The successful candidate will join a fast-paced, multidisciplinary team supporting commercial pharmaceutical products to ensure undisrupted supply globally
Job Summary
The successful candidate will join a fast-paced, multidisciplinary team supporting commercial pharmaceutical products to ensure undisrupted supply globally.
Responsibilities include leading analytical method development, authoring regulatory documents, performing investigations, and supporting inspections and audits.
The role offers a comprehensive benefits package including medical, dental, vision, retirement plans, paid holidays, vacation, and eligibility for annual bonus and long-term incentives.
Matching Summary
The successful candidate will join a fast-paced, multidisciplinary team supporting commercial pharmaceutical products to ensure undisrupted supply globally.
Salary
Base: $142,400.00 - $224,100.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision, retirement, paid holidays, vacation
Skills & Requirements
Must-have
Analytical method development and validation
Technical troubleshooting skills
GMP compliance in commercial manufacturing
Chromatography and spectroscopy techniques
Regulatory submission documentation
Interdisciplinary team collaboration
Nice-to-have
Strategic thinking and risk management
Knowledge of CMC filing requirements
Experience with pharmaceutical drug substance development
Strong communication and interpersonal skills
Ability to influence team direction
Adaptability to change
Key Requirements
Bachelor’s Degree in Chemistry or related discipline with 10 years experience
Master’s Degree in Chemistry or related discipline with 8 years experience
PhD in Analytical Chemistry or related discipline with 4 years experience
Experience with chromatography, spectroscopy, dissolution, Karl Fischer