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.

Your responsibilities will include:

• Oversee microbiological and contamination control processes in cleanroom manufacturing, including environmental monitoring, product release testing, method development, and other laboratory tasks in the microbiology laboratory.

• Provide technical support to the manufacturing site concerning contamination control processes, including the design and validation of cleanrooms, as well as manufacturing and hygiene procedures.

• Ensure the completion of sterility assurance activities necessary to maintain compliance and support project activities as required.

• Apply quality risk management principles to assess and maintain the contamination control and sterility assurance of products and processes.

• Draft policies, procedures, and work instructions as needed.

Who You Are:

• A BSc in Microbiology or a related field is required.

• A minimum of 3 years of microbiology experience, preferably in the pharmaceutical, medical devices, or biotechnology industry.

• A motivated individual with a strong desire to learn and develop expertise in contamination control and sterility assurance.

• Familiarity with relevant cleanroom and sterilization standards, such as EN ISO 14644, BS EN 17414, EN ISO 11737, and EN ISO 11135.

#LI-Hybrid

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.