Principal Scientist, Technical Director - Process Engineering - Oral Solid Dosage, Clinical Manufacturing (onsite)

leHACK

Rahway, New Jersey, US
Base: $173,200.00 - $272,600.00; bonus/equity: eli...
Hybrid (3 days onsite, 1 day remote)
Gmp drug product processing
Oral solid dosage forms
Process robustness & validation
The job posting is for a Principal Scientist / Technical Director in Process Engineering at leHACK, located in Rahway, New Jersey. The role focuses on leading clinical supply manufacturing for oral solid dosage forms while ensuring process robustness and compliance with regulatory standards

Job Summary

  • The Formulation, Laboratory, and Experimentation (FLEx) Center is a multi-modality drug product development and clinical manufacturing facility focusing on non-sterile drug products.
  • The Principal Scientist / Sr. Principal Scientist / Technical Director will lead clinical supply manufacturing, scientific rigor of processes, and drive new technology strategy.
  • This role offers a salary range of $173,200.00 - $272,600.00 and eligibility for annual bonus and long-term incentive, along with a comprehensive benefits package.

Matching Summary

Match Score: 85

The job posting is for a Principal Scientist / Technical Director in Process Engineering at leHACK, located in Rahway, New Jersey. The role focuses on leading clinical supply manufacturing for oral solid dosage forms while ensuring process robustness and compliance with regulatory standards.

Salary

Base: $173,200.00 - $272,600.00; Bonus/Equity: eligible for annual bonus and long-term incentive; 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

  • GMP drug product processing
  • Oral solid dosage forms
  • Process robustness & validation
  • Root cause analysis
  • Deviation management
  • cGMP, FDA, EMA regulatory requirements

Nice-to-have

  • New technology strategy
  • Scientific understanding
  • Capability build
  • Creativity and discipline
  • Enhance professional image

Key Requirements

  • Bachelor of Science degree with 14 years experience
  • Master’s degree with 10 years experience
  • PhD degree with 8 years experience
  • Extensive GMP experience
  • Subject matter expert
  • Experience supporting GMP audits

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter