Sr. Spclst, Engineering (2nd Shift) - Onsite

Merck & Co., Inc.

Rahway, NJ, USA
Base: $117,000.00 - $184,200.00; bonus/equity: eli...
Onsite (2nd shift)
Bs or ms in engineering with 5 years experience
Expertise in sterile processing equipment
Knowledge of plc, dcs, and mes automation systems
Merck & Co., Inc. is seeking a Senior Specialist in Engineering for their second shift operations at the FLEx Sterile facility in Rahway, NJ. The role involves supporting production operations through troubleshooting, process development, and continuous improvement projects, requiring a strong background in sterile processing and technical operations

Job Summary

  • The role supports the FLEx Sterile facility's mission to deliver compliant, high-quality clinical supplies for diverse product modalities including biologics and vaccines.
  • Candidates will collaborate closely with Production, Quality, and Facilities teams to ensure right-first-time execution and timely delivery of business goals.
  • The position offers a comprehensive benefits package including medical, dental, vision, 401(k), and eligibility for annual bonuses and long-term incentives.

Matching Summary

Match Score: 85

Merck & Co., Inc. is seeking a Senior Specialist in Engineering for their second shift operations at the FLEx Sterile facility in Rahway, NJ. The role involves supporting production operations through troubleshooting, process development, and continuous improvement projects, requiring a strong background in sterile processing and technical operations.

Salary

Base: $117,000.00 - $184,200.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • BS or MS in Engineering with 5 years experience
  • Expertise in sterile processing equipment
  • Knowledge of PLC, DCS, and MES automation systems
  • Experience with aseptic processing techniques
  • Familiarity with US and EU GMP regulations
  • Ability to prepare SOPs and GXP documents
  • Lean Six Sigma Green Belt certification

Nice-to-have

  • Commissioning, Qualification and Validation experience
  • Understanding of ISA88 and ISA95 principles
  • Knowledge of Investigational drug regulatory requirements
  • Lean Six Sigma Black Belt certification
  • Strong project management and critical thinking skills
  • Willingness to learn and lead in a growth mindset

Key Requirements

  • BS or MS in Chemical, Mechanical, or Biomedical Engineering
  • Minimum 5 years of relevant engineering experience
  • Lean Six Sigma Green Belt certification required
  • No visa sponsorship available

Work Rights

Not specified

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