Alfa Laval Technologies AB

Every day, we get opportunities to make a positive impact - on our colleagues, partners, customers, and society. Together, we're pioneering the solutions of the future and unlocking the full potential of precious resources. Trusted to act on initiative, we challenge conventional thinking to develop world-leading technologies that inspire progress in vital areas, including energy, food, water, and shipping. As we push forward, the innovative, open spirit that fuels our 140-year-old start-up culture and rapid growth also drives our personal growth. So, as we shape a more resourceful, less wasteful world, we build our careers too. About the job You will join a global team working at the forefront of an evolving pharmaceutical technology, with significant opportunities to shape how Single-Use separation is adopted worldwide. The role gives you broad exposure to customers, production processes and sales organizations across the world, while allowing you to work alongside colleagues with deep commercial and industry expertise. With us you will have the opportunity to combine technical depth with real customer impact, playing a visible role in bringing a more flexible and efficient separation technology to the pharmaceutical industry. As a Global Business & Application Engineer - Single-Use, you will work closely with customers, sales companies and colleagues across the global organization to support the conversion from conventional filtration to Single-Use high-speed separation technology. You will act as the technical bridge between the global sales team, the local sales organizations and the customers, providing hands-on support on validation, process understanding and production scale-up while identifying new business opportunities along the way. Key responsibilities: Proactively identify and qualify new business opportunities within existing accounts, tied to production scale-up and expansion. Drive business growth by turning technical and application support into long-term customer adoption of Single-Use separation technology by performing hands-on technical work for trials & testing. Support Alfa Laval sales companies and customers directly on validation activities and general process troubleshooting related to Single-Use separators. Support the technology conversion narrative - helping customers and local teams understand the shift from conventional filtration to Single-Use separation technology. Follow market and process developments in Single Use separation to continuously strengthen internal and external knowledge. The position is based in Flemingsberg, but for the right candidate location can also be Lund, Kolding or Søborg. The role requires frequent global travelling, approximately 70 - 80 days per year. You will be part of a team of eight experienced colleagues who look forward welcoming you to the world of Alfa Laval. Who you are You are commercially driven with a strong business mindset. We believe you are a technically curious person who enjoys being close to production processes, solving real problems and turning technical understanding into customer trust and business results. You are confident in explaining complex technical value propositions in a simple, credible way, both to customers and to the internal organization. You thrive in a global, cross-functional environment and maintain your drive and patience when supporting the adoption of a technology that is still building momentum in the market. What you know To succeed, you combine a commercial mindset with a strong technical and application expertise. You have an understanding of separation technology, ideally with exposure to Single Use separator systems. Key in this role is communication and relationship-building skills, with the ability to interact with customers and internal stakeholders at different levels. Requirements: Engineering degree or equivalent technical education (biotechnology, chemical engineering, bioprocess engineering or similar). A few years of experience in sales or business development, in a complex technical sales-based environment. Familiarity with validation principles (IQ/OQ/PQ, GMP context) relevant to pharmaceutical production environments. Familiarity with filtration technologies is a merit, as it provides a valuable comparative reference point for this technology conversion story. Excellent communication skills in English in addition to either Swedish or Danish depending on your location. Merit: Knowledge of bioprocessing / up- or downstream processing in biopharma production. Driving licence Please send your application no later than November 6, 2026. We will remove the job advert from our website as soon as we have found the right candidate, so don't wait too long! At Alfa Laval, we pride ourselves on creating an inclusive and dynamic workplace that values diverse perspectives and experiences. While we typically welcome applicants from all locations, for this particular role, we are prioritizing candidates who are currently residing close to our offices in Flemingsberg, Lund, Søborg or Kolding. Our commitment to integrity We care about diversity, inclusion, and equity in our recruitment processes. We also believe behavioural traits can provide important insights into a candidate's fit to a role. To help us achieve this we apply Pymetrics assessments, and upon application you will be invited to play the assessment games. As part of Alfa Laval's commitment to a safe and healthy workplace, we conduct background checks on final candidates for this role, and alcohol and drug testing is applied during the pre‑employment process. #LI-CL1

Every day, we get opportunities to make a positive impact-on our colleagues, partners, customers, and society. Together, we're pioneering the solutions of the future and unlocking the full potential of precious resources. Trusted to act on initiative, we challenge conventional thinking to develop world-leading technologies that inspire progress in vital areas, including energy, food, water, and shipping. As we push forward, the innovative, open spirit that fuels our 140-year-old start-up culture and rapid growth also drives our personal growth. So, as we shape a more resourceful, less wasteful world, we build our careers too. About the role As a LifeScience Quality & Validation Lead, you will play a key role in ensuring the quality, compliance and performance of Alfa Laval's Life Science systems. You will own and develop Quality & Validation processes our R&D Life Science systems portfolio throughout the entire product lifecycle-from New Product Development to Existing Product Development. Your mission will be to demonstrate that our Life Science systems and related processes meet defined requirements, industry standards and customer expectations. You will contribute from the early stages of development through product maintenance, working with planning, requirements definition, documentation, testing, qualification and follow-up. Working closely with R&D and other stakeholders, you will help ensure the quality of our products and drive continuous improvement across our processes and solutions. Key responsibilities Create and maintain validation documentation, SOPs, work instructions, test protocols and qualification protocols, including CSV, FAT, IQ and OQ. Manage validation-related change control activities across development and maintenance projects, software activities and testing assignments. Define requirements for software, components, validation and testing in collaboration with R&D, Quality and other key stakeholders. Ensure alignment with relevant industry standards, GMP requirements and pharmaceutical customer expectations. Participate in testing and verification of machine functionality at R&D facilities, Alfa Laval manufacturing sites and subcontractors. Lead internal, external and customer audits, identifying deviations, improvement opportunities, gaps and required actions. Lead risk assessments and define Quality & Validation strategies throughout the product lifecycle, aligned with the Life Science product roadmap. Drive continuous improvement, promote best practices and share knowledge through training, demonstrations, conferences and stakeholder activities. Who you are You are a collaborative and communicative professional who enjoys working with colleagues across different functions, locations and levels of responsibility. You can explain complex topics clearly, both verbally and in writing, and build effective working relationships with internal and external stakeholders. You are curious, structured and solution oriented. You see challenges as opportunities to improve, anticipate potential consequences and take ownership of delivering high-quality results on time. What you know At least five years of experience validating complex systems in the Life Science or pharmaceutical industry. Strong knowledge of GMP and pharmaceutical compliance requirements. Familiarity with computerized system validation (CSV). Experience with risk assessments and risk-based validation approaches. Knowledge of qualification and testing activities, such as FAT, IQ and OQ. An understanding of relevant Life Science regulations, standards and industry guidelines. Excellent communication skills in English, both written and spoken. What's in it for you? This is an opportunity to develop as a Subject Matter Expert and help strengthen Alfa Laval's ability to meet industry regulations and customer expectations. You will have a central role in shaping robust, compliant and reliable Life Science systems while influencing the development of our products, processes and ways of working. You will work with talented colleagues across the organization and have the opportunity to make a tangible impact throughout the product lifecycle. For more information, please contact Fabio Gillué Tomás, Manager Smart Separation Systems Design & Development, Regina García Moguel, Talent Acquisition Partner, Union information Axel Schäring, Akademikerna, Anders Jansson, Unionen, We review applications continually so please send in yours as soon as possible and not later than November 1st, 2026. Please note that, in compliance with GDPR, we cannot accept applications submitted via email. As part of Alfa Laval commitment to a safe and healthy workplace, alcohol and drug testing is applied during the preemployment process. #LI-RG1

Vill du vara med och skapa framtidens arbetsplats? Som Workplace Coordinator på Alfa Laval får du en central roll i att utveckla och erbjuda en innovativ, hållbar och inspirerande arbetsmiljö för våra medarbetare i Ronneby. Du bidrar till att vår arbetsplats fungerar effektivt och kostnadsmedvetet, samtidigt som du driver utvecklingen framåt i linje med verksamhetens mål och vårt starka fokus på hållbarhet. Med service, engagemang och nytänkande skapar du de bästa förutsättningarna för en attraktiv och välfungerande arbetsplats. Arbetsuppgifter: Ge excellent service inom utvalda leveranser inom Workplace Arbeta mångsidigt genom att kombinera olika arbetsuppgifter och serviceområden till exempel: Växel, Reception, Event, Service Point, Telefoni, Office Support samt arbetskläder/skor. Samverka och samarbeta med olika siter inom Alfa Laval Technologies. Dagligt arbete i företagets olika system och digitala verktyg. Föreslå, aktivt bidra samt genomföra kostnadsmedvetna förbättringar med fokus på hållbarhet och kvalitet. Aktivt bidra till kvalitet och ekonomisk uppföljning av våra mål och mätetal Samverka och stödja samarbete för att säkerställa kvalitetssäkrade processer och serviceleveranser i Ronneby. Vem är du? Lösningsorienterad, initiativtagande och öppen för ständiga förbättringar God samarbetsförmåga och serviceinriktad Förmåga att kombinera kundservice med administrativa uppgifter Goda kunskaper i flera serviceområden inom Workplace serviceportfölj God systemvana (MS Office-365 och administrativa verktyg) God förmåga att kommunicera och uttrycka sig i tal/skrift både på svenska och engelska För mer information om tjänsten kontakta Robin Zickbauer, Facility Team Manager, +46709366509 Facklig information Ulf Johansson, Unionen, +46733975607 Som en del i Alfa Lavals arbete för en säker och hälsosam arbetsplats tillämpas alkohol och drogtestning vid nyanställning. Välkommen med din ansökan senast den 7 november 2026. Rekrytering sker löpande och tjänsten kan tillsättas före sista ansökningsdag.