Sr. Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (onsite)

29

Rahway, New Jersey, USA
Base: $117,000.00 - $184,200.00; bonus/equity: eli...
Hybrid (3 days onsite, 1 day remote)
Oral solid dosage manufacturing
Gmp and safety compliance
Design of experiments (doe)
The job posting is for a Sr. Specialist in Process Engineering at a clinical manufacturing facility in Rahway, New Jersey. The ideal candidate will lead batch manufacturing processes, ensure compliance with GMP standards, and drive innovation in oral solid dosage manufacturing

Job Summary

  • The Non-Sterile Process Engineering team ensures right-first-time manufacture and delivery of high-quality drug products, leveraging pharmaceutical unit operations.
  • This person will lead on-the-floor batch manufacturing in a pilot plant while prioritizing and ensuring safety and quality of clinical supplies.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable, and a comprehensive package of benefits.

Matching Summary

Match Score: 85

The job posting is for a Sr. Specialist in Process Engineering at a clinical manufacturing facility in Rahway, New Jersey. The ideal candidate will lead batch manufacturing processes, ensure compliance with GMP standards, and drive innovation in oral solid dosage manufacturing.

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, sick days

Skills & Requirements

Must-have

  • Oral Solid Dosage manufacturing
  • GMP and safety compliance
  • Design of Experiments (DOE)
  • Lead on-the-floor batch manufacturing
  • GxP documentation authoring and review

Nice-to-have

  • Foster culture of collaboration, learning and innovation
  • Develop and leverage relationships across work groups
  • Propose new, innovative approaches
  • Desire to build new capabilities

Key Requirements

  • Minimum 5 years relevant experience with BS
  • Minimum 3 years relevant experience with MS
  • PhD degree (expected completion by June 2026)
  • Familiarity with GMP and safety compliance regulations
  • Ability to work effectively with diverse skill sets

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter