Engineering Specialist - Commissioning, Qualification, And Validation (cqv)

Our Company

Rahway, NJ, US
Base: $87,300.00 - $137,400.00; bonus/equity: elig...
Hybrid
Cgmp and good documentation practices
Pharmaceutical manufacturing plant operations
Commissioning and qualification/validation
The Engineering Specialist is responsible for Commissioning, Qualification, and Validation (CQV) and broader engineering support across non-sterile operations

Job Summary

  • The Engineering Specialist is responsible for Commissioning, Qualification, and Validation (CQV) and broader engineering support across non-sterile operations.
  • Responsibilities include coaching personnel in Good Documentation Practice and performing risk-based methodologies to assess GMP criticality.
  • Joining this team offers meaningful opportunities for Talent Growth and to make a sustained impact on product reliability and patient safety.

Matching Summary

The Engineering Specialist is responsible for Commissioning, Qualification, and Validation (CQV) and broader engineering support across non-sterile operations.

Salary

Base: $87,300.00 - $137,400.00; Bonus/Equity: eligible for annual bonus and long-term incentive; Benefits: medical, dental, vision, 401(k), paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • cGMP and Good Documentation Practices
  • pharmaceutical manufacturing plant operations
  • commissioning and qualification/validation
  • CMMS and CCMS familiarity
  • Quality and Facilities work flexibility
  • organizational and communication skills

Nice-to-have

  • proactively drive sound decisions
  • demonstrate strong ownership
  • continuous improvement initiatives
  • Lean, Six Sigma experience

Key Requirements

  • Bachelor's Degree in Engineering or Science
  • minimum of 2 years qualification/validation experience
  • familiarity with Quality and cGMP policies
  • experience with CMMS/CCMS systems

Work Rights

Not specified

Tailored Resume

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