As a Principal Process Engineer at Ferring, you will be responsible for driving reliability strategy, failure elimination, and lifecycle optimization for equipment used in sterile pharmaceutical manufacturing. The role involves leading cross-functional investigations, developing dashboards for reliability performance, and ensuring compliance with GMP, sterility assurance, and regulatory requirements.
Requirements
- Bachelor's degree in mechanical, electrical, industrial, or reliability engineering
- Master's degree in Engineering or Reliability Engineering (preferred)
- 8+ years of engineering experience in pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments
- 5+ years in reliability, maintenance, or asset engineering roles
- Direct experience with aseptic or sterile pharmaceutical manufacturing equipment strongly preferred
- Experience with clean utilities (WFI, clean steam, compressed gases) and classified HVAC systems
- Demonstrated experience leading cross-functional technical investigations
Benefits
- Comprehensive healthcare (medical, dental, and vision) with a premium differential
- 401k plan and company match
- Short and long-term disability coverage
- Basic life insurance
- Wellness benefits
- Reimbursement for certain tuition expenses
- Sick time of 1 hour per 30 hours worked
- Vacation time for full time employees
- 15 paid holidays per year
- Paid parental leave subject to a minimum period of employment at Ferring