This person will work on the preparation, and support execution, of pilot-scale campaigns for the Good Manufacturing Practice (GMP) manufacture of bulk vaccine and biologics clinical drug substance supplies
Job Summary
This person will work on the preparation, and support execution, of pilot-scale campaigns for the Good Manufacturing Practice (GMP) manufacture of bulk vaccine and biologics clinical drug substance supplies.
Collaborate in multi-disciplinary project teams to ensure seamless technology transfer of vaccine and biologic processes.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
Matching Summary
This person will work on the preparation, and support execution, of pilot-scale campaigns for the Good Manufacturing Practice (GMP) manufacture of bulk vaccine and biologics clinical drug substance supplies.
Salary
Base: $87,300.00 - $137,400.00; 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 manufacturing of biologics
Process development activities
cGMP, Quality Systems, and safety
Fast-paced and dynamic setting
Prepare and review critical documentation
Nice-to-have
Organizational, problem-solving skills
Project management skills
Technical background in unit operations
Leading small teams in a matrixed organization
Key Requirements
Bachelor’s degree in Chemical Engineering, Biological Sciences or related field with 2 full years of relevant experience
Master’s degree with 1+ years of relevant experience