Process Engineer III

NovartisDurham, CA
$98,700 - $183,300Onsite

About The Position

Step into a pivotal engineering role where your expertise directly shapes advanced manufacturing operations. As a Process Engineer III, you will support the design, validation, maintenance, and lifecycle management of manufacturing equipment, facilities, and utilities. This role requires hands-on experience with automated and manual visual inspection systems and drug product/fill-finish equipment to ensure compliant, reliable, and efficient GMP operations.

Requirements

  • Bachelor’s degree in Chemical, Electrical, or Mechanical Engineering or related technical field
  • Minimum 5 years pharmaceutical or biopharmaceutical GMP manufacturing experience, or equivalent experience
  • Strong knowledge of FDA regulations and GMP systems
  • Demonstrated experience supporting engineering activities in a regulated pharmaceutical or biotechnology environment
  • Experience with automated and manual visual inspection equipment, as well as general drug product / fill-finish production equipment
  • Proven ability to lead cross-functional teams in a fast-paced and dynamic setting
  • Strong project management skills with experience in both strategic and long-term planning
  • Excellent written and verbal communication skills with strong technical writing capabilities
  • Ability to analyze complex issues and implement effective, compliant engineering solutions

Nice To Haves

  • Business Continuity
  • Change Control
  • Cost Management
  • Data Analytics and Digital
  • Engineering Technical Expertise
  • GDP Knowledge
  • gmp knowledge
  • HSE Knowledge
  • Knowledge Of Relevant Tools And Systems
  • Manufacturing Process (Production)
  • Operational Excellence
  • Quality Compliance
  • Resilience and Risk Management
  • Total Productive Maintenance

Responsibilities

  • Support the design, validation, maintenance, and lifecycle management of manufacturing equipment, facilities, and utilities.
  • Ensure compliant, reliable, and efficient GMP operations.
  • Utilize hands-on experience with automated and manual visual inspection systems and drug product/fill-finish equipment.

Benefits

  • performance-based cash incentive
  • annual equity awards
  • health, life and disability benefits
  • 401(k) with company contribution and match
  • vacation
  • personal days
  • holidays
  • other leaves
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