The successful candidate will join a multidisciplinary team to support commercial pharmaceutical products ensuring undisrupted supply globally
Job Summary
The successful candidate will join a multidisciplinary team to support commercial pharmaceutical products ensuring undisrupted supply globally.
Responsibilities include leading analytical method development, authoring regulatory documents, and providing technical support during inspections and audits.
The company offers a comprehensive benefits package including medical, dental, vision, retirement plans, paid holidays, and vacation.
Matching Summary
The successful candidate will join a multidisciplinary team to support commercial pharmaceutical products ensuring undisrupted 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, paid holidays and vacation
Skills & Requirements
Must-have
Analytical method development and validation
Pharmaceutical GMP compliance
Technical troubleshooting skills
Chromatography and spectroscopy techniques
Data integrity management
Interdisciplinary team collaboration
Nice-to-have
Strategic thinking and risk management
Regulatory submission documentation
Knowledge of CMC filing requirements
Experience with pharmaceutical commercialization
Strong verbal and written communication
Ability to influence team direction
Key Requirements
Bachelor’s Degree in Chemistry or related discipline with 10+ years experience
Master’s Degree with 8+ years experience or PhD with 4+ years experience
Experience in pharmaceutical development and GMP compliance