Process Engineer Iii

Novartis UK

Durham, United Kingdom
Base: $98,700 - $183,300; bonus/equity: performanc...
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Equipment life cycle management
Process deviation investigation
Fda and internal audit participation
** Novartis UK is seeking a Process Engineer III in Durham, responsible for engineering, validation, and maintenance support for process manufacturing equipment in a new large molecule drug substance facility. The ideal candidate should possess a B.S. degree in engineering and have significant experience in GMP manufacturing operations, with a focus on team collaboration and project management skills. **

Job Summary

  • The Process Engineer III is responsible for providing engineering, validation and maintenance support to the process manufacturing equipment, facility and utilities at a site.
  • The initial responsibilities for this role will be to support the design, build, and qualification of the equipment for a new large molecule drug substance facility.
  • US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits.

Matching Summary

Match Score: 75

** Novartis UK is seeking a Process Engineer III in Durham, responsible for engineering, validation, and maintenance support for process manufacturing equipment in a new large molecule drug substance facility. The ideal candidate should possess a B.S. degree in engineering and have significant experience in GMP manufacturing operations, with a focus on team collaboration and project management skills. **

Salary

Base: $98,700 - $183,300; Bonus/Equity: performance-based cash incentive and eligibility for annual equity awards; Benefits: comprehensive benefits package including health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits

Skills & Requirements

Must-have

  • Equipment life cycle management
  • Process deviation investigation
  • FDA and internal audit participation
  • Equipment reliability strategies
  • User Requirements (URS) development
  • Facility and equipment strategic planning

Nice-to-have

  • Mentorship of other engineers
  • Leading internal teams
  • Evaluation of new technologies

Key Requirements

  • B.S. degree in Chemical, Electrical or Mechanical Engineering, or related technical field, with 5 years work experience in pharmaceutical or biopharmaceutical based GMP manufacturing operations, or equivalent work experience (9 years)
  • In-depth knowledge of FDA regulations and GMP systems
  • Strong project management skill set
  • Ability to lead cross functional teams

Work Rights

Not specified

Tailored Resume

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