Senior Global Project Manager

Ramboll Sweden AB

Om rollen Are you passionate about health and safety? Do you believe safety starts with quality? Do you enjoy making tools and processes work well together and get motivated by helping others succeed? If this sounds like you, or you’re curious to learn more, then this role could be the perfect opportunity. Join our business area, Buildings, in Sweden as our new HSEQ Lead and work with us to close the gap to a sustainable future! Your new role As our HSEQ Lead, you will play a key role in strengthening Ramboll’s safety culture and quality focus in Sweden. You will lead the local implementation of the global HSEQ Buildings strategy and will act as a sparring partner to senior managers in Sweden on all aspects of HSEQ management. In addition, you will collaborate with peers across other geographies and contribute to the Global Buildings HSEQ network, sharing best practices and supporting ongoing development. In this role, you will also play an active role in supporting project delivery teams, acting as a trusted HSEQ advisor and contributing with your specialist knowledge to the successful delivery of key client projects. Your key responsibilities will be: Ensuring implementation of Ramboll’s HSEQ management system, in compliance with local regulations. Audit management and non-conformities handling to ensure safety and quality of project delivery. Follow up project-related work observation reports, and investigation of project-related near misses and incidents. Evaluating, analysing and reporting on HSEQ KPIs. Actively contribute to continuous improvements of Ramboll’s systems. Provide HSEQ support in client projects, including serving as the dedicated HSEQ Lead on large, strategically important projects. Location is preferably in Stockholm, Gothenburg or Malmö but Ramboll has offices in other parts of the country as well, and we are open to considering applications from those locations. At times some travel to other offices in the country may be required. About you Degree in a relevant discipline (e.g. related to the Built Environment, Health and Safety, Construction Management or similar). Experience of HSEQ in buildings and/or construction engineering projects. Experience of management systems and good understanding of local legislation. Experience of investigation and root cause analysis of near misses and incidents. Good communication skills, both writing and verbally, in Swedish and English. What we can offer you Interesting projects where you will contribute to making a real difference Commitment to your development A culture that welcomes you as the unique person you are. The long-term thinking of a foundation-owned company, with leaders guided by our Leadership Principles. Flexible working environment with the possibility of working from home up to 2 days a week. Private health insurance. Wellness benefit contribution of up to 4.000 SEK/year. Ready to join us? Please submit your application and CV online. We invite diversity in all its forms and encourage applicants from all groups to apply. We recognise that some candidates only apply when they tick every box. However, passion and potential often outweigh a perfect resume and Ramboll’s supportive learning culture can help you grow. So if this role resonates with you but you don't meet all the requirements, we encourage you to apply. You might be the perfect fit for this opportunity or another within our team. Deadline: 2026-07-31. We review applications on an ongoing basis so don’t hesitate to submit yours. Work at the heart of sustainable change with Ramboll ​Ramboll is a global architecture, engineering, and consultancy company. As a foundation-owned people company, founded in Denmark, we believe that the purpose of sustainable change is to create a thriving world for both nature and people. So, that’s where we start – and how we work. Our history is rooted in a clear vision of how a responsible company should act and being open and curious is a cornerstone of our culture. Ramboll employs more than 18,000 people globally across 35 countries. Ramboll experts deliver innovative solutions across Buildings, Transport, Water, Environment & Health, Energy, Management Consulting, and Architecture & Landscape. Combining local experience with global knowledge, we help shape the societies of tomorrow. Equality, Diversity, and Inclusion Equality, diversity, and inclusion are at the heart of what we do. At Ramboll, we believe that diversity is a strength and that different experiences and perspectives are essential to creating truly sustainable societies. We are committed to providing an inclusive and supportive work environment where everyone is able to flourish and reach their potential. At Ramboll, we offer flexibility as part of our positive and inclusive approach to work. We invite applications from candidates of all backgrounds and characteristics. Please let us know if there are any changes we could make to the application process to make it more comfortable for you. You can contact us at job.advert.accessibility@ramboll.com with such requests.

Nouryon AB

At Nouryon, our global team takes positive action every day, to reach higher collectively and individually. We create innovative and sustainable solutions for our customers to answer society’s needs – today and in the future. We are looking for team members who bring ideas forward, champion others and work together to do better. Does that sound like you? About the job As a Toxicologist you perform mainly human health hazard and risk assessments for substance registrations; study monitoring of hazard studies is part of this. In your future role as Toxicologist you will Contribute with toxicological expertise in product safety and compliance work related to substance registrations, mainly for EU REACH Commission and validate toxicity studies to be used for human hazard assessments Act as Study Monitor for guideline studies performed in GLP compliant contract research laboratories Compile scientifically based (cost-effective) testing strategies, including grouping and read across Perform human health hazard and risk assessments Advise on the toxicological profile of a substance or product to RD&I and business Communicate complex toxicological matters simply to business Take part in consortia meetings and Cefic networks and/or issue teams We believe you bring Some experience in regulatory toxicology in the chemical industry Some experience in hazard and risk assessments for regulatory purposes Knowledge of (alternative) test methods used in toxicology including higher tier testing Knowledge of regulatory requirements and their potential influence on business A business‑ and solution‑oriented mindset, with the ability to think beyond standard protocols Strong analytical and organizational skills, with the ability to work independently and act with integrity Excellent written and spoken English As a person you are flexible and enjoy working in a dynamic and changing work environment. You have excellent interpersonal, communication, and influencing skills. You also have strong networking skills, with the ability to collaborate effectively both internally and externally. At Nouryon, we provide a great job and friendly coworkers, plus benefits in addition to salary. Our collective agreement is with IKEM. Plus, we offer unilateral perks, such as bonus, reduced hours, health care allowance, lunch allowance, and more. Have we got your interest? This is a permanent position on a full-time basis, based in Gothenburg Sweden or Mumbai India. You will report to Josje Arts, Senior Toxicologist and based in Amsterdam. Please apply via our online recruitment system. We will not accept applications via e-mail. Once it's with us we will review to see if we have a match between your skills and the role! For more information about our hiring process, visit: nouryon.com/careers/how-we-hire/ As an applicant, you will be subject to a background check before employment. You will receive more information about this later in the recruitment process We work actively and systematically with HSE matters to ensure a safe and sustainable working environment for our employees. As an employee, you may therefore be required to undergo drug testing on a random basis. This is part of our commitment to safeguarding the safety and well-being of our staff We look forward to receiving your application! Contact If you have any questions about the recruitment process or your application or need assistance, please contact: Recruiting.SE@Nouryon.com #WeAreNouryon #GrowWithUs We have already chosen our sourcing channels for this recruitment and kindly ask not to be contacted by any advertisement agents, recruitment agencies or staffing companies. (#LI-Onsite)

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. Are you the right person for the assignment, or do you want to recommend a strong candidate? Do not hesitate to contact us. Apply today, selection and interviews are ongoing. Job summary We are looking for a Scientist In Vivo & In Vitro respiratory for our client. About the role: Join the Bioscience Asthma & Skin Immunity in vivo team within Research and Early Development, Respiratory & Immunology. You will support in vitro and in vivo studies, and ex vivo analyses. Respiratory & Immunology is one of AstraZeneca’s core therapy areas, aiming to understand, treat, modify, and ultimately cure respiratory and autoimmune diseases. What you will do: • Plan and execute experiments: Design, perform, and analyze in vitro and ex vivo studies to advance drug discovery projects and generate publishable insights. • Support in vivo experiments Accountabilities: • Hands on work: Conduct in vitro and ex vivo analysis from rodent studies alongside a team of committed scientists; support in vivo scientists with preparations for experiments, collecting biological samples and live animal handling. • Data responsibilities: Uphold the highest standards of data integrity, quality control, and archiving. • Communication: Evaluate and interpret primary data; write reports and summaries; present in team and project meetings. Essential for the role: • Cellular/molecular techniques: Ability to independently plan, execute, and analyze protein expression/activation assays (ELISA, Meso Scale Discovery) and RNA analysis (extraction, qRT PCR). • In vivo experience: Hands-on experience with rodents including live animal handling, drug administration through different routes, blood and organ sampling and processing. Valid education required for compliance to work with live animals in Sweden (LAS, FELASA) • Data and statistics: Understanding statistical methods, quality control, reporting, and data archiving. • M.Sc. degree in relevant subjects or equivalent level of understanding developed through experience in academia or drug discovery settings. Desirable for the role: • Experience in lung function measurements in rodents Soft skills: • Communication: Excellent written and spoken English • Strong presentation skills. Startdatum: 2026-04-20 Slutdatum: 2026-12-31 Application Deadline: 2026-03-30 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, employment, 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.