Product Engineer 23 months FTC

Radiometer; Cardiff; Vor Ort; GBP 42.000 - 64.000; Vollzeit

Zusammenfassung

Cytiva, part of Danaher, seeks a Mechanical/Manufacturing Engineer to support Lab Filtration product lifecycle in Cardiff on a 23-month fixed-term contract. You will drive design changes, document control, and quality activities across Operations, Quality, Supply Chain and Process Engineering.

You will apply structured problem-solving, interpret drawings (SolidWorks), and contribute to NPD, product transfers, risk assessments, and validations while identifying improvements in manufacturability,

Qualifikationen

• Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Product Design, Materials Engineering, Biomedical Engineering, or related technical discipline.
• Experience in product engineering, sustaining engineering, product development, manufacturing engineering, or quality engineering within a manufacturing environment.
• Experience interpreting engineering drawings (SolidWorks) and product specifications and supporting controlled changes to products, materials, components, processes, or technical records.
• Experience applying structured problem-solving and root-cause analysis methods to technical or manufacturing issues.
• Experience working within a quality management system and collaborating with cross-functional stakeholders to complete documented engineering deliverables.
• Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel – 10% travel, overnight, within territory or locations; must have a valid driver’s license with an acceptable driving record.
• It would be a plus if you also possess experience in life sciences, filtration, medical devices, diagnostics, biotechnology, or another regulated industry; experience supporting design verification, validation, risk management, product qualification, or supplier-change activities; experience using PLM or electronic quality/document-management systems.

Aufgaben

• Support product lifecycle activities for Lab Filtration products, including design changes, product improvements, technical documentation, specifications, bills of materials, obsolescence, and product rationalisation.
• Investigate product and manufacturing issues affecting safety, quality, delivery, or cost; apply structured problem-solving methods and work with Operations, Quality, Supply Chain, and Process Engineering to implement corrective actions.
• Contribute engineering deliverables to new product development, product transfer, supplier change, verification, validation, risk assessment, design review, and product qualification activities.
• Prepare and maintain accurate engineering and quality records in accordance with Cytiva procedures and applicable requirements, including support for non-conformance, CAPA, complaint, deviation, audit, and inspection activities.
• Identify and deliver continuous-improvement and productivity opportunities that improve product performance, manufacturability, quality, cost, or operational reliability.

Kenntnisse

Structured problem-solving

Root cause analysis

Cross-functional collaboration

Manufacturing engineering

Quality mindset

Ausbildung

Bachelor's degree in Mechanical/Manufacturing Engineering or related

Tools

SolidWorks

PLM systems

Document control systems

Jobbeschreibung

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 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. This role is offered on a 23 month Fixed Term Contract with the potential to be extended/ made permanent in the future Learn about the Danaher Business System which makes everything possible.

What you will do:

Support product lifecycle activities for assigned Lab Filtration products, including design changes, product improvements, technical documentation, specifications, bills of materials, obsolescence, and product rationalisation. Investigate product and manufacturing issues affecting safety, quality, delivery, or cost; apply structured problem‑solving methods and work with Operations, Quality, Supply Chain, and Process Engineering to implement corrective actions. Contribute engineering deliverables to new product development, product transfer, supplier change, verification, validation, risk assessment, design review, and product qualification activities. Prepare and maintain accurate engineering and quality records in accordance with Cytiva procedures and applicable requirements, including support for non conformance, CAPA, complaint, deviation, audit, and inspection activities. Identify and deliver continuous‑improvement and productivity opportunities that improve product performance, manufacturability, quality, cost, or operational reliability.

Who you are:

• Bachelor's degree, or equivalent recognised qualification, in Mechanical Engineering, Manufacturing Engineering, Product Design, Materials Engineering, Biomedical Engineering, or a related technical discipline.
• Practical experience in product engineering, sustaining engineering, product development, manufacturing engineering, or quality engineering within a manufacturing environment.
• Experience interpreting engineering drawings (SolidWorks experience) and product specifications and supporting controlled changes to products, materials, components, processes, or technical records.
• Experience applying structured problem‑solving and root‑cause analysis methods to technical or manufacturing issues.
• Experience working within a quality management system and collaborating with cross-functional stakeholders to complete documented engineering deliverables.
• Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel – 10% travel, overnight, within territory or locations Must have a valid driver’s license with an acceptable driving record
• It would be a plus if you also possess previous experience in:
  • Experience in life sciences, filtration, medical devices, diagnostics, biotechnology, or another regulated industry.
  • Experience supporting design verification, validation, risk management, product qualification, or supplier-change activities.
  • Experience using product lifecycle management, or electronic quality/document-management systems.

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. Danaher is a leading global life sciences, biotechnology, and diagnostics innovator, helping to solve many of the world’s most important health challenges, ultimately improving quality of life for billions of people today, while setting the foundation for a healthier, more sustainable tomorrow. The Danaher ecosystem is made up of more than 15 businesses united by a shared commitment to innovate for tangible impact. Please read our Applicant Data Privacy Notice carefully here.