pharmacist with extemporaneous compounding authorization for a cross-functional role within: Licensed medicines and medicine shortages Requisition handling in our community pharmacy Extemporaneous compounding of individualized and 3D-printed medications You will work across multiple operational areas and switch between tasks based on current needs. This role is ideal for someone who thrives with variety and wants to apply your pharmaceutical expertise more broadly than in a traditional pharmacy role. Work is conducted periodically at a high pace and involves multiple parallel processes. You need to be able to prioritize, make well-founded decisions, and simultaneously maintain high pharmaceutical quality. We are looking for someone who wants to develop long-term with the business and is motivated by taking responsibility and delivering results. You are also expected to identify improvement opportunities, take initiative, and contribute to the company's development. Duties and Responsibilities Licensed Medicines and Medicine Shortages Handling requests and orders for licensed medicines Procurement and import of licensed medicines Contact with pharmacies, prescribers, healthcare providers, and foreign suppliers Assessment of availability, lead times, and alternative solutions Handling of documentation and issues related to quality and delivery Identification and procurement of medicines in shortage situations Community Pharmacy and Requisitions Handling, pharmaceutical verification, and dispensing of requisitions Contact with healthcare providers and other authorized purchasers Verification of orders, documentation, and delivery records Ensuring that handling complies with applicable regulations and procedures Extemporaneous and 3D-Printed Medications Extemporaneous compounding of individualized and 3D-printed medications Preparation, manufacturing, process controls, and documentation Pharmaceutical assessments and quality assurance Handling and verification of raw materials, packaging materials, and manufacturing documentation Participation in development of new formulations, strengths, and manufacturing processes Ensuring that manufacturing complies with applicable requirements and procedures Other pharmaceutical and administrative tasks may occur. Terms of Employment Full-time position, 40 hours per week. Fixed working hours 08.00–17.00. The position is located at AtrimusRx in Sollentuna. Remote work is not an option as the role includes work in our pharmacy and manufacturing operations. Salary range is 38,000–45,000 kronor per month. Salary within the range is determined based on relevant experience and qualifications. Apply only if the salary range meets your expectations. A criminal record extract will be requested. Qualifications For this position, you must: Be a licensed pharmacist or registered pharmacy technician Have extemporaneous compounding authorization Have at least one year of relevant work experience from a pharmacy, compounding facility, or pharmaceutical industry Speak and write Swedish and English fluently Be able to work on-site in Sollentuna during the specified working hours It is particularly meritorious if you have: Practical experience in extemporaneous compounding Experience as a responsible pharmacist (LMA) Experience with requisition handling Experience with licensed medicines and medicine shortages Personal Qualities You are thorough, responsible, and organized. You can prioritize multiple parallel tasks without compromising on quality or patient safety. You work independently, collaborate well, and are flexible to the company's needs. You are solution-oriented, take your own initiative, and follow up on what you have started. We value a professional and long-term approach. To thrive with us, you need to be willing to get to know the business, build specialized expertise, and actively contribute to the company's development. What We Offer A varied role where you combine pharmacy work with licensed medicines, medicine shortages, and extemporaneous compounding. You will be part of a small, cross-functional team with short decision-making paths and get the opportunity to work with 3D-printed, individualized medications. Application Process The recruitment process begins with two tests: A personality test taking approximately 2 minutes. A cognitive test taking approximately 12 minutes. The second test is sent 24 hours after the first test is completed. Once both tests are completed, send your CV to [email protected]. All steps must be completed in the specified order. Applications not following this procedure will not be considered. Accuracy, attention to detail, and the ability to follow instructions are critical qualities for this position. The application process therefore forms part of our initial screening. Selection and interviews take place on an ongoing basis. The position may be filled before the final application deadline. We do not accept contact from media salespeople, recruitment consultants, or similar.
QA Specialist – GMP & Extemporaneous
Do you want to work with quality in an operation where pharmaceutical manufacturing, innovation, and regulatory requirements meet? AtrimusRx is looking for a QA Specialist for our growing extemporaneous pharmacy operation in Sollentuna. With us, you'll work close to the operation and help develop quality processes within personalized pharmaceutical manufacturing, extemporaneous preparation, and new manufacturing techniques. This is a role for someone with QA and GMP experience who wants to work in an environment where quality is not just about maintaining existing processes, but also about developing them. About the Role As a QA Specialist, you'll be a central part of our quality work and collaborate closely with pharmacists, production, development, and management. Your responsibilities will include: developing and maintaining quality systems working with GMP and regulatory requirements for pharmaceutical manufacturing creating, reviewing, and updating SOPs and other quality documentation deviation management, CAPA, and change control risk assessments and Quality Risk Management qualification and validation of equipment, processes, and methods review of manufacturing and quality documentation supplier assessments and quality agreements training personnel on GMP and quality internal inspections and quality monitoring preparations for and participation in regulatory inspections developing and improving processes within our extemporaneous operation Depending on your experience and expertise, the role can develop into greater quality responsibility within the operation. Who Are We Looking For? We are looking for someone with relevant QA and GMP experience in pharmaceutical manufacturing. You might currently work as: QA Specialist Senior QA Specialist QA Manager Validation Specialist Quality Responsible Production Pharmacist Pharmacist in extemporaneous manufacturing or in a similar quality function within the pharmaceutical industry We would appreciate if you have experience from one or more of the following areas: pharmaceutical manufacturing extemporaneous manufacturing pharmaceutical industry hospital pharmacy with manufacturing validation and qualification deviation management and CAPA change control Quality Risk Management regulatory inspections working with quality systems in regulated operations Pharmaceutical education is a merit, especially if you are a pharmacist or pharmacy technician with experience in pharmaceutical manufacturing or extemporaneous preparation. For candidates with the right education and experience, there may also be an opportunity in the long term to assume formal GMP responsibility within the operation. About You We believe you are structured, thorough, and quality-conscious, yet pragmatic and solution-oriented. You need to be able to understand both regulatory requirements and the practical operations behind them. We especially appreciate people who: view quality as a support for the operation, not as an administrative function on the side are willing to identify problems and drive improvements can work independently and take responsibility enjoy short decision-making paths like building structures and processes have high integrity and a strong quality mindset are curious about new ways of working and techniques Why AtrimusRx? AtrimusRx works with pharmaceutical supply, drug shortages, licensed medicines, and extemporaneous manufacturing. Within our extemporaneous operation, we work with personalized pharmaceutical manufacturing and develop new ways to manufacture medicines in strengths and formulations adapted to the patient's needs. We work with, among other things, 3D printing of medicines, which means that quality and regulatory matters are an integrated part of both development and manufacturing. With us, you'll therefore have the opportunity to work in an operation where QA is closely linked to development, production, and innovation. You'll be part of a small and entrepreneurial company with short decision-making paths and big ambitions. Practical Information Location: Sollentuna Scope: Full-time Start Date: By agreement Application Process The recruitment process begins with two tests: A personality test that takes approximately 2 minutes. A cognitive test that takes approximately 12 minutes. The second test is sent 24 hours after the first test is completed. Once both tests are completed, send your CV to [email protected]. All steps must be completed in the specified order. Applications that do not follow this procedure will not be considered. Thoroughness, attention to detail, and the ability to follow instructions are critical qualities for this position. The application process therefore forms part of our initial screening. Selection and interviews are ongoing. The position may be filled before the final application deadline. We do not accept contact from media sales, recruitment consultants, and similar.
QA Specialist – GMP & Extemporaneous Pharmacy
Do you want to work with quality in an operation where pharmaceutical manufacturing, innovation, and regulatory requirements converge? AtrimusRx is seeking a QA Specialist for our growing extemporaneous pharmacy operations in Sollentuna. With us, you'll work closely with operations and help develop quality processes in personalized pharmaceutical manufacturing, extemporaneous pharmacy, and new manufacturing techniques. This is a role for someone with QA and GMP experience who wants to work in an environment where quality is not just about maintaining existing processes, but also about developing them. About the Role As a QA Specialist, you'll be a central part of our quality efforts and work closely with pharmacists, production, development, and management. Your responsibilities will include: development and management of quality systems working with GMP and regulatory requirements for pharmaceutical manufacturing preparing, reviewing, and updating SOPs and other quality documentation deviation handling, CAPA, and change control risk assessments and Quality Risk Management qualification and validation of equipment, processes, and methods review of manufacturing and quality documentation supplier assessments and quality agreements training personnel on GMP and quality internal inspections and quality monitoring preparations for and participation in regulatory inspections development and improvement of processes within our extemporaneous pharmacy operations Depending on your experience and competency, the role may develop into greater quality responsibility within the operation. Who We're Looking For We're seeking someone with relevant QA and GMP experience in pharmaceutical manufacturing. You may currently work as, for example: QA Specialist Senior QA Specialist QA Manager Validation Specialist Quality Manager Production Pharmacist Pharmacist in Extemporaneous Pharmacy or in an equivalent quality function within the pharmaceutical industry We'd like to see experience from one or more of the following areas: pharmaceutical manufacturing extemporaneous pharmacy manufacturing pharmaceutical industry hospital pharmacy with manufacturing validation and qualification deviation handling and CAPA change control Quality Risk Management regulatory inspections working with quality systems in regulated operations Pharmaceutical education is a merit, especially if you're a pharmacist or pharmacy technician with manufacturing or extemporaneous pharmacy experience. For candidates with the right education and experience, there may also be an opportunity over time to take on formal GMP responsibility within the operation. About You We believe you're structured, thorough, and quality-conscious, yet pragmatic and solution-oriented. You need to understand both regulatory requirements and the practical operations behind them. We especially appreciate people who: view quality as a support for operations, not as an administrative function separate from the business are willing to identify problems and drive improvements can work independently and take responsibility enjoy short decision-making processes like building structures and processes have high integrity and a strong quality mindset are curious about new work methods and techniques Why AtrimusRx? AtrimusRx works with pharmaceutical supply, drug shortages, licensed medicines, and extemporaneous pharmacy manufacturing. Within our extemporaneous pharmacy operations, we work with personalized pharmaceutical manufacturing and develop new opportunities to produce medicines in strengths and formulations tailored to patient needs. We work with 3D-printing of pharmaceuticals, among other things, which means that quality and regulatory matters are an integrated part of both development and manufacturing. With us, you'll have the opportunity to work in an operation where QA is closely linked to development, production, and innovation. You'll become part of a smaller, entrepreneurial company with short decision-making processes and great ambitions. Practical Information Location: Sollentuna Full-time Start Date: By agreement Application Process The recruitment process begins with two tests: A personality test taking approximately 2 minutes. A cognitive test taking approximately 12 minutes. The second test is sent 24 hours after the first test is completed. Once both tests are completed, send your CV to [email protected]. All steps must be completed in the specified order. Applications that do not follow this procedure will not be considered. Thoroughness, attention to detail, and ability to follow instructions are critical qualities for this position. The application process therefore forms part of our initial screening. Selection and interviews are ongoing. The position may be filled before the final application deadline. We request that media sales representatives, recruitment consultants, and similar professionals do not contact us.
QA Specialist – GMP & Extemporaneous
Do you want to work with quality in an operation where pharmaceutical manufacturing, innovation, and regulatory requirements converge? AtrimusRx is seeking a QA Specialist for our growing extemporaneous pharmacy operation in Sollentuna. With us, you'll work closely with operations and help develop quality practices in personalized pharmaceutical manufacturing, extemporaneous compounding, and new manufacturing techniques. This is a role for someone with QA and GMP experience who wants to work in an environment where quality isn't just about maintaining existing processes, but also about developing them. About the Role As a QA Specialist, you'll be a key part of our quality efforts and work closely with pharmacists, production, development, and management. Your responsibilities will include: development and maintenance of quality systems working with GMP and regulatory requirements for pharmaceutical manufacturing creating, reviewing, and updating SOPs and other quality documentation deviation handling, CAPA, and change control risk assessments and Quality Risk Management qualification and validation of equipment, processes, and methods review of manufacturing and quality documentation vendor assessments and quality agreements training staff in GMP and quality internal inspections and quality monitoring preparations for and participation in regulatory inspections development and improvement of processes in our extemporaneous operations Depending on your experience and expertise, the role can also develop into greater quality responsibility within the operation. Who Are We Looking For? We're seeking someone with relevant QA and GMP experience in pharmaceutical manufacturing. You may currently work as, for example: QA Specialist Senior QA Specialist QA Manager Validation Specialist Quality Manager Production Pharmacist Pharmacist in extemporaneous compounding or in a corresponding quality function in the pharmaceutical industry We would be pleased if you have experience from one or more of the following areas: pharmaceutical manufacturing extemporaneous compounding pharmaceutical industry hospital pharmacy with manufacturing validation and qualification deviation handling and CAPA change control Quality Risk Management regulatory inspections working with quality systems in regulated operations Pharmaceutical education is a merit, especially if you are a pharmacist or pharmacy technician with experience in pharmaceutical manufacturing or extemporaneous compounding. For candidates with the right education and experience, there may be an opportunity to take on formal GMP responsibility within the operation in the future. As a Person We believe you are structured, thorough, and quality-minded, but also pragmatic and solution-oriented. You need to understand both regulatory requirements and the practical operations behind them. We especially appreciate people who: see quality as a support for operations, not as an administrative function separate from the business dare to identify problems and drive improvements can work independently and take responsibility thrive with short decision-making paths enjoy building structures and processes have high integrity and a strong quality mindset are curious about new working methods and techniques Why AtrimusRx? AtrimusRx works with pharmaceutical supply, medicine shortages, licensed medicines, and extemporaneous compounding. Within our extemporaneous operations, we work with personalized pharmaceutical manufacturing and develop new ways to produce medicines in strengths and formulations tailored to patient needs. We work with, among other things, 3D printing of pharmaceuticals, which means quality and regulatory matters are an integrated part of both development and manufacturing. With us, you'll have the opportunity to work in an operation where QA is closely linked to development, production, and innovation. You'll be part of a smaller, entrepreneurial company with short decision-making paths and great ambitions. Practical Information Location: Sollentuna Full-time Start: By agreement Application Process The recruitment process begins with two tests: A personality test that takes approximately 2 minutes. A cognitive test that takes approximately 12 minutes. The second test is sent 24 hours after the first test is completed. Once both tests are completed, send your CV to [email protected]. All steps must be completed in the specified order. Applications that do not follow this procedure will not be considered. Thoroughness, attention to detail, and the ability to follow instructions are critical qualities for this position. The application process is therefore part of our initial screening. Selection and interviews are ongoing. The position may be filled before the final application deadline. We do not welcome contact from media sales representatives, recruitment consultants, and similar.