Sr. Specialist, Engineering (onsite)

Laboratory Animal Management Association

New Jersey, United States
$117,000.00 - $184,200.00; bonus/equity: eligible ...
On-site
Gmp development activities
Technical lead for shift production
Evaluate safety, quality, and equipment
The Laboratory Animal Management Association is seeking a Sr. Specialist, Engineering to lead manufacturing engineering on the second shift at their Rahway FLEx Center in New Jersey. The role involves overseeing production safety, quality, and equipment performance in GMP settings, with a strong emphasis on technical leadership and problem-solving

Job Summary

  • The successful incumbent will serve as the technical lead for shift production, coordinating safety, quality, and equipment decisions.
  • This role evaluates safety, product/process quality, and equipment performance and determines the appropriate path forward to protect patients, people, and compliance.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

Matching Summary

Match Score: 85

The Laboratory Animal Management Association is seeking a Sr. Specialist, Engineering to lead manufacturing engineering on the second shift at their Rahway FLEx Center in New Jersey. The role involves overseeing production safety, quality, and equipment performance in GMP settings, with a strong emphasis on technical leadership and problem-solving.

Salary

$117,000.00 - $184,200.00; Bonus/Equity: eligible for annual bonus and long-term incentive; Benefits: medical, dental, vision healthcare and other insurance benefits, retirement benefits, 401(k), paid holidays, vacation, and compassionate and sick days

Skills & Requirements

Must-have

  • GMP development activities
  • technical lead for shift production
  • evaluate safety, quality, and equipment
  • author, execute, and close GMP documentation
  • troubleshoot equipment/system issues
  • lead improvement activities on specialty equipment

Nice-to-have

  • champion ways of working
  • coaching and developing shift team
  • familiarity with TPM/RCM

Key Requirements

  • 5+ years in GMP clinical or commercial manufacturing
  • Bachelor’s degree in Engineering or Science
  • Demonstrated knowledge of cGMP
  • Experience with specialty equipment
  • Ability to work second shift on-site

Work Rights

Not specified

Tailored Resume

Cover Letter