Technical Operations Manager, GMP Engineering and Cell Manufacturing Facility

Summary:

Leads a team of professional associates responsible for the manufacturing of CAR-T and other cell therapies within the GMP Engineering & Cell Manufacturing Facility. Oversees the day-to-day operations of cell therapy programs, including manufacturing and facilities cleaning and maintenance. Coordinates process and analytical development activities, ensuring compliance with cGMP (Good Manufacturing Practice) regulatory standards and safety protocols as well as managing the company’s resources effectively. Ensures efficient production processes and effective analytical strategies and methods, coordinating with different departments, and implementing innovative approaches to improve productivity and profitability. Works closely with the team to provide process, material, and equipment knowledge to meet customer requirements and addresses operational and routine challenges as they arise for manufacturing. Participates and assists Technical Operations management with the preparation of budgets, statements of work, and other documents requested by internal and external customers required for reporting purposes, oversight of operations and for publication. The salary range for this position is $111,387 - $135,829 annually which includes a comprehensive benefits package. The actual offer may vary based on qualifications, skills, and experience.

Qualifications:

Required Education and Experience

1. PhD in a health, life science, engineering, or related field and the equivalent of five (5) years of full-time experience in GMP cell therapy, viral vector, gene therapy, biologics, or related advanced therapy manufacturing, process development, analytical development, quality control, or MSAT, including the equivalent of eighteen (18) months of experience in a supervisory, consultative, managerial, or executive capacity; or
2. Master's degree in a health, life science, engineering, or related field and the equivalent of seven (7) years of full-time experience in GMP cell therapy, viral vector, gene therapy, biologics, or related advanced therapy manufacturing, process development, analytical development, quality control, or MSAT, including the equivalent of eighteen (18) months of experience in a supervisory, consultative, managerial, or executive capacity; or
3. Bachelor's degree in a health, life science, engineering, or related field and the equivalent of nine (9) years of full-time experience in GMP cell therapy, viral vector, gene therapy, biologics, or related advanced therapy manufacturing, process development, analytical development, quality control, or MSAT, including the equivalent of eighteen (18) months of experience in a supervisory, consultative, managerial, or executive capacity.