Job Summary

• This role will act as a decision maker in the Operations Team, with responsibilities to develop and own set-up of supply chain technology and processes for a new facility design.
• By collaborating with various other functions (MSAT, R&D, Engineering, quality assurance, quality control, health and safety, information technology, operations, planning, etc.) you will ensure the successful transfer of the CAR-T process, the timely start of clinical/commercial manufacturing, and scale out of the facility.
• The overall goal is creation of a compliant, reliable, and cost competitive commercial facility.

Matching Summary

Salary

Base: 94,000-144,500; Bonus/Equity: Not specified; Benefits: Vacation –120 hours per calendar year, Sick time - 40 hours per calendar year, Holiday pay –13 days per calendar year, Work, Personal and Family Time - up to 40 hours per calendar year, Parental Leave – 480 hours, Condolence Leave – 30 days, Caregiver Leave – 10 days, Volunteer Leave – 4 days, Military Spouse Time-Off – 80 hours

Skills & Requirements

Key Requirements

• Minimum 4 years of relevant work experience
• Bachelor's or equivalent experience in Engineering, Bioscience Engineering, Industrial Engineering, Pharmacy, Biochemistry or related field
• Experience in cGMP manufacturing, operations technology development, tech transfer, process and equipment validation, and/or quality management

Work Rights