Senior Manufacturing Engineer

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's (https://danaher.com/our-businesses) 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Working at Cytiva 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. Take your next step to an altogether life-changing career. Learn about the Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Manufacturing Engineer is responsible for supporting day-to-day operations including production associates, equipment, and processes to ensure we provide the highest quality products to our customers. The Manufacturing Engineer also provides technical and project leadership to develop and deploy equipment and process upgrades for new product development, cost reduction and quality improvement. This position reports to the Tech Transfer Team Leader and is part of the Operations & Supply Chain team located in Stevenage and will be an on-site role. What you will do:

• Identify, participate in and lead projects that deliver improvements in safety, quality, delivery and cost
• Problem solve process issues and/or product non-conformances using empirical evidence and quantitative analysis
• Participate in New Product Development projects and support the transfer of new products from development into production
• Create process and validation documentation to ensure manufacturing is performed safely and meets the documented quality specifications
• Maintain full regulatory compliance with EHS, quality and legal requirements
  
  Bachelor's degree in Mechanical, Manufacturing or Process Engineering (or a related field) with more than 5 years of relevant experience
• Experience of applying lean manufacturing tools including Daily Management, Standard Work and Lean Conversion
• Equipment and process design and improvement in a regulated industry
• Excellent communicator (written & verbal), comfortable interacting at all levels of the organisation
• Able to work independently and collaborate well across diverse functions in a matrix organisation
Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role
• Able to travel within UK/Europe in support of the role objectives (estimated at 10%)
• Must have a valid driver's license with an acceptable driving record
It would be a plus if you also possess previous experience in:
• Clean room environments in the Pharmaceutical or Medical Device industry
• Formal training, qualification and proven experience in Six Sigma techniques
  
  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.