Quality Assurance At-the-Source Specialist, Cell Therapy

. Typical Accountabilities

• Maintain a consistent Quality presence in manufacturing areas and provide real-time, practical guidance that supports safe, compliant, and reliable execution.
• Support manufacturing unit operations from a Quality Assurance perspective and assist to resolve manufacturing events and/or quality events in real-time
• Independently assess routine and moderately complex quality situations, integrate available facts and risk considerations, and determine appropriate action or escalation within established standards.
• Partner across functions to clarify requirements, align decisions, remove barriers, and sustain appropriate Quality independence.
• Recognize emerging risks, recurring issues, and performance gaps; communicate implications and recommend proportionate actions.
• Lead defined problem-solving and improvement activities, ensuring decisions are evidence-based, clearly documented, and carried through to effective resolution.
• Coach colleagues on quality thinking, disciplined execution, data integrity, contamination control, and right-first-time behaviors.
• Contribute quality judgment to operational meetings, shift handoffs, readiness discussions, and cross-functional decision forums.
• Manage multiple priorities independently, communicate changes in risk or urgency, and maintain reliable follow-through in a fast-paced patient-focused environment.
• Support inspection readiness and represent Quality confidently within the scope of training, experience, and delegated authority.
• Work a shift-based schedule of four days per week, Wednesday through Saturday, and support occasional off-hours or holidays as needed for manufacturing operations and patient commitments.
• The role may require additional responsibilities as necessary.

• Bachelor's degree in Science, Engineering, Quality, or a related technical field with relevant GMP quality or manufacturing experience; equivalent combinations of education and experience may be considered in accordance with the approved job catalogue.
• Demonstrated ability to work independently in a regulated environment and apply cGMP principles to real-time operational decisions.
• Sound risk-based judgment, including the ability to distinguish routine issues from situations requiring broader escalation.
• Ability to lead defined problem-solving, synthesize facts, recommend actions, and communicate decisions clearly.
• Strong cross-functional collaboration and influencing skills, including respectful challenge and practical coaching.
• Ability to organize competing priorities and deliver high-quality work with limited day-to-day supervision.
• Ability to gown and work in controlled manufacturing environments.
• Ability to work the established four-day Wednesday-through-Saturday shift schedule and meet the additional scheduling requirements of the role.

• Experience in biologics, aseptic processing, advanced therapies, or autologous cell therapy manufacturing.
• Working knowledge of international cell therapy GxP regulatory frameworks, regulations, and guidance.
• Experience with digital manufacturing, document management, learning, or quality systems.

The annual base pay for this position ranges from $100,880 - $151,321. Our positions offer eligibility for multiple incentives an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans .