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.

This position is part of the Quality assurance department located in Newquay and will be a full time on-site roll. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

What you will do:

• Problem solving including NC investigations and root cause.
• Complaint investigations
• Manufacturing line quality support
• Coordination and reporting of relevant failure investigations and subsequent corrective and preventive actions and reviewing effectiveness of these.
• Manage complaint investigations identifying improvement opportunities
• Lead Complaint reduction projects to completion
• Support Cost reduction programmes and lead projects where appropriate
• Support and Lead the operations teams and Engineers when required in the evaluation, trending and reporting of internal and external non-conformances to establish priorities and identify common threads aimed at a continuous reduction in internal non-conformance occurrences via internal or supplier process improvements
• Work with the Engineers to collect, analyse, trend and report data on rejects from routine production inspection and QC tests and related processes to establish improvement priorities and identify common threads aimed at a reduction in external complaints. Work with QA Specialists and others as appropriate to ensure that production inspections and QC tests are aligned with customer needs.
• Ensure required processes, practices and standards in production, quality control and related areas are validated, and continuously improved working with unit managers, manufacturing engineers and team leaders to achieve this.

Who you are:

• Essential Qualifications/Education:

• Degree in Engineering Science or Math's or equivalent quality accreditation/qualification

• Experience in cGMP or ISO quality system manufacturing environment.

• Knowledge in Regulatory, Compliance Systems and Standards

• Supervisory experience

• Experience with Root Cause Analysis Tools, Lean Manufacturing, DBS and or Six Sigma

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.

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.