The successful candidate will join a multidisciplinary team supporting commercial pharmaceutical products to ensure uninterrupted supply globally
Job Summary
The successful candidate will join a multidisciplinary team supporting commercial pharmaceutical products to ensure uninterrupted supply globally.
This role involves leading analytical method development, troubleshooting, and providing documentation support during regulatory inspections and audits.
The company offers a comprehensive benefits package including medical, dental, vision, retirement plans, paid holidays, vacation, and sick days.
Matching Summary
The successful candidate will join a multidisciplinary team supporting commercial pharmaceutical products to ensure uninterrupted supply globally.
Salary
Base: $142,400.00 - $224,100.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Comprehensive medical, dental, vision, retirement, and paid time off
Skills & Requirements
Must-have
Analytical method development and validation
Technical troubleshooting skills
Chromatography and spectroscopy techniques
GMP compliance in commercial manufacturing
Data integrity management
Interdisciplinary team collaboration
Nice-to-have
Strategic thinking and risk management
Knowledge of CMC filing requirements
Experience with regulatory inspections
Ability to influence team direction
Adaptability to change
Strong communication skills
Key Requirements
Bachelor’s degree with 10+ years pharmaceutical experience
Master’s degree with 8+ years pharmaceutical experience
PhD with 4+ years pharmaceutical experience
Experience in pharmaceutical development and GMP compliance
Ability to work in US locations (West Point, PA or Rahway, NJ)