Associate Director, Supply Chain Operations

Summary:
Cartesian Therapeutics is reimagining cell therapies with transformative technologies to bring a new generation of treatment options to patients with autoimmune diseases. The Associate Director, Supply Chain Operations will be part of Cartesian's Supply Chain team and manage day to day enterprise-level supply chain operations.

Key Responsibilities

• Management of Supply Chain Operations: Oversee day-to-day warehouse and manufacturing support GMP operations and personnel. Support clinical, QC, and R&D supply chain teams when necessary. Responsible for internal supply chain budget, order placement and inventory management.
• Compliance: Develop, draft and implement supply chain processes and policies consistent with safety policies, quality systems, and cGMP requirements. Principal contact for supply chain in internal and external audits. Responsible for manufacturing lot traceability and chain of custody. Initiate and/or lead supply chain-related deviations, CAPAs, and change controls.
• Collaboration: Build strong partnerships with Manufacturing, Clinical, Quality Control, Quality, and Finance/Accounting and work as part of a cross-functional team.
• Continuous Improvement / Operational Excellence: Responsible for tracking and reporting on key performance indicators (KPIs). Identify and implement supply chain process improvements.

Qualifications

• Associate or bachelor's degree in a scientific or health services field.
• A minimum of 10 years of Operations experience within a cGMP environment in the biotech/biopharma industry. Experience in cell therapy operations preferred.
• Experience effectively managing warehouse and supply chain personnel.
• Proficient computer skills to be able to navigate specialized software and databases.
• An ability to build strong external partnerships and effectively integrate cross-functionally to drive projects/programs forward.
• Ability to work independently and successfully, prioritize and manage multiple tasks simultaneously, integrate cross-functional issues and balance competing priorities effectively.
• Clear and succinct verbal and written communication skills with an attention to detail and the ability to follow procedures. Experience writing SOPs and quality events.
• Knowledge of cGMP regulations and FDA guidance related to manufacturing of cell based products.
• Ability to lift a minimum of 50 lbs. and stand for a long period of time.
• Sufficient vision and hearing capability to work in job environment with physical dexterity sufficient to use computers and document production records.
• Ability to handle human derived materials in BSL-2 facility.
• Physical dexterity sufficient to use computers and documentation.

At Cartesian Therapeutics, we are committed to transparency and equity in our compensation practices. The salary range for this position is $160,000to $190,000 per year. Please note that the final salary will be determined based on several factors, including but not limited to years of experience, industry experience, education, and specific skills relevant to the role. We believe in rewarding our team members fairly and encourage open discussions about compensation throughout the hiring process.

Cartesian is an Equal Opportunity Employer and is committed to fostering an environment in which all employees are treated fairly without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, ancestry, disability, marital status, genetic information, military status, or any other characteristic protected under applicable law.