Process Engineer, Cardiff

Process Engineer

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This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

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.

Summary of purpose of role.

Responsible for developing, implementing, and optimizing production processes to ensure efficient, safe, and cost-effective operations. Minimize equipment downtime and enhance productivity by leading continuous improvement initiatives driven by performance data and root cause analysis.

Work with maintenance and production associates to resolve manufacturing and quality problems related to methods, processes, tooling, equipment, and product design.
Use root cause analysis to solve complex manufacturing and quality issues
Develop manufacturing and/or testing processes with focus on safety, quality, and repeatability for New Product Introduction/Sustainment projects.
Follow best practices around Process Development (PD), Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) with a goal to develop Safe and Quality Processes
Create standard operating procedures (SOP) or work instructions and provide training and guidance to others
Monitor and analyse equipment performance, driving continuous improvement projects.

Position Competencies:

Hold formal qualifications (Bachelors Degree) in an Engineering discipline or time served in a Process/Manufacturing role.
Strong Process Engineering background and a detailed understanding of process validation requirements in a manufacturing environment.
Works well under time-bound pressure as part of a team, and independently.
Strong documentation skills (work instructions, manufacturing plans etc) with a keen eye for detail
Self-motivated and committed to upholding high standards of Safety, Quality and Delivery.
Ability to communicate effectively across all departments and functions.

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.

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Location:: Cardiff
Job Type:: FullTime
Category:: Medical Device

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