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9 дней назад

Senior Process Engineering - Orthopaedics

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
UK
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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TL;DR
Senior Process Engineering - Orthopaedics (Medical Devices): Owning and optimizing manufacturing value streams for safe, compliant, and cost-effective orthopaedic medical-device production with an accent on process development, validation, and continuous improvement. Focus on leading IQ/OQ/PQ validation, resolving quality-system actions through root cause analysis, and shaping long-term process and equipment strategy.

Location: Blackpool, Lancashire, United Kingdom; fully onsite

Company

Johnson & Johnson MedTech develops healthcare and medical-device solutions, with the Orthopaedics business planned to become the standalone DePuy Synthes company.

What you will do

  • Own and optimize assigned manufacturing value streams for safe, compliant, cost-effective medical-device production.
  • Provide strategic technical leadership for process development and validation programs.
  • Lead continuous-improvement initiatives across Operations, Quality, R&D, suppliers, and other functions.
  • Manage audit actions, nonconformances, CAPAs, change controls, specifications, and validation protocols.
  • Represent Engineering in governance and regulatory forums while improving quality, supply continuity, and cost performance.
  • Mentor junior engineers and influence long-term process and equipment strategy.

Requirements

  • Bachelor’s degree or equivalent experience in Engineering.
  • Demonstrated manufacturing or process engineering experience.
  • Experience leading equipment, process, and systems validation activities, including IQ, OQ, and PQ.
  • Experience managing audit actions, NCRs, and CAPAs within a Quality Management System.
  • Strong structured problem-solving, root-cause analysis, technical writing, and cross-functional leadership skills.
  • Commitment to HSE practices, regulatory compliance, continuous improvement, and lean manufacturing.

Nice to have

  • Experience with computerized equipment, process control, Gemba Kaizen, lean supply chain management, supply planning, and validation testing.
  • Background in pharmaceutical process engineering or medical-device process improvement.

Culture & Benefits

  • Inclusive work environment focused on respecting individual diversity and dignity.
  • Opportunity to contribute to healthcare innovation and less invasive treatment solutions.
  • Employment may transition to DePuy Synthes following the planned Orthopaedics business separation, subject to legal, regulatory, and consultation requirements.

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