Job Summary

• The Bioprocess Engineer II/III, Upstream supports the planning, execution, and sustained operation of on-site gene therapy manufacturing.
• This role performs hands-on upstream/cell expansion activities to meet production schedules, ensuring materials are manufactured safely and in compliance with cGMP, site quality standards, and applicable environmental, health, and safety requirements.
• US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits.

Matching Summary

Salary

$66,800.00 - $124,000.00; Performance-based cash incentive and potential equity awards; Comprehensive benefits package including health, life, disability, 401(k), and generous time off

Skills & Requirements

Key Requirements

• 3+ years cGMP experience in biologics manufacturing
• 4+ years cGMP experience in biologics manufacturing (in lieu of degree)
• 1+ year experience in Novartis Gene Therapies product manufacture
• 3+ years experience in Novartis Gene Therapies product manufacture (for III)
• Ability to lift/move materials up to 35 lbs
• Working knowledge of cGMP principles and data integrity

Work Rights