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

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Rahway, NJ, US
Base: $87,300.00 - $137,400.00; bonus/equity: elig...
Hybrid
Commissioning and qualification/validation
Good manufacturing practices (gmp)
Computerized maintenance management systems (cmms)
The Engineering Specialist leads CQV development and execution for new and modified processing equipment, systems, and critical utilities in pharmaceutical operations

Job Summary

  • The Engineering Specialist leads CQV development and execution for new and modified processing equipment, systems, and critical utilities in pharmaceutical operations.
  • Joining this team offers meaningful opportunities for Talent Growth and to make a sustained impact on product reliability and patient safety to continue advancing our mission.
  • The role is based in Rahway, NJ, with potential travel to West Point, PA, and offers a comprehensive benefits package including medical, dental, vision, retirement, paid holidays, and vacation.

Matching Summary

The Engineering Specialist leads CQV development and execution for new and modified processing equipment, systems, and critical utilities in pharmaceutical operations.

Salary

Base: $87,300.00 - $137,400.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision, retirement, paid holidays, vacation

Skills & Requirements

Must-have

  • Commissioning and qualification/validation
  • Good Manufacturing Practices (GMP)
  • Computerized Maintenance Management Systems (CMMS)
  • Good Documentation Practices
  • Equipment commissioning and validation
  • Process engineering and optimization

Nice-to-have

  • Experience with Kneat paperless validation
  • SAP Plant Maintenance experience
  • Lean and Six Sigma methodologies
  • Strong organizational and communication skills
  • Ability to work independently and lead tasks

Key Requirements

  • Bachelor's Degree in Engineering or Science
  • Minimum 2 years qualification/validation experience
  • Experience with GMP pharmaceutical manufacturing
  • Familiarity with Quality and cGMP policies
  • Experience with CMMS and CCMS systems

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter