Senior CQV Engineer - GMP Validation Leader

Lonza

Bend (OR)

Vor Ort

Vertraulich

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Day-one medical, dental, vision, life,
401(k) with company match up to 6%
Disability insurance
Exposure to advanced biomanufacturing

Zusammenfassung

Lonza in Bend, Oregon seeks a Senior CQV Engineer to lead engineering activities supporting research, operations, facilities, and capital projects. The role requires troubleshooting, design, commissioning, qualification of manufacturing equipment and processes, and preparation of engineering docs and SOPs.

You will support change controls, validation, GMP compliance, and partner with cross-functional teams to assess risks and improve reliability and performance, enabling safe and efficient

Qualifikationen

  • Bachelor's degree in Engineering or equivalent.
  • 5+ years of engineering experience in regulated manufacturing.
  • Knowledge of GMP and validation principles.

Aufgaben

  • Lead engineering activities supporting research, operations, facilities, and capital projects.
  • Troubleshoot equipment and systems while driving continuous improvements.
  • Design, improve, commission, and qualify manufacturing equipment and processes.
  • Prepare and review engineering documentation, protocols, reports, and SOPs.
  • Support change controls, validation activities, and GMP compliance.
  • Partner with cross-functional teams to assess risks and improve system reliability and performance.
  • Support manufacturing operations to ensure safe, reliable production.

Kenntnisse

Strong technical
Analytical
Problem solving
Cross-functional collaboration

Ausbildung

Bachelor's degree in Engineering

Jobbeschreibung

Lonza in Bend, Oregon seeks a Senior CQV Engineer to lead engineering activities supporting research, operations, facilities, and capital projects. The role requires troubleshooting, design, commissioning, qualification of manufacturing equipment and processes, and preparation of engineering docs and SOPs.

You will support change controls, validation, GMP compliance, and partner with cross-functional teams to assess risks and improve reliability and performance, enabling safe and efficient

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