Uppsala: Project Manager – Enterprise Commissioning And Qualification EMEA

Hitta ansökningsinfo om jobbet Project Manager – Enterprise Commissioning And Qualification EMEA i Uppsala. Är det intressant kan du gå vidare och ansöka jobbet. Annars kan du klicka på arbetsgivaren eller yrkesbenämningen för att se alla jobb i Uppsala inom den kategorin.

Publicerad: 2023-03-27 // Varaktighet: Heltid

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.


What you’ll do
Project Management for FlexFactory C&Q.
Be at customer's site during the FlexFactory C&Q.
Develop and improve processes around C&Q in coordination with Enterprise Solutions C&Q Leader and other Enterprise Solutions teams
Coordination of resources and cross functional activities as needed to meet project deadlines.
Support delivery of C&Q plans and related documentation per customer specific project plans.
Drive customer satisfaction and product quality improvements; address manufacturing / field issues to proactively prevent quality issues
Deliver presentations to Customers, Service personnel and Sales teams.
Participation in audits performed by our customers as appropriate



Who you are
Bachelor’s degree in technology, biotechnology, cell biology, biochemistry or equivalent experience (defined as High School Diploma/GED and 4 years progressive experience in a technical field or project management)
An understanding of support processes, customer needs and have product knowledge
Solid technical knowledge of Cytiva Upstream and Downstream equipment
Ability to work effectively across functions to deliver results and execute multiple commitments within the Global Environment
Experience with and understanding of the methods of equipment qualifications in GxP environment
Strong knowledge of relevant industrial standards such as GAMP5, ASTM E2500, ISPE, ICH
Multitasking abilities to drive critical issues simultaneously
Resourcefulness, commitment, interpersonal, communication and negotiation skills
Excellent verbal and written communication skills in English
Excellent skills in MS Office products
Be based in EMEA region with ability to travel within EMEA(60%) and globally (15%) to support customer needs
Experience as Field Engineer within the Cytiva portfolio is a plus

Who we are:
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Selection and interviews will happen continuously and the last application day.

Alla platsannonser →

Andra jobb i Uppsala som Civilingenjör, bioteknik

Nedan visas andra jobb i Uppsala som Civilingenjör, bioteknik.

Scientist Protein Characterization

Läs mer Apr 9
Who we are
Olink Proteomics is a rapidly growing life science company committed to advancing the understanding of human diseases through proteomics. We are dedicated to innovation, quality, rigor, and transparency, providing outstanding solutions and support for human protein biomarker discovery.
The vital role of proteins in understanding human biology has been recognized for many decades, but technological limitations severely restricted the comprehensive investigation of the vast number of proteins that could be important in different biological processes and diseases. With Olink, scientists can now simultaneously measure thousands of human proteins using just a few µL of blood sample, with highly specific, thoroughly validated assays that cover a very wide dynamic range (fg/mL to µg/mL).
In a few years, Olink has grown rapidly from a small, Sweden-based company offering assays for a few hundred proteins, to a NASDAQ-listed organization with a strong global presence, a broad portfolio of flexible protein biomarker solutions and library of high quality, thoroughly validated assays that covers 5400+ proteins.
For more information about Olink, please visit www.olink.com
Position Description
This position is organized in the Protein Characterization team, R&D Department Affinity. The role is centered around LC-MS methods for research and development of Olink affinity reagents in the area of protein characterization and includes hands-on wet-lab work. The role is expected to enhance development, trouble-shoot and benchmark both new and existing protein binders. You will have the opportunity to work on challenging projects, collaborate with cross-functional teams and contribute to the development of new products based on the Olink PEA (Proximity Extension Assays) technology.
Primary Responsibilities
Set up and apply mass spectrometry methods for protein quantification and sequence determination of purified and complex samples beneficial for the sustainability and growth of Olink product lines.
Work independently in the Protein Characterization team with active communication across internal and external interfaces.
Lead and have accountability for ongoing internal or external projects.
Plan, execute, report, and scientifically communicate outcomes of R&D studies within own area.
Interpret internal or external issues related to affinity reagents and recommend solutions, based on data driven insight.
Independently support colleagues in development or research activities.
Work in accordance with Olink’s quality system and relevant instructions for laboratory work.
Comply with company instructions and routines including environmental health and safety.

Qualifications/skills
Ph.D. in a relevant life sciences field (e.g., Analytical Chemistry, Biochemistry, Biotechnology) or equivalent experience.
At least three years industrial or equivalent R&D experience as an independent scientist using LC-MS/MS methods for protein characterization and sequencing.
Knowledge of single and multiplex immunoassay techniques.
Solid theory of mass spectrometry for relative and absolute protein quantitation of proteoforms.
Scientific understanding of the current field of proteomics and bioinformatics.
Data analysis skills using R or Python for scientific validity.
Effective communication and writing skills for presentation and documentation in English.

To enjoy working in the Affinity Department and in R&D you are an open-minded, inclusive, and creative person. You have critical thinking abilities and appreciate paying attention to detail. Finally, you have strong problem-solving skills, using novel approaches and perspectives where needed.
The selection process is on-going, and the position might get filled before the last day of application so please apply as soon as possible, however no later than 2024.04.30.
Please observe that we would like to receive anonymous applications!

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Development Engineer - Focus

Läs mer Feb 2
Who we are

Olink Proteomics is a rapidly growing life science company committed to advancing the understanding of human diseases through proteomics. We are dedicated to innovation, quality, rigor and transparency, providing outstanding solutions and support for human protein biomarker discovery.

The vital role of proteins in understanding human biology has been recognized for many decades, but technological limitations severely restricted the comprehensive investigation of the huge number of proteins that could be important in different biological processes and diseases. With Olink, scientists can now simultaneously measure thousands of human proteins using just a few µL of blood sample, with highly specific, thoroughly validated assays that cover a very wide dynamic range (fg/mL to µg/mL).

In a few years, Olink has grown rapidly from a small, Sweden-based company offering assays for a few hundred proteins, to a NASDAQ-listed (https://eur01.safelinks.protection.outlook.com/?url=https://investors.olink.com/investor-relations&data=05|01|thomas.bennett@olink.com|44d00a4e60cc45da8f8b08da2d189513|0bc012cfb3e946bd95a6cecc37315bb1|1|0|637871880838157918|Unknown|TWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0=|3000|||&sdata;=/1avRLTDgaZQT7/HLQVoC2z6iY/lV6p088C3xz0TkuI=&reserved=0) organization with a strong global presence, a broad portfolio (https://eur01.safelinks.protection.outlook.com/?url=https://www.olink.com/products-services/&data=05|01|thomas.bennett@olink.com|44d00a4e60cc45da8f8b08da2d189513|0bc012cfb3e946bd95a6cecc37315bb1|1|0|637871880838157918|Unknown|TWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0=|3000|||&sdata=67Dhfg2OK3oTJU4HR9ipLduzEFYVrwrcHRERFZ+Shm8=&reserved=0) of flexible protein biomarker solutions and library of high quality, thoroughly validated assays that covers ~5400 proteins.

For more information about Olink, please visit www.olink.com

Position Description

We are seeking a highly motivated and driven Development Engineer to join our R&D team responsible for development of our customized product - Olink Focus. In this role, you will lead your own projects and the work is carried out in close contact with the customer, with high demands on good communication, high quality work, and deliveries within set timeframes. You will have the opportunity to work on new and exciting customer projects and contribute to the development of future innovative products.

Primary Responsibilities

- Project planning and follow-up on set timelines

- Ordering of reagents, planning and executing of laboratory experiments

- Evaluation and analysis of experimental results

- Compiling and reporting of results, internally and externally to customers

- Participation in customer meetings during the development process of the projects

- Take an active part in the team´s continuous improvement work

Qualifications/skills

- University degree in life sciences (e.g., Biochemistry, Molecular Biology, Immunology) or corresponding education

- Minimum of 5 years of experience in development work within the field

- Documented skills and experience in laboratory work (e.g., DNA sequencing techniques such as PCR, qPCR and NGS)

- Experience of project management

- Strong analytical and problem-solving skills

- Excellent teamwork and communication skills

- Flexible, customer oriented and pragmatic

- Familiarity with relevant software and data analysis tools

If you are driven and customer focused with a passion for developing innovative protein assays and want to be part of a team at the forefront of biotechnology, we encourage you to apply. Please submit your resume and a cover letter detailing your relevant experience and why you are the ideal candidate for this position. The last day of application is on the 25th of February.

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Scientist Oligo Design

Läs mer Jan 5
Who we are

Olink Proteomics is a rapidly growing life science company committed to advancing the understanding of human diseases through proteomics. We are dedicated to innovation, quality, rigor and transparency, providing outstanding solutions and support for human protein biomarker discovery.

The vital role of proteins in understanding human biology has been recognized for many decades, but technological limitations severely restricted the comprehensive investigation of the huge number of proteins that could be important in different biological processes and diseases. With Olink, scientists can now simultaneously measure thousands of human proteins using just a few µL of blood sample, with highly specific, thoroughly validated assays that cover a very wide dynamic range (fg/mL to µg/mL).

In a few years, Olink has grown rapidly from a small, Sweden-based company offering assays for a few hundred proteins, to a NASDAQ-listed (https://eur01.safelinks.protection.outlook.com/?url=https://investors.olink.com/investor-relations&data=05|01|thomas.bennett@olink.com|44d00a4e60cc45da8f8b08da2d189513|0bc012cfb3e946bd95a6cecc37315bb1|1|0|637871880838157918|Unknown|TWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0=|3000|||&sdata;=/1avRLTDgaZQT7/HLQVoC2z6iY/lV6p088C3xz0TkuI=&reserved=0) organization with a strong global presence, a broad portfolio (https://eur01.safelinks.protection.outlook.com/?url=https://www.olink.com/products-services/&data=05|01|thomas.bennett@olink.com|44d00a4e60cc45da8f8b08da2d189513|0bc012cfb3e946bd95a6cecc37315bb1|1|0|637871880838157918|Unknown|TWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0=|3000|||&sdata=67Dhfg2OK3oTJU4HR9ipLduzEFYVrwrcHRERFZ+Shm8=&reserved=0) of flexible protein biomarker solutions and library of high quality, thoroughly validated assays that covers ~5400 proteins.

For more information about Olink, please visit www.olink.com

Position Description

Scientist - Technical Projects

Olink Proteomics continues to grow, and we are now seeking a Scientist to join our R&D team with a focus on oligo design and technical development for our highplex products. Technical Projects works with developing technical solutions for new products as well as improving existing products. The work is performed in projects where one or several projects are run in parallel. The role is based in our Uppsala headquarters.

Primary responsibilities

- Design oligos for highplex products.

- Analyze large data sets and draw conclusions.

- Design and evaluate molecular methods.

- Plan and perform laboratory experiments to validate and optimize protocols and technical solutions.

- Documenting results in technical reports.

Qualifications/skills

- Ph.D. from the Life Science area.

- A deep knowledge in molecular biology and nucleic acid structure prediction.

- Documented experience with bioinformatics tools.

- Proficiency in Python and/or Perl.

- Experience of tackling complex analytical workflows.

- Experience from method development especially experience with multiplex assay development is highly desirable.

- Experience from molecular techniques such as NGS, qPCR and PCR.

- Well documented experience from lab work.

- Experience of working in projects.

To succeed in this role, we believe that you are committed, driven and solution oriented. You are a team player that can work with many personalities and you are thorough and have strong problem-solving skills. It is also important that you are positive and can adjust to changed circumstances.

Please submit your resume and a cover letter detailing your relevant experience and why you are the ideal candidate for this position. The last day for applying is on the 28th of January 2024 but please submit your application as soon as possible.

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Development Engineer QC -Design transfer

Läs mer Dec 21
Who we are

Olink Proteomics is a rapidly growing life science company committed to advancing the understanding of human diseases through proteomics. We are dedicated to innovation, quality, rigor and transparency, providing outstanding solutions and support for human protein biomarker discovery.

The vital role of proteins in understanding human biology has been recognized for many decades, but technological limitations severely restricted the comprehensive investigation of the huge number of proteins that could be important in different biological processes and diseases. With Olink, scientists can now simultaneously measure thousands of human proteins using just a few µL of blood sample, with highly specific, thoroughly validated assays that cover a very wide dynamic range (fg/mL to µg/mL).

In a few years, Olink has grown rapidly from a small, Sweden-based company offering assays for a few hundred proteins, to a NASDAQ-listed organization with a strong global presence, a broad portfolio of flexible protein biomarker solutions and library of high quality, thoroughly validated assays that covers ~5300 proteins.

For more information about Olink, please visit?www.olink.com

Position Description

Olink continues to grow, and we are now looking for a Development Engineer Quality Control -Design transfer to join our Quality Control team within Supply Chain. The QC team, which today consists of 10 people, is divided into two sub-teams: One with a focus on checking raw materials, components and finished products and one where the focus is on receiving and implementing new QC methods from RnD/ the Design Transfer process. As the company grows, the need for an additional Development Engineer with a focus on Design transfer activities has increased. The main purpose of the position is to lead the project activities and be responsible for transfer of methods from RnD to Quality Control. The position is based in our Uppsala headquarters and reports to Head of Quality Control.

Primary Responsibilities

- Lead and coordinate projects and activities within Quality Control.

- Actively participate as core team member in Product Development projects (NPI).

- Be responsible for driving the QC preparation tasks in the Design transfer process according to internal procedures and routines and act as the Quality Control Preparation Engineer.

- Write and review instructions and QC methods.

- Manage and drive product care activities within Supply Chain including improvements, non-conformities, CAPAs and Change Control activities.

- Actively participate in the business development of the department, i.e. create and improve work processes and routines.

Qualifications/skills

- MSs within Biotechnology/ Molecular Biology or similar.

- At least 2 years’ experience from a role as development engineer or similar within Life Science.

- Experience from a similar role as PM/Member/ Production Preparation Engineer of various Product Development Projects.

- Experience/ knowledge with ERP systems.

- Experience from ISO13485 certified or IVD/MD regulated business is highly beneficial.

- Fluent in (speaking/reading/writing) both Swedish and English is mandatory and necessary to be successful in this role.

As a person, you should be interested in, and enjoy driving and leading activities and projects. You are a solution oriented team player with integrity who can be pragmatic when needed. You are also open towards changes and is motivated by driving improvements together with others.

The selection process is on-going, and the position might get filled before the last day of application so please apply as soon as possible, however no later than 2024.01.14. We accept applications both in English and Swedish.

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Mekanisk ingenjör till Life Science företag i Uppsala

Läs mer Apr 24
Vi söker nu en mekanisk ingenjör för konsultuppdrag hos vår kund inom Life Science i Uppsala!

Arbetsuppgifter

Arbetsuppgifterna innefattar men begränsas ej till;

• Kvalitetskontroller av mekanikråvaror
• Kalibrera, kontrollera och underhålla instrument
• Utreda och rapportera avvikelser
• Förbättra processer och rutiner i alla steg alla steg av verksamheten

Vem söker vi?

Vi söker dig som har en högskole/universitetsutbildning inom mekanik eller motsvarande. Du har god kommunikationsförmåga i svenska och engelska, samt goda IT-kunskaper. Vi lägger stor vikt vid dina personliga egenskaper och tror att du är en god teamplayer med stor ansvarskänsla och noggrannhet som trivs i ett stort, internationellt företag här du kan fortsätta din personliga utveckling och bidra till verksamhetens satta mål med dina tidigare erfarenheter och kompetenser.

Anställningsform/omfattning/arbetsort
Visstidsanställning / Heltid / Uppsala

Tillträdesdag
Enligt överenskommelse/omgående - t.o.m årsskiftet med chans till förlängning

Information

Intervjuer kommer att hållas löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. Inför intervju kommer utdrag ur verifiera att göras samt inför anställning kommer drogtest att utföras.
Känns tjänsten intressant så inkom snarast med din ansökan!

Forma framtiden med oss!
Lernia utvecklar framtidens arbetskraft. Det gör vi genom att utbilda, matcha, bemanna och rekrytera. Snabbt och utan krångel löser vi arbetsmarknadens behov så att människor och företag kan nå sin fulla potential. Det har varit vår uppgift i över hundra år. Lernia omsatte 3,3 miljarder kronor 2022 och finns över hela landet. Vi utbildade och coachade 19 900 personer och förmedlade 11 500 bemanningskonsulter. 13 700 personer fick möjlighet till nytt jobb genom våra tjänster.
Läs mer på lernia.se.

Ansök nu

Andra jobb i Uppsala från Cytiva Sweden AB

Nedan visas andra jobb i Uppsala från Cytiva Sweden AB .

Lead IT Systems Engineer

IT-arkitekt/Lösningsarkitekt
Läs mer Maj 17
Nytt
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 IT Systems Engineer for Cytiva is responsible for overseeing the development of Operational Technology (OT) systems and networks across six Cytiva locations, with a particular emphasis on supporting the sites in Poland and Sweden. You will be working with cross functional project teams in the development, implementation, and maintenance of Operational Technology (OT) Data Centers. You will be an enabling force to meet the need of internal customers, which includes new product design support/design transfer, manufacturing sites, and other users who need R&D and development infrastructure capabilities.
This position is part of the Automation, Digital, and Learning department located in Uppsala, Sweden and will be hybrid. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
Network Security and Firewall Management: Ensure the network is secured with up-to-date Palo Alto Firewall configurations and security benchmarks. Regularly update the firewall OS and implement threat prevention measures to protect against vulnerabilities and attacks.
Switch Configuration and Maintenance: Maintain and configure Cisco switches according to the latest standards, ensuring that firmware is up-to-date and that the switches are configured for optimal performance and security.
Network Monitoring and Performance: Implement a robust network monitoring system that can track the performance and health of the network, including the switches and firewalls.
Access Control and Authentication: Manage access control lists (ACLs) and implement proper authentication methods to control access to the network and its resources.
Disaster Recovery and Business Continuity: Develop and maintain a comprehensive disaster recovery and business continuity plan that includes the network infrastructure. Ensure that backup management and recovery procedures are in place and tested regularly.

The essential requirements of the job include:
A bachelor's degree in Computer Science, Information Technology, or a related field to provide a strong foundation in networking principles and technologies.
Possession of a Cisco Certified Network Associate (CCNA) certification or equivalent to demonstrate practical skills in managing Cisco switches and understanding network protocols.
At least 3-5 years of experience in network administration or management, with a focus on industrial or research and development environments.
Proficiency in configuring and managing Palo Alto Firewalls, as well as experience with network security, switch configuration, and network performance monitoring.
Strong analytical and problem-solving skills, effective communication abilities, and the capacity to work collaboratively with cross-functional teams.

It would be a plus if you also possess previous experience in:
Advanced Networking Skills: Experience with advanced networking concepts and protocols beyond CCNA, such as CCNP (Cisco Certified Network Professional) or AWS networking, to handle complex network architectures and cloud-based environments.
Cybersecurity Expertise: Knowledge of cybersecurity principles and experience with technical support in cybersecurity, which is crucial for protecting the network against evolving threats.
Project Management and Agile Framework: Skills in project development and execution, which are essential for managing network-related projects, ensuring they are completed on time and within budget.

At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.
At Danaher we bring together science, technology and operational capabilities to 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. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. 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.

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Senior Software Test Engineer

Mjukvaruutvecklare
Läs mer Maj 4
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. Our software products are essential cornerstones for the success of our BioPharma instruments.
We are looking for a Senior Software Test Engineer with DevOps experience to work as Verification Leader for our Software team within Genomic Medicine R&D in Uppsala. The team is in a ramp up phase and will be part of a wider project team that develops a new product for the Nucleic Acid Therapeutics space.
What you'll do:
As a Senior Software Test Engineer with DevOps experience, you will work with requirements and testing process within the software team. You will be part of a scrum team that works in a dynamic environment where you will be involved in the entire development process, from requirements management, implementation and testing to verification.
Together with the team, you will plan and develop new features as well as maintenance of existing code. You will also analyze requirements, develop test plans and test cases. Design and develop test automation framework. Maintain the DevOps development build pipelines and integrate the test automation framework into the build process. Support our customer support team with technical expertise on our products as well as being part of technical investigations of customer issues.
The essential requirements of the job include:
We are looking for someone who has the drive and passion for technology development with multiple years of experience in manual and GUI automation testing of windows application and experience in Azure DevOps pipeline handling.
We are looking for someone who:
Has a university degree in Software Engineering, Computer Science or equivalent experience.
Working experience with software testing.
Working experience as software test leader.
Working knowledge of test management software and Azure DevOps pipeline.
Hands-on experience in developing test automation frameworks.
Experience with C# .NET framework, Windows application.
Experience working with virtual machines.
Communicates fluently in speech and writing in English and preferable also Swedish.

It would be a plus if you also possess previous experience in:
Biotechnology/Life Sciences industry or other regulated environment.
Good Documentation Practices.

At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.
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 Jens Örnberg at jens.ornberg@cytiva.com. We look forward to hearing from you!
At Danaher we bring together science, technology and operational capabilities to 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. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. 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.

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Produktionsingenjör med teamleaderansvar

Produktionsingenjör, kemi
Läs mer Maj 4
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 Produktionsingenjör med Team Leader ansvar till sektionen Kolonnproduktion på vår produktionsanläggning i Uppsala. Vi är idag en grupp på 14 operatörer 3 ingenjörer och en sektionschef som tillsammans arbetar för att tillverka kromatografikolonner till Cytivas kunder runt om i världen.
Vad du ska göra:
Delta i processvårdsprojekt samt driva upp- och nedskalning och flytt av processer och produktionsutrustning.
Driva och delta i förbättringsarbete och problemlösning inom processansvarsområdet.
Följa produktionsutfall, uppmärksamma kvalitetsbrister och rapportera dessa i kvalitetssystem samt initiera och driva åtgärder för dessa inom ramen för processansvar.
Stötta samordnade operatörer i gruppen som ansvarar för den dagliga planeringen av produktionen och stötta med veckoplanering och bevilja kortare ledigheter.
Koordiera det dagliga arbetet genom Daily Management för att säkerställa leveransmålen.
Introducera ny personal.
Driva grundorsaksanalyser och riskbedömningar
Tillsammans med sektionschef utveckla teamets arbetssätt och implementera förbättringar genom DBS-verktyg.

De huvudsakliga kraven för tjänsten är:
Civilingenjör eller motsvarande med inriktning mot bioteknik/kemiteknik/maskinteknik eller liknande utbildningsbakgrund.
Du behärskar svenska och engelska flytande i tal och skrift.
God datorvana och trygg användare av olika IT-system.

Det är även meriterande om du har tidigare erfarenhet av:
Erfarenhet av att leda och fördela arbete.
Kunskap om leanmetodik.
Tidigare erfarenhet av kolonnpackning.

För att vara framgångsrik i rollen som produktionsingenjör med teamleaderansvar ser vi gärna att du som söker är en säkerhets- och kvalitetsmedveten person med god förmåga att ta initiativ och driva flera parallella aktiviteter samtidigt. Rollen ställer krav på din förmåga att leda och koordinera olika arbetsaktiviteter och det är därför viktigt att du är en god kommunikatör med sinne för struktur, planering och prioritering.
Urval och intervjuer sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. För frågor rörande den här tjänsten vänligen kontakta rekryterande chef Martina Brolin martina.brolin@cytiva.com. Varmt välkommen med din ansökan!

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Software Engineer

Mjukvaruutvecklare
Läs mer Maj 4
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. Our software products are essential cornerstones for the success of our BioPharma instruments.
We are looking for a Software Engineer to work with our Software team within Genomic Medicine R&D in Uppsala. The team is in a ramp up phase and will be part of a wider project team that develops a new product for the Nucleic Acid Therapeutics space.
What you'll do:
In the role as Software Engineer at Cytiva, you will work together with your team in a dynamic and agile environment. You will bring valuable software expertise to the team and work closely with colleagues from other areas such as Technical Writers, UX and Application Specialists, Hardware Developers and Product Managers.
You will be involved in the entire development process, from requirements management, implementation and testing to verification and strive to automate more levels of testing.
Tasks include:
Analyzing, designing, and developing new features in our products.
Development and configuration of UNICORN™ for control and monitoring of instruments, including user interface in HTML5/JavaScript, instruction definitions and monitoring parameters.
DevOps tools like Azure DevOps.

The essential requirements of the job include:
We are looking for someone who has the drive and passion for technology development with at least a few years of experience. To be successful in this role, we believe that you are engaged by new challenges, curious about new technology, confident in your skills and enjoy working together to achieve results.
We are looking for someone who:
Has a university degree in Software Engineering, Computer Science or equivalent experience.
Working experience in developing Windows application using some high-level program language, preferable C#.NET.
Communicates fluently in speech and writing in English and preferable Swedish.

It would be a plus if you also possess previous experience in:
Biotechnology/Life Sciences industry or similar regulated environment.
Good Documentation Practices.

At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.
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 Jens Örnberg at jens.ornberg@cytiva.com. We look forward to hearing from you!
At Danaher we bring together science, technology and operational capabilities to 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. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. 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.

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Planner

Planeringsingenjör, kemiteknik
Läs mer Maj 4
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. Your health and wellbeing are important to us and together we will not compromise on safety in the workplace or the environment.
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 Planner to work within our PMO team in the Customized Bioprocess Solutions (CBS) organization at Cytiva's site in Uppsala.
What you’ll do:
As Planner at CBS, you will play a crucial role in overseeing and coordinating various resource assignments for custom and development projects. In this role, you will work closely with project managers, line managers and stakeholders to ensure the successful assignment of resources to ongoing projects. Additionally, you will be leading the continuous work with PMO process improvements and smaller project manager tasks.
The essential requirements of the job include:
Bachelor's Degree and a few years of work experience in manufacturing, logistics, or supply chain management.
Experience working with resource planning.
Knowledge of resource planning systems and tools (Smartsheet, MS Project, etc.).
Ability to communicate on various organizational levels using both Swedish and English language.
Experienced user of Microsoft Office, i.e. Excel, Power Point, and Word.

It would be a plus if you also possess previous experience in:
Knowledge of lean methodologies.
Experience working with custom product development within the biotechnology industry.

To be successful in this role, we believe that you possess strong analytical and problem-solving skills, with the ability to prioritize and make data-driven decisions. Moreover, we believe that you are a well-organized and team-oriented individual with attention to detail and a demonstrated ability to manage multiple tasks and prioritize deadlines.
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 George Glosemeyer at george.glosemeyer@cytiva.com. We look forward to hearing from you!
At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.
At Danaher we bring together science, technology and operational capabilities to 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. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. 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.

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Validation and Verification Engineer

Systemtestare/Funktionstestare
Läs mer Maj 12
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're looking for our next Validation and Verification Engineer to join our Verification and Streaming team within the Customized Bioprocess Solutions (CBS) organization at Cytiva's site in Uppsala. As a Validation and Verification Engineer at Cytiva, you will be responsible for the planning and execution of functional tests of our custom hardware products. This position is located in Uppsala, Sweden and will be an onsite role.
What you'll do:
Plan and execute functional tests of custom hardware products.
Review and reject/approve test results and peer-review of test documentation.
Develop and write procedures for functional testing, perform troubleshooting and suggest corrective actions.
Educate suppliers, customers and service engineers as well as participate in technical discussions with customers during FATs.

The essential requirements of the job include:
BSc degree or equivalent. Alternatively, you have a comparable level of work life experience.
Experience working with hands-on troubleshooting of hardware/machinery.
Fluency in English, both written and spoken.

It would be a plus if you also possess previous experience in:
Knowledge of Cytiva BioProcess products.
Strong technical competence and deep understanding of control software.
Experience from testing/verification of operating systems.
Experience from GMP and/or other regulated business areas or industries.
Fluency in Swedish, both written and spoken.

To be successful in this role, we believe that you are a structured and analytical person with excellent team-working skills. In addition, we believe that you are highly motivated and results-oriented self-starter.
Interview and selection will happen continuously and the opening can be filled before last day of application, May 31st. For questions regarding the role please contact hiring manager Robert Gardelius, robert.gardelius@cytiva.com.
At Danaher we bring together science, technology and operational capabilities to 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. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. 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.

Ansök nu