Sökresultat för "Air Filtration"

Vi expanderar starkt och tryggt mot våra spännande långsiktiga framgångar. Vi välkomnar vår nästa kollegor som projektledare!! Projektledare med erfarenhet inom luftfilter – Borås & Göteborg, Västra Götaland Camfil är världsledande inom luftfilterteknik och grundades för 60 år sedan med visionen "Ren luft är en mänsklig rättighet". Idag är vi nästan 6000 kollegor över hela världen, och hållbarhet är i vårt DNA eftersom våra luftfilterprodukter skyddar människors hälsa och sparar betydande energi. [www.camfil.com) Sammanfattning Tillsammans med vårt projektledningsteam förväntas du på ett tryggt och stabilt sätt, med hjälp av interna resurser och ibland med tredjeparter och leverantörer säkerställa problemfritt genomförande av projekt. Du kommer att säkerställa att projekt levereras i tid, inom omfattning och inom budget. Du kommer att hantera och utveckla projektomfattningar och mål, involvera alla relevanta intressenter och säkerställa teknisk genomförbarhet, varför kommunikationsförmåga är avgörande samt att manövrera i ett matrislandskap både internt och externt. Dessutom kommer du att behöva riskhantera och äga det fullständiga projektets dokumentationsansvar. Du skall ha tidigare erfrarenhet inom vår bransch – air filtration - för denna roll. Vad kommer du att göra – Sammanfattning ansvarsområde I denna roll kommer validering, granskning av standarder och kundspecifikationer att vara väsentliga. Vi tror att du har väl etablerad förmåga för tidsestimat, och organisationsförmågor, samt förståelse för operativa, projektutkast/standarder och olika affärserbjudanden etc. Kombinationen av noggrannhet och affärsförståelse pragmatism, när du hanterar och leder ditt projekt i korrelation med kundkrav, blir avgörande. Som en del av vår internationella matrisorganisation kommer du till exempel tillsammans med tvärfunktionella kollegor interagera kontinuerligt för att förbättra affärsprojekt – både innehåll och effektivitet baserat på "lärdomar" tillsammans. Du kommer på ett sömlöst sätt att verka inom CPS-teamet globalt, med löpande kundinteraktion. Detta i sin tur, kräver kommersiellt intresse, förståelse och utmärkta kommunikationsförmågor, i ett mångkulturellt landskap, för leverans i tid och kvalitetsarbete. Målet är att uppnå robusta marknadskonkurrenskraftiga och kostnadseffektiva lösningar för våra kunder. Vad vi erbjuder För rätt kandidat erbjuder denna roll möjlighet att bidra och växa som teammedlem/medarbetare, såväl som individuellt, i en globalt konkurrensutsatt spännande miljö, på rättvisa och marknadskonkurrenskraftiga villkor. Denna roll kommer att erbjuda en stor känsla av frihet som kommer med ansvar, med breda ramar givet att målen uppnås över tid. Vi erbjuder också - och är säkra på att du kommer att finna både rolig och spännande utveckling i att arbeta på Camfil! Vad kommer att göra dig framgångsrik? För att du ska vara framgångsrik, stimulerad och utmanad tror vi att du har en positiv lösningsorienterad "kan-göra" attityd, en personlig och kommersiell drivkraft. Som individ hoppas vi att du är ivrig att både lära och bidra med en stor team-spirit. Vi hoppas och tror att du är en utmärkt relationsbyggare med förmågan att vara trovärdig på olika senioritetsmässiga nivåer och forum. Vår atmosfär är "opretentiös", varför en självgående förmåga, prioritera arbetsbelastning och hantera tvetydighet kommer att vara mycket användbar och uppskattad. Vi arbetar – vinner och förlorar – som ett team, både lösnings- och målorienterat mot våra ibland utmanande mål/mål. Detta utesluter på intet sätt individuell ambition, entreprenörskap eller global professionell utveckling – tvärtom! Kvalifikationer Vi tror att du har examen såsom civ. ingenjör, maskinteknik eller motsvarande. Du bör ha dokumenterad framgångsrik totalt minst två (2) års erfarenhet som projektledare – eller motsvarande dokumenterad erfarenet inom branschen luftfilter, inom en internationell miljö med solid teknisk bakgrund, med förståelse eller praktisk erfarenhet. Du skall ha tidigare erfrarenhet inom vår bransch – air filtration - för denna roll. Goda skriftliga och muntliga kommunikationsförmågor på engelska och svenska är värdefullt. Låter detta intressant? Då bör du ansöka så snart som möjligt. Om du har frågor är du välkommen att kontakta VP People & Culture, hannes.vedin@camfil.com . Välkommen att skicka din ansökan inklusive brev och CV ! Urval och intervjuer kommer att pågå och tjänsten kan tillsättas före sista ansökningsdatum, så skicka in din ansökan så snart som möjligt! Välkommen med din ansökan!

Are you passionate about combining finance expertise with digital solutions? Do you enjoy working in a global environment where you play a key role in ERP implementations and shaping how financial processes are executed worldwide?  About Nederman  At Nederman, we are proud to be a global leader in industrial air filtration and clean air solutions. We bring together global expertise, engineering, product development, innovation, and digital capabilities in a modern and collaborative environment. It is a place where long-term industrial experience since 1944 meets modern digital development, and where the work you do has a direct impact on real-world operations across Nederman companies globally  What you can expect  Based at our headquarter in Helsingborg, you will be part of a modern and collaborative environment where global expertise meets local team spirit. You will build a strong global network and collaborate with colleagues worldwide.   You will be part of the Nexus team (~20 colleagues) and work with a growing Super User network (100+ users). With an ambitious roadmap and cloud platform, you will continuously learn and develop.  A global ERP program – Nexus  Nexus is our global ERP program implementing IFS Cloud and standardised processes across Nederman companies worldwide, following a structured rollout model from initiation to go-live and hypercare.  What you will do  Drive ERP rollouts from analysis to go-live  Design and configure ERP solutions based on business and technical requirements  Own the module backlog together with business leads  Facilitate workshops and plan work in a structured way  Ensure solution quality, performance, and readiness  Drive documentation, training, and Super User enablement  Act as a change leader towards global processes  We believe you have  Experience within Finance (controlling, accounting or similar)  Experience working with ERP systems (IFS preferred, others relevant)  Experience from ERP implementations or transformation projects  Experience facilitating workshops and planning work  Strong communication skills in English and Swedish What we offer you  A key role in strategic global transformation, a strong international network, continuous development opportunities, and a modern workplace in Helsingborg.   Apply now - Join us in shaping the future of supply chain at Nederman.  We apply continuous selection, so don’t wait to submit your application.For questions, please contact  Nathalie Malmholm,  Manager Business Execution, Nederman Group IT nathalie.malmholm@nederman.com

We're looking for a passionate and driven Senior Manufacturing Scientist – Aseptic Processing to join our Manufacturing Science & Technology (MS&T) team in Uppsala and play a critical role in ensuring the robustness, compliance, and continuous improvement of our aseptic manufacturing processes. At Galderma, we're not just offering a job, we're inviting you to be part of something bigger. About the Role You serve as the site's subject matter expert for aseptic manufacturing and contamination control, providing scientific and technical leadership across critical aseptic operations. You work cross-functionally to support routine operations, troubleshoot complex process challenges, lead investigations, and drive continuous improvement. A key part of the role is leading the site's media fill program and contamination control strategy, and ensuring compliance with evolving regulatory expectations, including EU GMP Annex 1 and global health authority requirements. Key Responsibilities Provide scientific oversight and technical expertise across aseptic manufacturing operations, including compounding, filtration, and filling processes. Lead the site's media fill / Aseptic Process Simulation (APS) program: design, execution, evaluation, reporting, and timely CAPA implementation to strengthen sterility assurance. Lead and support the Contamination Control Strategy (CCS) through scientific risk assessments spanning facility design, HVAC, environmental monitoring, cleaning and disinfection, and aseptic practices. Lead complex deviation investigations, root cause analyses, and CAPA activities related to aseptic processes. Design and evaluate smoke studies to verify airflow performance and first-air protection. Act as a trusted SME in audits, inspections, technology transfers, process improvements, and the implementation of new manufacturing technologies. The role is based at Galderma's production site in Uppsala and requires on-site presence up to four days per week. Your Profile You're a curious, proactive, and scientifically minded professional who enjoys solving complex challenges and driving improvement in highly regulated manufacturing environments. You take ownership naturally, influence stakeholders with confidence, and navigate complexity while keeping compliance and continuous improvement front of mind. Qualifications Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline, with several years of experience in a biopharmaceutical or other highly regulated manufacturing environment. Strong expertise in aseptic processing, contamination control, media fills, and sterility assurance principles within GMP-regulated operations. Experience with EU GMP, Annex 1 requirements, and regulatory expectations for sterile manufacturing. Proven track record leading deviation investigations, root cause analyses, and CAPA implementation. Excellent analytical, problem-solving, and technical writing skills. Strong stakeholder management and collaboration across multiple functions. Ability to independently manage complex projects and drive continuous improvement initiatives. Application If you believe this can be a right career change for you, please send in an application as soon as possible. We are evaluating the application continuously so please do not wait to send in your application. About Galderma Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare, and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ, the skin, meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Our site in Uppsala is Galderma's Global Center of Excellence for Aesthetics, home to over 800 professionals working across R&D, manufacturing, clinical development, and commercial functions. Here, cutting-edge science meets world-class manufacturing, creating an environment where innovation moves rapidly from concept to patient impact. As a Senior Manufacturing Scientist – Aseptic Processing, you'll influence critical manufacturing processes, contribute to regulatory excellence, and play a direct role in delivering high-quality products to patients around the world, joining a collaborative and highly skilled team where your expertise is valued and your ideas are heard.

Role purpose You will work together with our project team as an owner for Mechanical design -taking a data-centre project from early concept through detailed design, procurement, construction support and handover, while staying aligned to EcoDC’s reference architectures and governance. You’ll lead technical due diligence (TDD) for mechanical scope, drive vendor selection, and make pragmatic trade-offs across performance, resilience, maintainability and cost. What you’ll own ·        End-to-end mechanical fitout workstream plan, deliverables and decision log ·        Mechanical interfaces across electrical power, controls/BMS, fire/life safety, water, structural and civil ·        TDD responses for mechanical scope with traceable assumptions and evidence ·        Equipment and vendor strategy: specifications, bid evaluations, clarifications, FAT/SAT input ·        Design issue resolution during construction (RFIs, changes, non-conformance, risk mitigation) Key responsibilities ·        Lead the mechanical design from early phase through construction, ensuring outputs are buildable, operable and maintainable ·        Produce and defend mechanical design decisions (topology, redundancy, water strategy, modularity, control philosophy) ·        Translate customer requirements into robust fitout solutions, including options analysis and cost/benefit trade-offs ·        Write technical specifications and RFQs for major mechanical packages; run structured bid evaluation and clarification processes ·        Act as technical representative with suppliers: clarification logs, performance criteria, testing/acceptance inputs ·        Maintain strong control of scope: identify design risks early, prevent technical scope creep, drive closure to decisions ·        Operate effectively in Nordic delivery environments: clear cadence, transparent communication, fast decisions with good rationale Typical mechanical scope (indicative) ·        Cooling plant and distribution (air and/or liquid cooling infrastructure) ·        Heat rejection and water-side systems, pumping, pipework, valves, filtration/water treatment ·        In-room/white space mechanical fitout and airflow strategy ·        Controls integration (BMS/controls philosophy), alarms, commissioning readiness inputs ·        Maintainability, access, service strategy and operational handover requirements Key interfaces ·        CTO / technical governance (alignment to principles, waivers where needed) ·        Electrical technical lead (power availability, resilience, interfaces, sequencing) ·        Controls/BMS stakeholders (control intent, integration approach, commissioning strategy) ·        Project/construction leadership (schedule, risks, changes, installation constraints) ·        Procurement and key vendors (technical packs, evaluation, testing/acceptance criteria) What good looks like in the first 90 days ·        Mechanical workstream plan established with dependencies, interfaces and decision gates ·        TDD responses delivered with strong traceability, timely closures and minimal rework ·        RFQ/spec packs issued for priority packages; bid evaluation framework running cleanly ·        Clear interface agreements with electrical/controls/fire/water/structure, with no “surprises” late in design ·        Practical construction support cadence in place (RFI triage, change control, issue resolution) Experience and capabilities ·        Proven ownership of mechanical design on mission-critical projects (data centres strongly preferred) ·        Deep mechanical discipline expertise and confidence leading technical reviews and design decisions ·        Strong procurement and vendor management experience (specs, bid evaluations, technical clarifications) ·        Evidence-led communication: assumptions, calculations, options and rationale that stand up in review ·        Calm, structured problem-solving under schedule pressure; comfortable in high-stakes trade-offs ·        Strong collaboration style across multi-discipline teams and site delivery stakeholders