Process Engineering Lead, Automated Visual Inspection (holly Springs)

Genentech

Holly Springs, NC, US
Base: $95,200 - $176,800 for principyl engineer, $...
Fully remote
Automated visual inspection expertise
Project management for technology implementation
Machine vision system engineering
Genentech is launching a state-of-the-art manufacturing facility in Holly Springs focused on next-generation technology and operational excellence for drug product manufacturing

Job Summary

  • Genentech is launching a state-of-the-art manufacturing facility in Holly Springs focused on next-generation technology and operational excellence for drug product manufacturing.
  • The Process Engineering Lead will oversee the green-field Automated Visual Inspection program from design through startup and ongoing operations, ensuring regulatory compliance and high-quality defect detection.
  • The role offers relocation benefits, discretionary annual bonus, and requires collaboration with global teams, technology suppliers, and regulatory agencies in a fast-paced, entrepreneurial environment.

Matching Summary

Genentech is launching a state-of-the-art manufacturing facility in Holly Springs focused on next-generation technology and operational excellence for drug product manufacturing.

Salary

Base: $95,200 - $176,800 for principal engineer, $114,300 - $212,420 for distinguished engineer; Bonus/Equity: Discretionary annual bonus available; Benefits: Relocation benefits provided

Skills & Requirements

Must-have

  • Automated Visual Inspection expertise
  • Project management for technology implementation
  • Machine vision system engineering
  • Process validation and qualification
  • Regulatory compliance with health authorities
  • Operator and technician training and mentoring
  • Continuous improvement and optimization

Nice-to-have

  • Data science and analytics skills
  • Smart factory technology knowledge
  • Advanced interpersonal and coaching skills
  • Experience with technology transfers
  • Strong organizational skills
  • Ability to work in global environment
  • Safety culture advocacy

Key Requirements

  • Bachelor’s, Master’s, or Ph.D. in bio/chemical engineering or similar
  • 11+ years pharmaceutical industry experience
  • 5+ years Automated Visual Inspection experience
  • Experience with regulatory submissions and inspections
  • Up-to-date knowledge of cGMP and Health Authority regulations
  • Ability to travel up to 20%
  • Experience in parenteral drug manufacturing

Work Rights

Not specified

Tailored Resume

Cover Letter