Cytiva Sweden AB jobb i Uppsala

Bli del av något större
Är du redo att ta din potential till nästa nivå och göra verklig skillnad inom Life Science, diagnostik och bioteknik?
På Cytiva, ett av Danahers 15 dotterbolag, räddar vårt arbete liv. Hos oss blir du del av en kultur som präglas av gemenskap och tillhörighet där ditt unika perspektiv spelar roll. Med hjälp av Danaher Business System omvandlar vi idéer till konkreta lösningar.?
Att arbeta på Cytiva innebär att ligga i framkant av att utveckla nya sätt att förbättra människors hälsa. Våra kunder bedriver allt från grundläggande biologisk forskning till att utveckla innovativa vacciner, nya läkemedel och cell- och genterapier.
På Cytiva får du chansen att utvecklas tillsammans med oss och göra verklig skillnad för människor världen över. Ta chansen att bli del av något större.
Läs mer om Danaher Business System som gör allt möjligt.?
Vi söker nu efter en Scrum Master / Team Lead till avdelningen för Downstream Software R&D. Som Scrum Master / Team Lead på Cytiva ansvarar du för att leda ett nyformat mjukvaruutvecklingsteam som tillsammans med angränsande team och funktioner arbetar för att leverera mjukvara till våra kromatografisystem. Du kommer att säkerställa att ditt team har förutsättningar att kunna leverera som ett engagerat och högpreseterande team där medarbetarna samarbetar effektivt för att kunna leverera i våra projekt.
Vidare kommer du att arbeta med att finslipa våra arbetssätt inom teamet, avdelningen och våra utvecklingsprojekt. Du kommer dessutom att vara en integrerad del av ditt team och supportera medarbetarna löpande i utveckling, testning, planering och/eller dokumentation av teamets arbetet, beroende på din bakgrund och kompetens. Tjänsten är en tillsvidareanställning och är förlagd onsite på vår site i Uppsala.?
Dina arbetsuppgifter:
Leda teamet inom agila metoder och driva kontinuerliga förbättringar inom teamet och avdelningen.
Jobba för att skapa hög psykologisk trygghet i teamet, så att det blir naturligt för teamet att hjälpas åt att leverera mot uppsatta mål.
Utveckla ett starkt samarbete med andra utvecklarteam och med ledningsgruppen.
Coacha och stötta produktägare i hantering av backlog.
Dela ansvaret för teamets totala prestation, kontinuerligt mäta och förbättra flöde, kvalitet och kundvärde.
Bidra till utvecklingsarbetet i teamet efter kompetens.
Samarbeta med kollegor internationellt.

Vem är du:
Vi söker sig som har ett stort intresse för mjukvaruutveckling och tilltalas av att ta fram helhetssystem som hjälper forskare och läkemedelsutvecklare i deras vardag. Vi söker dig med god förståelse för agila metoder, för projektarbete och för hur man bygger effektiva team. Vi ser gärna att du är trygg både i din tekniska kompetens och i din förmåga att leda team, samt att du är bekväm i att samarbeta med andra för att hitta lösningar och nå resultat.
Högskoleutbildning inom relevant område (t.ex Software Engineering, Computer Science, Molekylär Bioinformatik eller liknande).
Erfarenhet av mjukvaruutveckling med tonvikt på C#/.NET.
Erfarenhet av produktutveckling och kunskap produktlivscykler.
Vi ser gärna att du har erfarenhet av utveckling av mjukvara som en del av ett helt system, där hårdvara och elektronik är en del
Erfarenhet från tidigare roller som Scrum Master, Team Lead och/eller delprojektledare.
Demonstrerad erfarenhet av att jobba driva och implementera förbättringar av arbetssätt och ett agilt mindset i verksamheter.
God vana att jobba inom ramarna för ett kvalitetssystem och en förståelse för dess vikt för att säkerställa plattformens framtida kvalitet.
Kommunicerar flytande i tal och skrift på både svenska och engelska

Stor vikt kommer att läggas vid den ansökandes personlighet, professionella intressen och driv. Vi ser gärna att du som söker är en person med stort intresse för både människa, teknik och organisation. Vi söker dig som känner igen dig i bilden av en prestiegelös och engagerad medarbetare med god problemlösningsförmåga. Arbetet inom avdelningen präglas av samverkan med andra på och utanför avdelningen och det är därför viktigt att du som söker är en utmärkt lagspelare med god samarbetsförmåga som trivs med att arbeta i team för att uppnå bästa möjliga resultat.
Om du är intresserad, vänta inte med att skicka in din ansökan, då vi går igenom ansökningarna löpande. Om du har ytterligare frågor angående tjänsten, kontakta rekryterande chef; Therese Eriksson på thereseeriksson@cytiva.com eller 072 – 145 01 82, eller Ulrika Öhman Öhman på ulrika.ohman@cytiva.com eller 076 – 496 06 55.

Be part of something altogether life-changing
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Lead Software Engineer for Cytiva is responsible for Design and Development of Service Platform & Products to enable remote troubleshooting and diagnostics.
This is a senior technical leadership position and is part of the Global Service R&D Organization located in Uppsala, Sweden and will be an onsite role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Work with global teams on new product development projects to drive Design for Service, Serviceability standards, Predictive and condition-based maintenance strategies adopted by Cytiva through digital connectivity, Data enablement and IoTs.
Work with global teams on new product development projects to define and standardize data collection, storage and export of machine data in a controlled and secure way.
Leverage digital technologies to improve serviceability, remote diagnosis and troubleshooting.
Drive strategic and tactical decision making from a technology perspective; including software modernization.
Design and develop client-server software utilizing MVC, C++, C# .NET, WPF/ WCF and RDBMS, HTML.
Mentor, train and lead developers in line with project objectives and priorities.
Configure and maintain development and deployment environments if needed with the Cytiva DevOps Engineer.

The essential requirements of the job include:
Degree in Computer Science or Software Engineering (or equivalent qualification).
8+ years of experience in commercial software development with hands-on experience in C# / ASP.Net.
Proven understanding of digital technologies and their application in the service/Biotechnology industry.
Experience using Web technologies (e.g. TypeScript/JavaScript, CSS, HTML5, Node.js, or frameworks such as Angular or React).
Experience using Cloud back-end technologies such as Microsoft Azure or AWS.
Database applications using Postgre, Server or similar.
Flexible approach to problem solving with a sense for technical pragmatism and a strong focus on delivery, without sacrificing quality.

It would be a plus if you also possess previous experience in:
Knowledge of electromechanical design, lab scale and industrial hardware systems.
Experience in Continuous Delivery (CD).
GMP & regulatory environments.
QMS and Documentation Practices.

Interview and selection will happen continuously and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Manoja Prabhu at manoja.prabhu@cytiva.com. We look forward to hearing from you!
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
The Scientist is responsible for application research within the capture field, with focus on monoclonal antibody purification processes. The Scientist is a part of a committed and talented team that are highly involved in new product development. To succeed in this position, you need to be result-oriented, flexible and creative with a strong collaborative attitude, focusing on the customer needs. You are eager to learn and try new things with the drive and capability to initiate, plan, perform, analyze, document and present results.
This position reports to the Senior Manager Capture Application and is part of the Start to Finish department within R&D located in Uppsala and will be an on-site role. We are looking for candidate who can join us after the summer, earliest starting date in July 2025.
What you will do:
As a Scientist you will be part of a team working with different steps in a mAb purification process, i.e. clarification, filtration and purification. Also analysis will be included in your work in our different project types, that is new product development but also market support related activities.
Although most work will be performed at lab scale you will also be involved in harvesting and filtration of feed in larger scale.
The work is independently planned and performed and reported at project meetings and in technical reports.

Who you are:
You have a PhD with some experience from chromatography work in the biopharmaceutical field.
Experienced of using ÄKTA systems and multiple analysis methods (ELISA, SEC and BiaCore).
It’s meritorious if you have worked with large scale purification equipment and processes with mAb or recombinant proteins. Experience of filtration of biomolecules would be appreciated.
Advanced English (oral and writing) and working proficiency in Swedish language.



Travel, Motor Vehicle Record & Physical/Environment Requirements:
Valid Swedish work permit.



Application
We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application. The recruitment will be completed as soon as a suitable candidate is found.
We look forward to seeing your application.

Beskrivning av jobb
Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciencesföretag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Vi söker en processingenjör till Cytivas interna reningsverk på vår site i Uppsala. Sektionen Reningsverk & Miljö ingår i Site Business Support (SBS) och ansvarar för sitens luftemissioner, fabriksavloppsvatten och servar därmed hela vår produktionsverksamhet i Uppsala. Sektionen ansvarar för drift och tillgänglighet för reningsanläggningar, utföra mätningar av luft- och vattenemissioner och säkerställer efterlevnad på våra krav på utsläpp.
Vad du ska göra
Arbetet består av att arbeta aktivt med emissioner till luft och vatten från fabriksavloppet som kommer från våra fabriker. I rollen som processingenjör hos oss kommer du arbeta med att supporta den dagliga driften av reningsverket genom provtagning och analys, vara delaktig vid felsökning samt utveckling av reningsanläggningen. Du kommer även att, tillsammans med övrig produktionspersonal, verka för minskade emissioner, trendning av data samt delta i projekt rörande kapacitetsökningar.
Stödja operativ personal med drift, felsökning och metodförbättringar.
Utredning, utveckling och optimering av reningsprocesser för luft och vatten.
Trendning och analys av data rörande emissioner till luft och vatten från produktionen.
Utbilda personal inom produktionen för att öka medvetenheten runt emissioner.
Arbeta med reducerande åtgärder av emissioner till luft och vatten samt följa upp effektiviteten av åtgärder.
Driva change control ärenden, MOC (Management of Change) och riskanalyser inom reningsverkets ramar.
Idka ständigt förbättringsarbete i alla steg inom verksamhetsområdet.
Samarbeta tvärfunktionellt med personal från produktion-, R&D- och EHS-avdelningarna.
Även arbete i andra projekt rörande miljöfrågor i produktionen för att minska påverkan på yttre miljö.

De huvudsakliga kraven för tjänsten är:
Teknisk högskoleutbildning eller annan relevant utbildning med inriktning mot kemi, bio-/kemiteknik, miljö alternativt motsvarande arbetslivserfarenhet.
Erfarenhet från liknande roll, gärna inom processindustri med teknisk inriktning.
God kommunikationsförmåga samt utmärkta kunskaper i svenska och engelska, såväl muntligt som skriftligt.

Det är även meriterande om du har tidigare erfarenhet av:
Erfarenhet av att driva tekniska projekt inom processrening.
Kunskap om reningsprocesser i storskalig kemisk produktionsverksamhet.

Vi ser gärna att du som söker är driven och ansvarstagande med god förmåga att självständigt kunna ta initiativ och fatta beslut. För att vara framgångsrik i rollen är det även viktigt att du som peär förändringsbenägen, har god problemlösningsförmåga och trivs med att jobba både i grupp och självständigt.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag.
#LI-HJ2
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Bring more to life
Är du redo att accelerera din potential och göra verklig skillnad inom biovetenskap, diagnostik och bioteknik?
På Cytiva, ett av Danaher’s 15+ operativa företag, räddar vårt arbete liv – och vi är alla förenade av ett gemensamt engagemang för att förnya för påtaglig effekt.
Du kommer att trivas i en samhörighetskultur där du och din unika syn är viktig. Och genom att utnyttja Danahers system för ständiga förbättringar hjälper du till att omvandla idéer till genomslag – innovativa i livets hastighet.
Att arbeta på Cytiva innebär att ligga i framkant när det gäller att tillhandahålla nya lösningar för att förändra människors hälsa. Våra otroliga kunder genomför livräddande aktiviteter som sträcker sig från grundläggande biologisk forskning till att utveckla innovativa vacciner, nya mediciner och cell- och genterapier.
På Cytiva kommer du att ständigt kunna förbättra dig själv och oss – arbeta med utmaningar som verkligen betyder något med människor som bryr sig om varandra, våra kunder och deras patienter. Ta ditt nästa steg till en helt och hållet livsförändrande karriär.
Lär dig om Danaher Business System som gör allt möjligt.
Site Service Coordinator är ansvarig för att tillhandahålla labrelaterat förbrukningsmaterial inkl service och tjänster kopplat till gas, farligt gods skeppningar samt internorderhantering
Denna position rapporterar till Manager Site Service och är en del av vårt Facility Management team placerad i Uppsala, Sverige och kommer vara en on-site roll.
Vad du ska göra
Serva siten med material/utrustning för laboratorieverksamhet (inkl lagerhållning)
Farligt Gods hantering inkl skeppning farligt gods
Kvävetjänstfyllning NMR & fyllning återvunnet, Pilot Plant
Löpande internorderhantering & registervård av lagersystem
Administrera internrekvisitioner
Etanolredovisning
Bistå Driftcentralen med gas- och inköpsärenden

Vem du är
Dokumenterad erfarenhet av Farligt Gods hantering samt skeppning (IATA, ADR)
Goda kunskaper i svenska och engelska, både tal och skrift
Van datoranvändare med erfarenhet av att arbeta i digitala verktyg och system

Vi ser gärna att du är
Kommunikativ och lösningsorienterad
Säkerhetsmedvetenhet
Har förmåga att bedriva ett organiserat och strukturerat arbete



Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. Varmt välkommen med din ansökan!
Cytiva, ett Danaher-operativt företag, erbjuder ett brett utbud av omfattande, konkurrenskraftiga förmånsprogram som tillför värde till våra liv. Oavsett om det är ett hälsovårdsprogram eller betald ledighet, bidrar våra program till livet utanför jobbet. Kolla in våra förmåner på Danaher Benefits Info.

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
As Cyber Security Engineer within the department you will collaborate with other engineers trained in the field to support life cycle management of legacy products and the development of new products. You will work with the team to create threat models, assess vulnerabilities and together with stakeholders such as product managers decide and execute actions as appropriate.
The role needs to work very horizontal both within R&D and outside with other functions such as service and product management.
This position reports to Sr Manager Magnus Emerius and is part of the ÄKTA Instrument Engineering Section under the Systems Department at R&D located in Uppsala, Sweden and will be an on-site role.
What you will do:
Ensure our products comply with new Information Security standards and frameworks, and best practices for product security, such as NIST SP 800-53 and IEC 62443.
Work with incident response investigations, corrective actions, and preventive actions.
Design of secure systems including secure solutions for embedded software.
Ensure secure configuration, installation and deployment for Windows and Linux.
Threat modelling based on STRIDE.

Who you are:
Master’s degree in engineering or technical discipline or equivalent experience.
Documented education or training in the field of cyber security, or equivalent experience.
Experience from working with threat modelling and risk analysis.
At least 3-5 years of experience working with system development/R&D.
Fluent in Swedish and English, both verbally and in writing.

Application
We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application before the 14th of February 2025. However the position is filled as soon as we find a suitable candidate.
We thank you for your interest and look forward receiving your application.

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
We have an exciting opportunity for a European Patent Attorney (EPA) to work with our expert Intellectual Property team of twentyfive+ employees across the world. The role will be onsite in Uppsala, Sweden and report into Cytiva’s IP Leader for Hardware Solutions.
As a European Patent Attorney, you will be intimately involved in building and implementing the IP strategy for protecting some of Cytiva’s core product portfolios relating to a range of system platforms and software applications for the bioprocess industry. This will cover all aspects from collaborating closely with R&D and business colleagues in building world class IP protection, to execution of global IP litigations. Do you have a passion for innovation and intellectual property? Then we would love to hear from you.
What you’ll do
Lead IP strategy and portfolio management for assigned business areas to ensure that commercially meaningful and enforceable protection is obtained.
Draft and prosecute high quality patent applications.
Perform freedom to operate reviews and minimize exposure to third party IP.
Support IP aspects of business development, licensing, and Merger & Acquisition activities.
Support EPO opposition proceedings and IP enforcement actions.
Provide IP training to R&D, product and marketing teams.

Who you are
Qualified European Patent Attorney
Technical background in mechanical, electrical, or chemical engineering, physics or equivalent.
Excellent written and oral communication skills in English. Proficiency in other languages is considered a plus.
Experience of devising innovative IP strategies.
Good commercial awareness.
Knowledge of laws, regulations, practices and procedures relating to patent procurement in Europe, US and Asia.
Preferably, experience working in the life sciences or healthcare sector.
Valid working permit for Sweden.



Interviews and selection will happen continuously. Welcome in with you application!

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
The "Field Application Scientist - EMEA" position for Cytiva provides technical expertise to sales representatives, resellers and customers during the sales process and works directly with customers.
This position reports to the Manager of Field Application Scientists and is part of the Genomic Medicine division in Europe and will be fully remote. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to
Pre-sales: Play an active role within the commercial team, to promote Cytiva Nano Medicine line of products, manage leads and prospects, develop opportunities, contribute to team spirit, and improve account penetration. Attend and provide high level technical expertise at trade shows and conferences. This role should be able to evaluate a customer's process to identify solutions and provide the?necessary tools, information and support to obtain additional sales and identify new opportunities.
Develop and maintain positive relationships with customers, especially focusing on a network of key decision makers. As a team, set quarterly priorities in your territory to achieve defined business goals.?Contribute to key account plans managed by the Account Management team.
Develop a strong working knowledge of Cytiva Nano Medicine products and services, a detailed understanding of applications utilized by our customer base, as well as a strong working knowledge of the features and benefits of competitive products. Sustained evaluation or awareness of competitor activities and innovations within the marketplace generally. Develop a working knowledge of funding, market dynamics & end-user needs. Provide/facilitate efficient communication on strategic and competitive customer feedback to Marketing and Product Development teams.
Coordinate and conduct on?site and in?house customer training courses. Provide technical sales support by conducting applications?based seminars and product demonstrations. Provide applications / technical training to the sales team.
Provide phone, email, and in?person customer applications support, including troubleshooting issues related to user's technical skills, application, and instruments. Interpret customer needs and identify if the responsibility for a problem resolution falls to sales personnel, engineering, or other company personnel.

The essential requirements of the job include:
Master's Degree in biotechnologies, genomic medicines, nanomedicines OR equivalent field experience.
3+ years of applications or lab experience in a nanoparticle formulation, drug delivery, or cell biology required. Skilled in troubleshooting instrumentation, and applications.
Demonstrated superior problem solving and interpersonal and account management skills in a commercial environment. Demonstrated aptitude towards the selling process and a proven team player. Understanding of customers’ key business drivers. Ability to work independently and a self-starter with a drive for customer satisfaction.
Strong communication skills and experience delivering scientific presentations. Demonstrated technical writing ability.

Travel, Motor Vehicle Record & Physical/Environment Requirements ?:
Must be able to travel 50% in Europe

Preferred:
PhD preferred.

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
As a result of our growing customer needs to ensure maximum lifecycle utilization of their equipment, we are looking for a Global Services Upgrade Engineer/ Technical Services Project Engineer.
The Global Services Upgrade Engineer will be responsible for managing custom upgrade orders. This includes reviewing order, creating part numbers and a build of materials, sourcing the material, engineering the upgrade, and putting instructions together on how to execute the upgrade in the field.
This position reports to the Sr Manager,Global Services Custom Products and Repair Center Operations and is part of the Customer Support Multifuction department located in either Uppsala or Umeå, Sweden and will be an on-site role.
What you’ll do:
Review customer orders for upgrades and determine whether the upgrade is possible.
Create a quote and price proposal to customer
Put together a build of materials for each upgrade and sending a quotation to the requester for the upgrade.
Manage the upgrade projects through installation and making sure the projects runs smoothly.
Maintain appropriate relationships and work with both internal and external suppliers to get pricing and material for each upgrade.
Assemble and quality check each upgrade before sending to the customer.
Write any needed documentation for the field team to execute the upgrade at the customer site.
Handle any customer complaints which come in regarding upgrades delivered.
Work closely with our manufacturing and align resources needed to deliver upgrades.
Ensure regular communication to key stakeholders and end users (Service Managers/Field Engineers)
Develop and maintain quality-controlled processes/SOPs
Upgrade support to customer and field engineer, travel as needed – 10-15%.

Who you are:
High level of technical knowledge and understanding (hardware/software)
Bachelor of Science/ Engineering or equivalent
5--10 years experience with electrical and automation design and/or in similar role
Strong focus on customer, quality and meeting customer needs in a global environment
Excellent communications skills in Swedish and English (oral and written)
Proficient in Microsoft Office applications

Interviews and candidate selection will happen continuously, we look forward to your application today!
Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta utvecklas i din karriär och stärka dina färdigheter över tid.
Vi är en del av Danahers bioteknologisegment och sammanför teknisk expertis och talang från hela världen för att utveckla nästa generations livsförändrande terapier.
Vi vill nu förstärka vårt team i Uppsala med en optikingenjör. Du kommer ingå i en sektion med andra ingenjörer inom optik, men även inom elektronik och inbyggd mjukvara. Hos oss är tillvaron varierande och du kommer att vara delaktig i utveckling och förbättring av våra kromatografisystem. Du kommer att ha stort ansvar i att själv planera och utföra ditt arbete – frihet under ansvar. Arbetsuppgifterna ger, och behöver, teknisk bredd. Låter detta intressant? Då vill vi höra ifrån dig!
I den här rollen kommer du få möjligheten att:
Designa, utveckla och optimera UV-sensorer och optiska system för kromatografi-applikationer.
Utföra optiksimuleringar och analyser med hjälp av Ansys Zemax OpticStudio för att säkerställa hög prestanda och effektivitet.
Genomföra tester och kalibreringar av optiska system för att säkerställa noggrannhet och tillförlitlighet.
Samarbeta med tvärfunktionella team, inklusive elektronik-, mekanik- och mjukvaruingenjörer, för att integrera optiska komponenter i kompletta system.
Dokumentera designprocesser, testresultat och tekniska specifikationer enligt företagets standarder.
Utföra felsökning och problemlösning av optiska system och komponenter.
Hålla dig uppdaterad med de senaste teknologierna och utvecklingsmetoderna inom optik och sensorteknik.
Bidra till projektplanering och tidsramar genom att uppskatta arbetsinsatser och resurser för optikrelaterade uppgifter.

De huvudsakliga kraven för tjänsten är:
Civilingenjör inom teknisk fysik eller motsvarande.
Mångårig dokumenterad erfarenhet av relaterad produkt- & systemutveckling.
Stark problemlösningsförmåga och förmåga att arbeta i team.
Flytande i svenska och engelska i såväl tal som skrift.

Det är även meriterande om du har tidigare erfarenhet av:
Optik och fotonik med hjälp av modellering och simuleringar.
Spektroskopi och/eller kromatografi.

Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta utvecklas i din karriär och stärka dina färdigheter över tid.
Vi är en del av Danahers bioteknologisegment och sammanför teknisk expertis och talang från hela världen för att utveckla nästa generations livsförändrande terapier.
Vi inom System Support tar ansvar för drift och support av det digitala landskapet inom den kemiska produktionen i Uppsala. Just nu befinner vi oss i en expansion av vår nya digitala plattform som kommer befästa vår världsledande position. Vårt mål är ett landskap där vi till fullo utnyttjar potentialen i vår digitala ryggrad inom produktionen.
Till denna resa stärker vi vårt team med en ny engagerad Systemingenjör.
Teamet ansvarar för ett flertal olika validerade produktionskritiska system. I ansvaret ingår support till användare, systemförvaltning som uppdateringar av system och dokumentation samt deltagande i projekt som subject matter expert. Som systemingenjör är du en viktig del i teamet för att säkra driften och utvecklingen av våra produktionssystem.
Du kommer primärt att arbeta med Snitcher Medical. Ett system vi använder för att utveckla och förvalta etiketter för våra slutprodukter. Det ingår även ansvar för andra system såsom till exempel Boomerang (system för temperaturövervakning).
Vi är mitt i en spännande resa som tar oss in i en digital produktion i världsklass.
I den här rollen kommer du få möjligheten att:
Supportera och utbilda verksamheten samt utföra avhjälpande åtgärder.
Systemförvaltning och uppgraderingar.
Designa och hantera layouter för produktetiketter.
Arbeta med ständiga förbättringar av våra system och interna arbetsprocesser.
Systemintegration.
Upprätthålla systemdokumentation och rutiner

Arbetet är intressant och varierande då du hanterar många ärenden av olika karaktär och kommer i kontakt med många personer både internt och externt. Du ser möjligheter med system som utbyter information i syfte att förenkla, automatisera och säkra kvalitet.
Vi eftersträvar en hög servicegrad varför kommunikation och transparens är viktigt likaså en stor förståelse för våra kunders behov. Självklart sätter du kunden i fokus och är en serviceinriktad person. Det är naturligt för dig att följa upp att pågående aktiviteters levereras samt att tillhörande dokumentation är uppdaterad. Vi ser att du har ett metodiskt arbetssätt och har lätt för att se samband hur olika operationer hänger samman.
De huvudsakliga kraven för tjänsten är:
Examen från högskola eller universitet med relevant inriktning, eller erfarenhet från arbete i liknande roll, eller mångårig erfarenhet som systemingenjör med ansvar för produktionskritiska system.
Ett brinnande intresse för digitalisering.
Erfarenhet från förvaltning av produktionsnära system såsom ERP, MES, asset management eller documentation management. Andra systemerfarenheter är också intressanta.
Livscykelaktiviteter kopplade till system.
Det är naturligt för dig att kommunicera på svenska och engelska.

Det är även meriterande om du har tidigare erfarenhet av:
Systemintegration.
Supportverksamhet och aktiv systemförvaltning.
Produktions IT såsom nätverk, servrar och AD.
Validering av IT system.

Bli en del av något helt livsavgörande
Att arbeta på Cytiva innebär att ligga i framkant vad gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunder ägnar sig åt att ta fram produkter inom en rad områden som sträcker sig från grundläggande biologisk forskning till framtagande av innovativa vacciner, nya läkemedel och cell- och genterapier.
Som del av Cytiva kommer du kontinuerligt förbättra dig själv och oss – du kommer att bidra till att lösa utmaningar som har verklig betydelse för människors hälsa tillsammans med kollegor som bryr sig om varandra, våra kunder och deras patienter.
Med medarbetare i över 40 länder är Cytiva en arbetsplats där varje dag är en möjlighet att lära sig mer – så att du kan fortsätta utvecklas i din karriär och stärka dina färdigheter över tid.
Vi söker nu efter en Software Engineer med erfarenhet av Frontendutveckling till ett av våra mjukvaruutvecklingsteam inom avdelningen R&D BioProcess Software på Cytiva i Uppsala. Avdelningen består idag av ett 90-tal medarbetare som ansvarar för mjukvaruutvecklingen inom affärsområdet BioProcess Downstream. Vår största mjukvara, UNICORN, används av kromatografi-, cellodling- och filtreringsystem för styrning, övervakning och avancerad analys.
I rollen som Software Engineer kommer du att jobba i en dynamisk och agil miljö där du kommer vara en del av ett team involverat i hela utvecklingsprocessen från kravspecificering till implementation och test samt slutligen verifiering. Automatiserad enhetstestning, TDD (Test Driven Design) och BDD (Behavior Driven Design) är en integrerad del av arbetssättet. Tjänsten har placering on-site i Uppsala.
Dina arbetsuppgifter:
Planera och utveckla nya features till våra produkter samt genomföra tekniska utredningar.
Skriva teknisk dokumentation så som mjukvarudesign-, krav- och testspecifikationer.
Underhålla befintliga produkter.
Stötta vårt kundsupportteam med teknisk kompetens om våra produkter samt att ibland ingå i tekniska utredningar av kundproblem.

De huvudsakliga kraven för tjänsten är:
Relevant universitetsutbildning, exempelvis MSc / BSc Software Engineering, Computer Science, eller motsvarande.
Erfarenhet av mjukvaruutveckling med tonvikt på C# / .NET samt WPF / Win Forms.
Vana att jobba inom ett kvalitetssystem.
Du kommunicerar flytande på både svenska och engelska.

Det är även meriterande om du har:
Erfarenhet av TDD (Test Driven Design) och BDD (Behavior Driven Design).
Erfarenhet av produktutveckling och kunskap om produktlivscykeln.
Vana att jobba inom ett kvalitetssystem.
Erfarenhet av agila arbetsmetoder.
Intresse för cyber security och secure coding.

Stor vikt kommer att läggas vid den ansökandes personlighet, professionella intressen och driv.?Vi söker dig som har god analytisk förmåga och ett stort intresse för mjukvaruutveckling. Du är trygg både i din tekniska kompetens och känner dig bekväm i att samarbeta brett och tvärfunktionellt med andra för att hitta lösningar och nå resultat.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande tjänsten vänligen kontakta rekryterande chef Ulrika Öhman, Senior Manager - UNICORN Application Software, ulrika.ohman@cytiva.com. Välkommen med din ansökan!

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
We're looking for a Lead System Designer to join our Custom Engineering department at Cytiva in Uppsala. This position reports to the Sr Manager for Functional Design and will be an on-site role.
As Lead System Designer at Custom Engineering you will be working primarily on customized customer projects together with cross-functional project teams consisting of 8 to 10 people. Each project typically lasts between 6-12 months. In this role, you will take responsibility for the functionality and quality of the customized bioprocess product, including specifications, component and equipment selection as well as regulatory compliance. Your daily activities will be to work closely with the other design disciplines (Mechanical, Automation and Electrical Design Engineering) to ensure that all customer requirements are captured and implemented into the product. At the end of the project, the customer will perform an acceptance test of the equipment at our facility where you will represent the design team and support the customer with technical knowledge.
Cytivas customers are based across the globe, and a few business trips per year may be required as well as some early or late conference calls depending on projects and region.
What You'll Do:
Read customer specifications and translate these into specifications and designs.
Perform design reviews internally and externally together with the customer.
Coordinate design activities between functions (Mechanical, Electrical and Automation design).
Ensure regulatory compliance of your products.
Act as a support function for Service, Manufacturing and Verification.

Who you are:
This position requires an MSc or BSc in Engineering, Physics or Biotechnology, or equivalent.
You have several years of documented experience from working with product development or process development within a regulatory controlled industry or environment.
Experience in performing and/or leading technical investigations and reports (CAPA investigations, component evaluations, etc).
Fluency in English, both written and oral is a requirement. Fluency in Swedish is an advantage.

It would be a plus if you also possess previous experience in:
Knowledge of project management techniques and models.
Experience from technical roles within the Life Science industry.
Experience from working in PDM system.

To be successful in this role, you should have a deep-rooted technical interest, strong quality-focus, and enjoy working in smaller project teams. Excellent communication skills are essential, and you should be comfortable presenting technical solutions to customers.
Interview and selection will happen continuously and an opening can be filled before last day of application. For questions and more information about the role please contact hiring manager Joakim Eklund, Sr Manager - Functional Design, joakim.eklund@cytiva.com.
#LI-HJ2
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Vi söker nu en produktionsplanerare till vår kemiska produktionssite i Uppsala. Som produktionsplanerare hos oss ansvarar du för att sätta produktionsplanen, tillse att material finns tillgängligt för produktionen samt följa upp leveranserna. I rollen ingår även att optimera lager och kapacitetsutnyttjande, vilket ofta drivs i mindre arbetsprojekt. Arbetet förutsätter ett tätt samarbete med många kontaktytor inom såväl produktion, distribution samt marketing, vilket ställer höga krav på noggrannhet, struktur och kommunikativ förmåga.
Vad du ska göra
Hos oss får du möjligheten att arbeta både operativt och strategiskt där ständiga förbättringar välkomnas. Du planerar produktionen i nära samarbete med olika avdelningar.
Skapa produktionsplan för fabriken.
Leda planeringsmöten.
Arbeta med lagerstyrning och optimering.
Ansvara för tilldelning av material.
Arbeta med att förbättra och effektivisera processer.
Följa upp utfallet mot produktionsplanen.

På Cytiva finns goda möjligheter till karriärutveckling och tjänsten kan på sikt utvecklas och formas utifrån din bakgrund och intresseområde.
Vem du är
Vi tror att du har en Ingenjörs eller Civilingenjörsutbildning inom logistik eller teknik eller motsvarande.
Du har erfarenhet av produktionsplanering inom tillverkningsindustrin.
Erfarenhet av ERP-system och goda kunskaper i Excel.
Goda kunskaper i svenska och engelska såväl tal som skrift.
En förmåga att leda och inspirera andra människor.
Du har en serviceinriktad attityd och ett effektivt arbetssätt.
Du har en mycket god kommunikativ förmåga.

Bli en del av något helt livsavgörande
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Nu söker vi en Senior QA Engineer - Projects till sektionen QA Projects på Cytivas QA avdelning i Uppsala. Som Senior QA Engineer representerar du QA i R&D- och siteprojekt med särskilt fokus på valideringsaktiviteter. I denna roll jobbar du tvärfunktionellt tillsammans med medarbetare från bland annat produktion, R&D och PMO. Tjänsten är en onsiteroll med placering i Uppsala.
I den här rollen får du möjlighet att:
Representera QA i tvärfunktionella projekt som nyprodukt- och utrustningsprojekt.
Bidra till att valideringsaktiviteter blir färdigställda inom satta tidsplaner, i nära samarbete med övriga funktioner.
Representera QA i tvärfunktionella riskanalyser.
Remissa och godkänna riskanalyser, valideringsdokumentation och avvikelser.
Aktivt delta i och driva förändringsarbete och ständiga förbättringar inom projekt och processer.
Säkerställa efterlevnad av vårt kvalitetssystem (QMS) i nära samarbete med övriga organisationen.

Grundläggande krav för tjänsten är:
Högskoleutbildning inom kemi, farmaci eller motsvarande.
Flerårig erfarenhet från liknande QA-roller inom reglerad Life Sciencesverksamhet (t.ex ISO 9001, ISO 13485 och/eller GMP).
Erfarenhet av att representera QA i projekt.
Goda kunskaper om validering- och kvalificeringsaktiviteter inom automation, processutrustning och CSV.
Erfarenhet av att driva och/eller representera QA i riskanalyser.
Erfarenhet av att driva och/eller representera QA i avvikelseutredningar.
Du kommunicerar flytande på svenska och engelska i både tal och skrift.

Det är även meriterande om du har:
Goda kunskaper om riskanalysmetodiker.
Erfarenhet av komplexa QA projekt och aktiviteter

Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor relaterade till tjänsten kontakta rekryterande chef Erika Lodén, Section Manager QA - Projects, erika.loden@cytiva.com.

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
The QA Specialist - Quality Management System (QMS) will work closely with the Change Control Process Leader and the CCQA team to drive Change Control errands across the business. In addition, the QA Specialist - QMS will play a key role in supporting other QMS processes and tasks within the wider QA department.
This position reports to the Senior Section Manager - QA Projects, and is part of the Quality Assurance department, Quality and Regulatory Affairs, located in Uppsala and will be an on-site role.
What you will do:
Support the organization regarding QMS related topics.
Review and approve Change Control errands and prepare changes to the Change Control Board (CCB).
Support the Change Control Process Leader with process improvements.
Support other QMS Process Leaders with tasks within the QMS processes, such as assigning QMS trainings.
Review and approve quality events related to deviations and risk assessments.
Work closely with Change Leaders from different parts of the organization, the cross-functional team of certified Change Control QA as well as the Change Control Leader.
Represent QA in cross-functional risk assessments.
Attend Customer Audits to present QMS processes.
Support key quality activities and take on additional tasks supporting the overall performance of the team.

Who you are:
Bachelor's degree in Chemistry, Pharmacy, Engineering, or equivalent.
Prior experience from similar QA roles within the Life Science industry managing Change Control errands, deviations and other QMS related processes.
Knowledge of relevant quality standards and regulatory requirements (e.g., ISO 9001, ISO 13485, GMP).
Ability to communicate effectively in Swedish and English, both written and oral.

It would be a plus if you also possess previous experience in:
Proficient user of Microsoft Office software. Advanced skills in Excel is a plus.
Experience of risk assessments.
Familiarity with Lean, Six Sigma, or other process improvement methodologies.

To be successful in this role, we believe that you are a highly engaged and self-motived individual with excellent networking, interpersonal and communication skills. In addition, we're looking for a structured individual with the ability to work effectively both independently and with others. The ideal candidate should have a service-oriented mindset with quality focus and high integrity.
Interview and selection will happen continuously and the opening can be filled before the last day of application. For questions regarding the role please contact hiring manager Erika Lodén, Senior Section Manager - QA Projects, erika.loden@cytiva.com.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
We are looking for a Research Engineer for our team in Uppsala. You will, as part of R&D, contribute to the development of new products which are used in the manufacturing of leading biological drugs. You will also take active part in trouble shooting of existing Cytiva processes. The Uppsala Cytiva site is the workplace for more than 1500 people including in addition to R&D also functions as manufacturing, marketing, quality control and QA. Cross-functional activities in collaboration with other units will represent an important part of work responsibilities.
This position has a strong focus on hands-on synthesis work in lab scale with focus on development of chromatography resins for bioseparations. Hence the person suited for this opening should enjoy working in a chemistry lab.
What you will do:
Perform experimental work within the area of surface/polymer/organic chemistry with focus on particle generation
Work in science projects as well as product development
Perform primary characterization
Independently plan and accomplish given tasks from Project Manager or Section Manager, to reach given project objectives
Document and report results both orally and written

Who you are:
BSc. Or MSc, or equal experience in chemistry, chemical engineering or similar
1-2 years of work experience in relevant field
Documented laboratory experience
Fluency in English and Swedish, both written and oral communication
Structured and organized team player
Valid work permit

Meritorious:
Experience of work with polysaccharides
Experience from emulsification work
Experience from development of chromatography resins

Interview and selection will happen continuously, and an opening can be filled before last day of application, which is January 20th, 2025.
Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Product marketing Manager for Cytiva is responsible for global marketing programs for Lab scale resins, Imaging & Wb and Impurity ELISa product portfolios at Cytiva.
This position is part of the Discovery business Global Marketing team and will be based on-site in Uppsala but sometimes travel within Europe, UK or USCAN regions. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
What you’ll do
Designs and executes omnichannel lead gen and awareness campaigns for your products to enable funnel additions
Present and maintain your marketing KPIs and targets- leads, funnel additions, funnel wins, etc. and develop counter measures where needed
Identify and lead PSPs where necessary
Create yearly marketing plan for responsible products
Works on and launches NPI projects to deliver target value propositions, messaging, customer VOC, assets for launch, etc.
Write and develop ad & promo materials for your products
Liaise with creative agencies to develop creative concepts/ articles/ etc.
Co-ordinates with marcom to ensure assets needed for campaigns and sales enablement are created and devlivered on time
Works with R&D and technical groups to develop scientific content that resonates with your target customer.



Who you are
Masters degree in marketing or life sciences or related field
Minimum of 3 years experience in marketing/ product management/ marketing communications or other related field
Experience in managing product marketing/ product management for 20-50 MUSD + business
Demonstrated experience in building and executing lead generation and awareness initiatives
Demonstrated experience in developing a strong strategic marketing plan
Able to translate scientific concepts and product features to marketing messages and content that resonate with customers
Demonstrated experience in building content/ creative concepts that speaks to the value of products/ builds storylines that resonate with the need of our customers
Experienced and confident in managing marketing projects (NPIs, customer VOC, etc.)
Comfortable and confident in reporting marketing KPIs to management
Comfortable working in a matrixed environment with cross-functional teams and able to collaborate
Live in the area nearby Uppsala and have the possibility to commute to our site daily.



Nice to have previous experience
Working with/ Knowledge of Lab scale resins or HPLC/ FPLC chromatography systems
Familiar with DBS tools: Transformative Marketing, Launch Excellence and PSP
Able to communicate clearly and effectively with stakeholder
Thrives in a fast paced matrixed environment
Takes ownership and accountability of products and driven to achieve business goals



Application
We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application. The recruitment will be completed as soon as a suitable candidate is found.
We look forward to seeing your application.

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
We are looking for a Fast Trak Scientist to join our Fast Trak team, a global organization within Cytiva that works to support our customers in the biopharma industry.
The Fast Trak Scientist is part of the Fast Trak EMEA team based out of Uppsala, Sweden. We are a dynamic and customer-facing team with great opportunities to develop and grow through a broad variety of process development services for various biomolecules as well as training courses supporting the EMEA biopharma industry. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Focus on chromatography techniques and you will be coordinating activities and working directly with our customers in a dynamic and collaborative environment, acting as subject matter expert.
You will take the role as an expert in discussions with the customer, develop and/or transfer methods and perform experiments during projects.
You will work proactively to contributing to process development projects with creative ideas on how to best solve challenges using already in-place solutions or proposing the implementation of new ones.
Conduct independent scientific work on customer process development projects with monoclonal antibodies, vaccines, recombinant proteins, plasmids etc., including both administrative and laboratory work, both for analytics and bioprocessing.
Deliver training courses for customers, theoretical as well as practical, in the field of biomanufacturing.
To effectively perform the job, you will develop and nurture your internal network within the local and Fast Trak global scientific teams while also securing a creative environment in the customer projects to support and identify successful and scalable solutions for their biomanufacturing processes.

The essential requirements of the job include:
MSc in biotechnology, bioprocess/biomedical engineering or related life sciences field.
Experience working with chromatographic methods (e.g., affinity chromatography, SEC, IEX).
Experience from large scale downstream processes is strongly advantageous.
Experience from analytical techniques such as PCR, electrophoresis and ELISA/SPR methods.
Strong presentation and communication skills. Since working language is English advanced English skills is required both in oral and writing.
A valid EU work permit is required for this role.
Preferably you also have industrial experience in downstream processing of biomolecules or viral vectors.

To be successful in this role, we believe that you are a person who thrives working in a flexible environment with demonstrated abilities to navigate in a collaborative, matrixed, and customer focused environment. You have a strong ability to spot customer needs, communicate solutions and build trust by collaborating to implement effective analytical methods.
Interview and selection will happen continuously, and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Jesper Hedberg at jesper.hedberg@cytiva.com. We look forward to hearing from you!
Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible.
The Bioprocess Development Scientist is responsible for evaluating and optimizing Cytiva filtration technology in biopharmaceutical processes. The BDS advises customers on process options, runs filterability studies, and helps overcome filtration challenges in drug process development. This position is located remotely in Uppsala, Sweden and covers projects in the Nordics and Baltics territory. This position reports to the EMEA Filtration BPS Leader and is part of the BioPharma Process team and will be fully remote.


What you will do:
Engage in technical consultations with customers on downstream filtration processing where you evaluate and propose options for process optimization
Coordinate, perform and analyze bench scale test work at customer site for Cytiva filtration technologies in customer’s biopharmaceutical processes.
Serve as a technical specialist with in-depth knowledge of Cytiva products and downstream processing and develop expertise by regular exchange of experiences and trainings.
Join a dynamic cross-functional and cross-regional team of bioprocess scientists
Work in close relationship with sales specialists, account managers, and scientists to coordinate activities and win sales
Be part of the bringing future biopharmaceuticals to patients by supporting process development of molecules such as monoclonal antibodies, recombinant proteins or vaccines



Who you are:
Master’s Degree in Life Science, Chemical or Biological, or Engineering or related field required, PhD preferred
5 plus years of relevant experience in biotech industry, preferably in downstream process development
Valid driver’s license
Willing to travel regionally (approximately 50%) with occasional travel outside assigned territory
English fluency required, Swedish language a plus

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
What you'll do:
As Senior HR Business Partner at Cytiva, you will be responsible for the short and long-term strategic leadership of all aspects of HR management for the assigned client groups within BioProcess. You will serve as an advisor and counsel to global leadership teams to help them achieve their business goals through effective HR strategy deployment and by providing guidance as needed for effective decision making.
The incumbent will also be responsible for providing leadership and direction to the global and local Human Resource teams supporting the assigned client groups within BioProcess in the acquisition and development of talent as well as creating and maintaining a highly productive and engaging work environment. You will serve as a thought leader and partner in advancing organizational capabilities and effectiveness and will provide lead organizational and talent development efforts to meet strategic and annual business objectives.
Additionally, the Senior HR Business Partner will also focus on developing a culture that facilitates open communication with leadership, advances the Associate value proposition and educates associates on how they contribute to enterprise-wide goals. Key responsibilities include, but are not limited to:
Proactively engage with the leadership team for assigned client groups, acting as a thought partner on business, people and organization-related opportunities to drive business results and build culture.
Determine organizational implications of business strategy; facilitate organizational diagnosis and metrics to drive organizational effectiveness through talent and organizational capabilities and culture.
Partner with local HR and Talent Management to drive annual strategic talent processes.
Assess and identify talent acquisition needs; partner with local HR and Talent Acquisition teams to build talent pools, cultivate talent, identify critical capabilities, etc.
Enable leaders to assess and create talent development opportunities and facilitate cross-functional talent movement.
Assess and identify retention and engagement trends; partner with local HR and Talent Management teams to develop and implement retention and engagement strategies.
Act as an advisor to leaders during times of change and partner with the business to develop and implement change management and communication plans.
Provide coaching and guidance for performance improvement, facilitating difficult feedback and other employee relations support for leaders of assigned client groups. Partner with regional HR teams to identify performance management trends in the organization and identify countermeasures to close gaps.
Act a consultant and advisor on Diversity, Equity & Inclusion to further learning and capability.
Through DBS, identify key targets to improve/metrics to analyze and solve business problems that impact organizational effectiveness. Lead cross OpCo / BU / Regional improvement projects as assigned.
Partner closely with the HR Centers of Excellence (COEs) and Regional HR teams to execute programs, processes and practices, including Performance Management, Retention and Engagement efforts, Learning and Development, Compensation Planning, and Organization Talent Review.

Who you are:
We are looking for a consultative Human Resources professional who is experienced with providing a variety of HR solutions to meet business needs. You love analyzing data, identifying continuous improvement opportunities, and excel in building relationships with business stakeholders in a matrixed, collaborative and an environment.
A Bachelor’s degree in Industrial/Organizational Psychology, Human Resource Management, Business Administration, or a related field.
8+ years of experience in progressive roles in human resources, with prior experience leading a global team.
Demonstrated experience as a cross-functional partner who collaborates well and can indirectly influence in a matrixed environment.
A self-motivated individual who is comfortable operating with minimal direction and who thrives in a dynamic environment as a leader influencing change and transformation.
Credible and savvy business partner who will be perceived as a trusted consultant and functional expert to senior management.
Mission-driven individual with high energy and strong levels of perseverance; works toward both individual and team goals.
Developer of cross-functional HR talent; Committed to elevating the overall HR function.
Demonstrated critical thinking and problem-solving capabilities, and possesses intellectual curiosity, agility, and resourcefulness.
Capable of rolling up one’s sleeves to do what it takes to drive results; not hindered by process or ambiguity.
Willing to travel approximately 20% of the time.

Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Interview and selection will happen continuously, and the opening can be filled before last day of application. For questions regarding the role please contact hiring manager Susanne Spang, Senior HR Director, at susanne.spang@cytiva.com. We look forward to reading your application!

Be part of something altogether life-changing!
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives
We are looking for a Section manager for the Affinity Ligand Design team within the Resin & Ligand Design Department in Resin & Technologies R&D. This section is placed in Stockholm, Solna at Karolinska. The section is responsible for designing new protein affinity ligands and for developing and continuously improving the tools needed for designing these new ligands.


What You'll Do
You will supply Research and Idea evaluation ligand related projects with resources according to the needs in term of time and competences, and secure that deliveries from the section are executed in an efficient and timely manner, and with appropriate quality according to agreed standards.
You will secure that the competence and know-how of the section members is appropriate to support the organization in the field the section is responsible for, and that competences are continuously developed via education, seminars, coaching, mentoring and individual developmental plans.
You will drive the development of the section to improve productivity, establish processes and a strategy to secure long term technology development within the section’s responsibility areas.
You will work in partnership with other Section managers, Project and Program managers and Product management, Marketing and other critical functions.
You will be accountable for the working environment within your team.



Who you are
A strong people leader and experienced in Life Science product development that can balance resources, timing and quality of outcomes.
You have a PhD in biotechnology, biochemistry or related Life Science field or equivalent knowledge or experience.
At least 5 years of experience of industrial development/R&D in the Life Science area
Track record of successful cross-functional collaborations
We are looking for someone with a good ability to motivate, direct and develop people
In order to succeed in this position you need to be motivated, result-oriented, flexible and creative with a strong collaborative attitude, focusing on the customer needs
Live in the area nearby Stockholm and have the possibility to commute to our sites in Solna and Uppsala



Application
We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application. The recruitment will be completed as soon as a suitable candidate is found. We look forward to seeing your application.

Bli en del av något helt livsavgörande
Är du redo att accelerera din potential och göra verklig skillnad inom biovetenskap, diagnostik och bioteknik?
På Cytiva, ett av Danahers 15+ operativa företag, räddar vårt arbete liv – och vi är alla förenade av ett gemensamt engagemang för att förnya för påtaglig effekt. Du kommer att trivas i en samhörighetskultur där du och din unika syn är viktig. Och genom att utnyttja Danahers system för ständiga förbättringar hjälper du till att omvandla idéer till genomslag – innovativa i livets hastighet.
Att arbeta på Cytiva inom Life Science industrin innebär att vara i framkanten när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Våra kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier.
På Cytiva kommer du att ständigt kunna utveckla dig själv och oss - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, våra kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt.
Vi på Cytiva är stolta över att arbeta tillsammans med en grupp av nio andra Danaher Life Sciences-företag. Tillsammans är vi pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv.
Vi söker en Column Engineer som vill jobba med att producera kundanpassade kromatografikolonner.
Den här tjänsten rapporterar till Sr Manager, CDP och är på plats i Uppsala, Sverige. Detta är en tidsbegränsad anställning med start 16 December 2024 till 31 December 2025 eller enligt övernskommelse.
Dina arbetsuppgifter
Som en del i ett team av fyra kollegor kommer du bidra till framtagningen av mestadels kundanpassade kolonner, men även andra typer av labbprodukter - vilka används vid framtagning av läkemedel som till exempel vacciner och cancerläkemedel.
Du kommer ansvara för att, på labb, producera leveranser av kundspecifika produkter och se till att en del av sortimentet finns på lager. Arbetet innefattar också att tillsammans med övriga sektionsmedlemmar planera och strukturera processen, svara på kundfrågor och agera på offerter samt registrering och uppsättning av nya produkter inklusive batchprotokoll, certifikat, och skeppningsdokument.
Du kommer få en bra översikt av stora delar av företaget och arbeta med uppgifter inom produktutveckling och produktion. Som teammedlem i CDP har du kontakt med interna instanser som: Product Management, R&D och även säljorganisationen, vilket gör att du får insyn i kundbehoven och kundens vardag.
Vem är du
Ingenjörsexamen, utbildning som arbetsgivaren bedömer likvärdig eller relevant arbetslivserfarenhet som motsvarar
Minst fem års arbetslivserfarenhet av labarbete, metodutveckling, produktion eller kvalitetssäkring inom Life Science-området
Erfarenhet av Oracle och/eller Magic eller kolonnpackning är meriterande
Du behärskar svenska och engelska obehindrat både i tal och i skrift
Förmåga att arbeta både självständigt och i team
EU arbetstillstånd är ett krav

Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas. Varmt välkommen med din ansökan!

Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Validation and Verification Engineer is responsible for performing verification on time with guidance from senior engineers, planners and project managers according to customer demand.
The Verification section is responsible for planning and execution of functional tests on Bioprocess equipment developed by Custom Engineering.
This position is part of the Verification section in Uppsala and will be an on-site role. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Verification:
Functional testing of Custom engineering equipment.
Support projects to ensure quality and timely delivery of plans and results through daily management.
Support planning and development activities for coming projects.
Participate in customer FATs.
Participate in troubleshooting and suggestion of corrective actions for products, test methods, procedures etc.
Quality inspections of products at sub supplier or at Custom engineering.

Documentation:
Deliver verification documentation and test results.
Participate and or propose development of wow/procedures/methods.

Service/Expertise:
Support training of new resources, secure that GDP and other regulatory requirements are understood and fulfilled.
Support maintenance & development of test facility and test equipment.
Perform installations/troubleshooting at customer site.
Support service with maintenance and repair of customized equipment.
Participate in resolution of case management, CAPA, risk analysis.

The essential requirements of the job include:
Bsc. in mechanical or electrical engineering or similar knowledge from working experience.
GMP knowledge or experience from other regulated business areas.
Experience from testing/verification of operating systems.
Knowledge from Cytiva Bioprocess products.
Fluency in English, both written and spoken.

It would be a plus if you also possess previous experience in:
Fluency in Swedish.

Be part of something altogether life-changing!
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
We are looking for a Finance and Reporting Analyst, RFM to support analytics, forecasting and reporting to RFM (Resin, Filtration, and Cell Culture Media) Finance leaders and CFO.
The individual, as a member of the RFM Finance team, will play a key role in the continuous improvement of our financial processes and is expected to embrace contemporary digital finance capabilities. The role is located in Uppsala, Sweden and will be on-site role.
What you will do:
Lead reporting responsibilities for RFM (Resin, Filtration, and Cell Culture Media) organization including monthly and weekly performance metrics (Bowler), actuals and Forecast summary (Flash Color), and support providing key data for the business summary (President letter).
Lead consolidation of Commercial performance and analyze the data to provide timely business insight for the senior RFM leadership team
Owns forecast and closing process for RFM cost by coordinating with multiple business unit stakeholders and drive cost out initiatives to enhance productivity
Support Business Unit and FP&A Finance leaders by developing and updating operational review templates
Support and own monthly forecasting processes across RFM business units and consolidation of the annual budget; act as a challenge function to business unit finance leads when consolidating and pacing financial performance
Act as the key RFM lead for broader Finance initiatives such as Kaizen, SOX, and IT-Finance and reporting enhancements


Who you are:
Bachelor’s degree in Accounting, Finance, or Business Administration
Minimum of five years of financial work experience, including developing forecasts & operating plans and leading business / finance reviews.
Drivers, generate alternatives and drive positive change
Clear thinking/problem solving: successfully led cross-functional projects/process improvement within operations/finance function; able to quickly grasp new ideas
Solid PC skills: experience with financial systems/applications (i.e.: Oracle, SAP, OneStream, Qlik or other BI tool, etc.), strong Excel skills in data compilation and aggregation (i.e. pivot tables, VLookup, and Macros)

Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.