Job Summary

• This role serves as the single accountable lead for end-to-end management of raw materials and GMP supplies supporting pilot-scale clinical bulk manufacturing of vaccines and therapeutic proteins.
• The position requires translating regulatory expectations into procedures while managing validated systems like SAP, RLIMS2, Veeva, and MEDS to ensure data integrity and timely product availability.
• Candidates will drive continuous improvement initiatives to reduce lead times and costs while mentoring staff and reporting risks to senior stakeholders in a fast-paced environment.

Matching Summary

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Key Requirements

• BS, MS, or MBA in Engineering or Biological Sciences
• Minimum 7 years relevant pharmaceutical industry experience
• No visa sponsorship available

Work Rights