The Sterile Drug Product Commercialization group provides technical process leadership and laboratory capabilities for late stage and commercial drug product processes for large molecule and sterile Pharmaceutical products
Job Summary
The Sterile Drug Product Commercialization group provides technical process leadership and laboratory capabilities for late stage and commercial drug product processes for large molecule and sterile Pharmaceutical products.
Responsibilities include serving on cross-functional drug product working groups, supporting activities through filing and Process Performance Qualification (PPQ), and ensuring commercialization programs meet requirements related to science, quality, reliability, schedule, and cost.
The company offers a comprehensive package of benefits including medical, dental, vision healthcare, retirement benefits, paid holidays, vacation, and sick days.
Matching Summary
The Sterile Drug Product Commercialization group provides technical process leadership and laboratory capabilities for late stage and commercial drug product processes for large molecule and sterile Pharmaceutical products.
Salary
Base: $87,300.00 - $137,400.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Comprehensive package including medical, dental, vision, 401(k), paid holidays, vacation, and sick days
Skills & Requirements
Must-have
Sterile drug product commercialization
Late stage and commercial drug product processes
Process scale up and technology transfer
Process validation and regulatory submissions
Large molecule and sterile pharmaceutical products
Nice-to-have
High performance and innovation culture
Out of the box thinking
Diversity and inclusion
Key Requirements
B.S. in relevant field with 2 years of experience or Master's degree
Excellent oral and written communication skills
Ability to articulate process science understanding
Technical experience in large molecules drug product fill finish
Working knowledge of cGMPs for sterile dosage forms