Manager, Engineering - 2nd Shift (onsite)

Vetamc

Rahway, New Jersey, USA
$117,000.00 - $184,200.00; bonus/equity: annual bo...
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Sterile drug product manufacturing
Gmp clinical manufacturing
Continuous improvement culture
** Vetamc is seeking a Manager of Engineering for their 2nd shift operations at their Rahway, New Jersey facility, which focuses on sterile production within a new multi-modality drug product development plant. The role involves managing a team of technicians, ensuring compliance with GMP standards, and fostering a culture of continuous improvement. **

Job Summary

  • The Sterile Production Supervisor manages a team of technicians for daily operations, ensuring shift objectives are achieved while reliably supplying quality product at a competitive cost.
  • This role is responsible for creating and sustaining a culture that ensures compliance (Safety, Environment, cGMP, etc.) are imperatives for the business and for developing a company Production System (MPS) and continuous improvement culture.
  • The company offers a comprehensive package of benefits including medical, dental, vision healthcare, retirement benefits, paid holidays, vacation, and compassionate and sick days.

Matching Summary

Match Score: 75

** Vetamc is seeking a Manager of Engineering for their 2nd shift operations at their Rahway, New Jersey facility, which focuses on sterile production within a new multi-modality drug product development plant. The role involves managing a team of technicians, ensuring compliance with GMP standards, and fostering a culture of continuous improvement. **

Salary

$117,000.00 - $184,200.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; 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

  • Sterile drug product manufacturing
  • GMP clinical manufacturing
  • Continuous improvement culture
  • Compliance with regulations

Nice-to-have

  • High performance coaching
  • Servant leader
  • Engaged workforce
  • Respectfully challenge thinking

Key Requirements

  • Bachelor’s Degree or 7 years pharmaceutical manufacturing experience
  • 4 years experience in operations management, Quality, Technical Operations, Technology, Engineering or Maintenance
  • 2 years aseptic/sterile drug product manufacturing experience
  • 2 years heavily regulated industry experience
  • 2 years direct supervisory experience

Work Rights

Not specified

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