9 дней назад
Senior Product Engineer 23 months FTC (Life Sciences)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Product Engineer 23 months FTC (Life Sciences): Leading technical ownership of Lab Filtration product families, design changes, product transfers, validation, and lifecycle engineering with an accent on regulated manufacturing, product performance, and technical risk management. Focus on resolving complex product and manufacturing issues, driving corrective actions, and improving quality, cost, capacity, reliability, and manufacturability.
Location: Cardiff, United Kingdom. Full-time role with 10% overnight travel within the assigned territory or locations.
Company
operates Cytiva, a life-sciences business developing solutions for biological research, vaccines, medicines, and cell and gene therapies.
What you will do
- Own the technical direction of assigned Lab Filtration product families across performance, design, manufacturing capability, compliance, and lifecycle decisions.
- Lead complex design changes, supplier changes, product transfers, sustaining programmes, and technical workstreams.
- Direct verification, validation, product characterisation, qualification, design review, and technical risk-management activities.
- Resolve significant product, manufacturing, quality, and customer issues through advanced root-cause analysis and corrective and preventive actions.
- Improve quality, cost, capacity, reliability, manufacturability, and customer outcomes while mentoring colleagues and influencing engineering standards.
Requirements
- Bachelor’s degree or equivalent recognised qualification in Mechanical Engineering, Manufacturing Engineering, Product Design, Materials Engineering, Biomedical Engineering, or a related technical discipline.
- Substantial experience in product engineering, sustaining engineering, product development, or regulated manufacturing, including ownership of complex technical deliverables.
- Experience leading multidisciplinary projects or engineering workstreams involving design change, product transfer, supplier change, validation, or product lifecycle management.
- Knowledge of design control, verification and validation, technical risk management, engineering change control, and structured root-cause analysis.
- Ability to influence cross-functional decisions and communicate technical recommendations to Engineering, Quality, Operations, Supply Chain, Product Management, and other stakeholders.
- Valid driver’s license with an acceptable driving record and ability to travel approximately 10%.
Nice to have
- Experience in filtration, life sciences, medical devices, diagnostics, biotechnology, or another regulated industry.
- Experience with supplier qualification, global manufacturing transfer, or business-continuity engineering.
- Working knowledge of quality and regulatory frameworks for healthcare, life-science, or medical-device products.
Culture & Benefits
- 23-month fixed-term contract with potential for extension or transition to a permanent role.
- Continuous-improvement environment based on the Business System.
- Work focused on solutions that support biological research, vaccines, medicines, and cell and gene therapies.
- Collaboration across engineering, quality, operations, supply chain, product management, and related teams.
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