Manufacturing Execution System (mes) Specialist - 2nd Shift

39med

Rahway, New Jersey, US
Base: $87,300.00 - $137,400.00; bonus/equity: elig...
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Mes system support and troubleshooting
Gmp manufacturing environment experience
Collaborate with cross-functional teams
** 39med is seeking a Manufacturing Execution System (MES) Specialist for their new FLEx Center in Rahway, NJ, to support the deployment and management of MES in a GMP manufacturing environment. The ideal candidate will have a background in engineering or pharmaceutical sciences, along with experience in MES systems and GMP compliance. **

Job Summary

  • The FLEx Center is a new multi-modality drug product development and GMP clinical manufacturing plant focused on speed, agility, and rigor.
  • The MES Specialist will support the deployment and sustainment of a Manufacturing Execution System (MES) to enable Electronic Batch Records, Electronic Logs, and Weigh & Dispense functionality.
  • This role offers an opportunity to become an MES expert while learning about clinical drug product processing in both Sterile and Non-Sterile modalities.

Matching Summary

Match Score: 75

** 39med is seeking a Manufacturing Execution System (MES) Specialist for their new FLEx Center in Rahway, NJ, to support the deployment and management of MES in a GMP manufacturing environment. The ideal candidate will have a background in engineering or pharmaceutical sciences, along with experience in MES systems and GMP compliance. **

Salary

Base: $87,300.00 - $137,400.00; 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

  • MES system support and troubleshooting
  • GMP manufacturing environment experience
  • Collaborate with cross-functional teams
  • Develop and sustain MES Digital Records
  • Execute change control processes
  • Prepare Standard Operating Procedures

Nice-to-have

  • Continuous process improvement identification
  • Knowledge of Quality Systems and Regulatory Standards
  • SAP integration and master data expertise
  • Share best practices across network sites
  • Assist in agency inspections

Key Requirements

  • Minimum 2 years GMP manufacturing experience
  • B.A./B.S. degree in Engineering, Pharmaceutical Sciences, Business, or equivalent
  • Ability to don required gowning and PPE

Work Rights

Not specified

Tailored Resume

Cover Letter