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Quality Assurance Specialist

vor 3 Monaten


Cologne, Deutschland Cytiva Vollzeit

Be part of something altogetherlife-changing

Workingat Cytiva means being at the forefront of providing new solutionsto transform human health. Our incredible customers undertakelife-saving activities ranging from fundamental biological researchto developing innovative vaccines, new medicines, and cell and genetherapies.

At Cytiva you willbe able to continuously improve yourself and us – working onchallenges 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 learningopportunity – so you can grow your career and expand your skills inthe long term.

Forming part ofthe Biotechnology segment at Danaher, we bring together dedicatedtechnical expertise and talent to develop the next generation oflife-changingtherapeutics.

TheQuality Assurance Specialist (m/f/d) for Cytivais responsible to support QA operations in the viral vector cellline development business.


Thisposition is part of the Viral Vector business unit in the GenomicMedicine Operation Company located in Cologne, will be hybrid andtemporary for 24 months. At Cytiva, our vision is, to advancefuture therapeutics from discovery todelivery.

Whatyou willdo:

  • Creation,review and training of SOPs and other quality related documents orprocedures

  • Administration ofe.g., documents in the electronic DMS system and support theadministration and maintenance of our laboratory monitoringsystem

  • Change control anddeviation management, follow up on required corrective andpreventive actions, monitoring of correspondingmeasures

  • Monitoring andapproval of internal and external cell banktests

  • Support the teams incontinuous improvement of internal processes using tools asKaizen

Whoyouare:

  • Degreein Biology, Biotechnology or comparablequalification

  • Demonstratedexperience to understand Quality requirements related to ISO9001

  • Computer literate(Word, Excel, Electronic DocumentationSystem)

  • Proven experience ina global workingenvironment

  • Fluent inwritten and spokenEnglish


It would be a plus if you also possess previousexperiencein:

  • PreferablyQuality Management experience according to e.g. ISO 9001 or ISO13485

  • Ideally even goodknowledge in current GMPregulations

  • Knowledge oflaboratory or cell culturework 

Benefits

  • Attractivesalary

  • Developmentopportunities at Cytiva and within the DanaherGroup

  • Internationalcorporate environment in a rapidly growingindustry

AtDanaher we bring together science, technology and operationalcapabilities to accelerate the real-life impact of tomorrow’sscience and technology. We partner with customers across the globeto help them solve their most complex challenges, architectingsolutions that bring the power of science to life. Our global teamsare pioneering what’s next across Life Sciences, Diagnostics,Biotechnology and beyond. For more information, visit

AtDanaher, we value diversity and the existence of similarities anddifferences, both visible and not, found in our workforce,workplace and throughout the markets we serve. Our associates,customers and shareholders contribute unique and differentperspectives as a result of these diverseattributes.