Associate Director, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (onsite)

Vetamc

Rahway, New Jersey, US
$142,400.00 - $224,100.00; bonus + long-term incen...
**
Gmp manufacturing operations
Oral solid dosage processing
Process robustness assessments
** Vetamc is seeking an Associate Director of Process Engineering for its FLEx Center in Rahway, New Jersey. The role focuses on leading the clinical manufacturing of oral solid dosage forms and requires extensive experience in GMP processes, team mentorship, and technical project management. **

Job Summary

  • The Non-Sterile Process Engineering team ensures right-first-time manufacture and delivery of high-quality drug products, leveraging pharmaceutical unit operations such as spray-drying, hot-melt extrusion, blending, roller compaction, encapsulation, compression, and film coating.
  • Lead and strategically plan on-the-floor batch manufacturing to ensure safety and quality of clinical supplies to augment and accelerate our products.
  • Mentor a team of 2-5 process engineers by technical coaching and developing for success through feedback and development guidance.

Matching Summary

Match Score: 75

** Vetamc is seeking an Associate Director of Process Engineering for its FLEx Center in Rahway, New Jersey. The role focuses on leading the clinical manufacturing of oral solid dosage forms and requires extensive experience in GMP processes, team mentorship, and technical project management. **

Salary

$142,400.00 - $224,100.00; Bonus and Long-Term Incentive eligible; Comprehensive benefits package

Skills & Requirements

Must-have

  • GMP manufacturing operations
  • Oral Solid Dosage processing
  • Process robustness assessments
  • Root cause analysis
  • Deviation management
  • cGMP, FDA, EMA regulatory requirements

Nice-to-have

  • Subject matter expert in drug delivery
  • Experience in Formulation Sciences
  • Experience in Analytical Sciences
  • Experience with spray dried intermediates
  • Experience with hot melt extrusion
  • Technical transfer of early-phase drug product

Key Requirements

  • Bachelor of Science degree with 10 years relevant experience
  • Master’s degree with 8 years relevant experience
  • PhD degree with 4 years relevant experience
  • Experience authoring, reviewing, and approving GMP documentation
  • Experience managing and developing teams

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter