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Norvion Systems AB

CAE Crash Safety Analysis Engineer – Automotive Safety Development About Norvion Systems AB Norvion Systems AB, headquartered in Gothenburg, Sweden, is an innovative engineering company delivering advanced AI, robotics, embedded systems, and automotive engineering solutions across the Nordic region and Europe. We work closely with leading industrial partners to support the development and deployment of next-generation technologies. Our engineering teams combine deep industry experience with a practical Nordic engineering culture focused on innovation, quality, and real-world impact. To support one of our automotive partners in Gothenburg, we are looking for an experienced CAE Crash Safety Analysis Engineer to join an exciting long-term vehicle safety development assignment. If you have experience in crash simulation, occupant protection, CAE modelling, or automotive safety engineering, we would love to hear from you. About the Assignment As a CAE Crash Safety Analysis Engineer, you will contribute to the development of future vehicle safety solutions by performing advanced simulation activities and supporting engineering decisions throughout the product development lifecycle. You will work closely with multidisciplinary engineering teams to analyze vehicle crash performance, improve simulation methodologies, and support occupant protection development. Key Responsibilities Perform advanced CAE crash simulations and occupant safety analysis Develop, maintain, and improve finite element simulation models Analyze virtual simulation results and physical crash test data Support vehicle safety development through simulation-driven engineering decisions Investigate technical issues and propose improvement solutions Collaborate with design, testing, and engineering teams throughout the development process We Are Looking For We are looking for engineers with a strong background in automotive safety engineering and CAE simulation. You should have: B.Sc. or M.Sc. degree in Mechanical Engineering, Vehicle Engineering, Automotive Engineering, or a related field Professional experience in CAE crash analysis and finite element simulations Hands-on experience with crash simulation tools such as: LS-DYNA ANSA META Post Experience with occupant protection analysis and crash test dummy modelling Strong analytical and problem-solving skills Ability to work independently and collaboratively in a multidisciplinary engineering environment Fluent English communication skills Advantageous Experience The following experience will be considered a strong advantage: Human Body Models (HBM) Physical crash testing Python or MATLAB scripting Previous experience with OEM automotive safety projects Assignment Details 📍 Location: Gothenburg, Sweden (On-site) 📅 Start Date: August 2026 🏢 Assignment Type: Long-term automotive engineering assignment Candidates should already have the legal right to work in Sweden or be able to start without requiring a new work permit. Why Join Norvion? Engineering Beyond Boundaries At Norvion, engineers work on real industrial challenges involving advanced automotive technologies, AI, robotics, and intelligent systems. Work With Experienced Engineers Join a team with strong European engineering experience and collaborate with experts from leading technology companies and automotive organizations. Nordic Engineering Culture We believe in: Flat communication Technical excellence Individual ownership Continuous learning Sustainable work-life balance Interested? Please send your English CV to: 📧 hr@norviontech.com Even if this specific assignment is not the perfect match, we welcome experienced engineers to join the Norvion Talent Network.

Surely Sci & Tech AB

Job Opportunity: Senior Production Engineer (Robotics) Location: Västerås, Sweden Remote: 0% (On-site role) Role: Senior Production Engineer – Assembly We are looking for a Senior Production Engineer to support the development of assembly lines in both the current factory and the new Robotics Campus Sweden. Key Responsibilities: • Work closely with line technicians and operators in daily production activities • Conduct weekly meetings with line managers and support teams • Develop assembly methods, work instructions, and PFMEA • Ensure proper tools are available at the right stations • Drive improvements in safety, quality, and delivery performance • Support problem-solving and process optimization in production Requirements: • Minimum 5+ years’ experience as a Production Engineer in assembly manufacturing • MSc in Production Engineering, Supply Chain, or related field • Strong knowledge of ERP systems • Experience in Lean & World Class Manufacturing Personal Traits: • Strong sense of urgency and ownership • Continuous improvement mindset • High responsibility and proactive attitude Skills Needed: Production Engineering | Manufacturing | Supply Chain | ERP | Lean | WCM Why Join Surely Sci & Tech? ✔️ Permanent employment (conditions apply) ✔️ Competitive salary ✔️ Comprehensive health insurance ✔️ 5,000 SEK annual wellness benefit ✔️ VISA & work permit application support ✔️ Career development opportunities ✔️ Exciting consulting assignments with leading Nordic companies Interviews are ongoing. Apply ASAP 📩 Interested? Send your CV to Surelyscitech@outlook.com

Professional Galaxy AB

Professional Galaxy is an IT and technology consulting company that provides highly specialized expertise within IT, software development, SAP, purchasing, electronics and mechanical design. We collaborate with experienced senior experts and deliver strategic value-creating expertise to some of Sweden's most complex and analytically demanding projects. Our focus is always on high quality, professionalism and clear, measurable results. We are now seeking a Supply Chain Manager for Clinical Trial medications for one of our clients. About the assignment: Would you like to utilize your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines. We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity at the right time for every patient taking part in xx trials all over the world. Our goal is to never miss a patient. In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture. Tasks and responsibilities/The role: In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study. To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills. Your main responsibilities will include: • Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply. • Ensure effective communication with project teams and key partners across a global network. • Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies. • Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction. • Manage the Interactive Response Technology (IRT) system to execute demand and supply planning. • Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls. Soft skills: • Strong influencing, negotiating and problem-solving skills, across geographical and cultural boundaries • Ability to adapt and operate in bespoke multiple systems. Desirable for the role: • Awareness of GMP (Good Manufacturing Practise) and GCP (Good Clinical Practice) • Knowledge of clinical development processes relevant to the supply of clinical materials • Lean knowledge and understanding • Experienced in handling Quality Events (Deviations, Change Controls, Complaints Location: Göteborg Start date: 2026-06-01 End date: 2027-05-31 Application Deadline: 2026-04-19 Are you the right person for the assignment, or do you want to recommend a strong candidate? Do not hesitate to contact us. Please apply directly through our system with: - Your updated CV in english - Availability to start the assignment In the motivation, describe why you are suitable for this assignment - refer to previous consulting assignments, employmxent, education and personal qualities. Please note: We do not accept any applications through mail. All applications have to be sent through the portal to be valid. Offer continuously: Please note that for this role we offer continuously. That means that we sometimes remove the assignments before the deadline. If you are interested, we recommend that you apply immediately.