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

Mayoly

Rahway, New Jersey, USA
Base: $117,000.00 - $184,200.00; bonus/equity: ann...
Hybrid (3 days onsite, 1 day remote)
Oral solid dosage manufacturing
Gxp documentation authoring
Pilot plant batch manufacturing
Mayoly is seeking a Sr. Specialist in Process Engineering for its Oral Solid Dosage team at the FLEx Center in Rahway, NJ. The role involves leading clinical supply manufacturing, ensuring safety and quality, and supporting process development in a GMP environment

Job Summary

  • The Non-Sterile Process Engineering team ensures right-first-time manufacture and delivery of high-quality drug products.
  • 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

Mayoly is seeking a Sr. Specialist in Process Engineering for its Oral Solid Dosage team at the FLEx Center in Rahway, NJ. The role involves leading clinical supply manufacturing, ensuring safety and quality, and supporting process development in a GMP environment.

Salary

Base: $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, including 401(k), paid holidays, vacation, and compassionate and sick days

Skills & Requirements

Must-have

  • Oral Solid Dosage manufacturing
  • GxP documentation authoring
  • Pilot plant batch manufacturing
  • Process development support
  • Design of Experiments application

Nice-to-have

  • Foster culture of collaboration
  • Innovative approach to problems
  • Build partnerships across teams
  • Desire to build new capabilities

Key Requirements

  • Bachelor of Science degree with 5 years experience
  • Master's degree with 3 years experience
  • PhD degree (expected completion by June 2026)
  • Familiarity with GMP and safety regulations
  • Ability to work with diverse skill sets

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter