Senior Process / Project Engineer-2

29

Wilson, NJ, USA
Base: $117,000.00 - $184,200.00; bonus/equity: ann...
**
5 years relevant industrial experience
Gmp pharmaceutical environment experience
Equipment qualification and process validation
** The Senior Process/Project Engineer at Merck in Wilson, NJ, is responsible for technical support related to manufacturing, specifically for packaging and medical device assembly lines. The role involves project management, equipment installation, troubleshooting, and ensuring compliance with quality and regulatory standards, requiring a solid technical background and excellent communication skills. **

Job Summary

  • The Senior Process/Project Engineer provides technical support for the Manufacturing Division-Wilson packaging and medical device assembly lines, including equipment installation and qualification.
  • This role requires leading root cause analysis investigations for equipment-related quality events and providing scientific justification for proposed process changes.
  • Candidates must have a Bachelor's degree in engineering and minimum 5 years of experience working in a GMP Pharmaceutical Environment.

Matching Summary

Match Score: 75

** The Senior Process/Project Engineer at Merck in Wilson, NJ, is responsible for technical support related to manufacturing, specifically for packaging and medical device assembly lines. The role involves project management, equipment installation, troubleshooting, and ensuring compliance with quality and regulatory standards, requiring a solid technical background and excellent communication skills. **

Salary

Base: $117,000.00 - $184,200.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Comprehensive package including medical, dental, vision, 401(k), and paid time off

Skills & Requirements

Must-have

  • 5 years relevant industrial experience
  • GMP Pharmaceutical Environment experience
  • Equipment qualification and process validation
  • Root cause analysis investigations
  • Technical leadership and project management

Nice-to-have

  • Lean Six Sigma tools experience
  • Medical Devices and Combination products knowledge
  • Literature review for new technologies
  • Strong analytical and communication skills
  • Experience with FDA observation preparation

Key Requirements

  • Bachelor's degree in Engineering or related field
  • Minimum 5 years relevant industrial experience
  • Experience in GMP Pharmaceutical Environment
  • US and Puerto Rico Residents Only
  • No VISA Sponsorship available

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter