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 one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.

What You’ll Do:

Manage assigned projects, collect requirements and create requirement documents, test new functionality in a software application.

Work closely with the Engineering, PLM, IT and regulatory teams to pull together requirements and to challenge needs.

Adhere to current QMS and change control processes, but leverage engineering judgement and creativity to continuously improve the processes and improve the quality of product we deliver to customers.

Work closely with other teams often acting as the facilitator for multi arm projects.

Prepare and deliver presentations to customers.

Prepare weekly and monthly project progress reports for the business.

Who Are You:

Bachelor's degree in bioprocessing, mechanical, Instrument or IT engineering

Minimum of 7 years’ experience in the life science industry.

Minimum of 3 years’ experience in managing projects as a project manager or project engineer.

Comfortable working across departments in a hybrid environment.

Comfortable reading and interpreting professional documents and technical procedures.

Experienced writing user requirements specifications or project briefs.

Awareness of GMP and governmental regulations related to drug manufacturing sufficient to appreciate the need for documentation accuracy.

Not afraid to expedite documentation or actions by others supporting the projects.

Nice To Have:

Working knowledge of single use components used in the biotechnology industry and manufacturing processes.

Knowledge of bio-compatible material selection for sterile single-use application in bioprocessing and/or medical device applications.

Knowledge of sterilization methods for pharmaceutical equipment and/or medical devices.

Knowledge of regulatory requirements used in the single use biotechnology industry. 

Formal project management qualification or training

Experience working with software developers.

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.