Sr. Specialist, Engineering (onsite)

Merck & Co., Inc., Rahway, NJ, USA

Rahway, New Jersey, USA
Base: $117,000.00 - $184,200.00; bonus/equity: eli...
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Cgmp manufacturing experience
Specialty dosage forms
Oral solid dosage
** Merck & Co., Inc. is seeking a Sr. Specialist in Engineering for their Rahway, NJ facility to lead manufacturing engineering operations for specialty dosage forms and oral solid dosage (OSD) production on the second shift. The ideal candidate will have extensive GMP experience and be responsible for technical decision-making, safety compliance, and team development. **

Job Summary

  • The Rahway FLEx Center is seeking a Manufacturing Engineering Lead to support specialty dosage forms and oral solid dosage (OSD) GMP development activities on second shift.
  • The role involves serving as the technical lead for shift production, coordinating safety, quality, and equipment decisions, and evaluating performance to protect patients, people, and compliance.
  • The successful candidate will own technical decisions, lead room and equipment readiness, author GMP documentation, troubleshoot issues, and coach the shift team.

Matching Summary

Match Score: 75

** Merck & Co., Inc. is seeking a Sr. Specialist in Engineering for their Rahway, NJ facility to lead manufacturing engineering operations for specialty dosage forms and oral solid dosage (OSD) production on the second shift. The ideal candidate will have extensive GMP experience and be responsible for technical decision-making, safety compliance, and team development. **

Salary

Base: $117,000.00 - $184,200.00; Bonus/Equity: eligible for annual bonus and long-term incentive; Benefits: comprehensive package including medical, dental, vision, retirement, paid holidays, vacation, compassionate and sick days

Skills & Requirements

Must-have

  • cGMP manufacturing experience
  • specialty dosage forms
  • oral solid dosage
  • technical decision making
  • equipment troubleshooting
  • root-cause analysis

Nice-to-have

  • champion ways of working
  • continuous improvement
  • knowledge sharing
  • team development

Key Requirements

  • Bachelor’s degree in Engineering or Science or equivalent GMP manufacturing experience
  • 5+ years in GMP clinical or commercial manufacturing
  • Demonstrated knowledge of cGMP, data integrity, batch documentation, investigations, and CAPA
  • Experience with specialty equipment (e.g., spray dryers, autoinjector assemblies, isolators)
  • Ability to work second shift on-site

Work Rights

Not specified

Tailored Resume

Cover Letter