Senior Director, Supply Chain

Scorpion Therapeutics; Bridgewater (MA); On-site; USD 90,000 - 250,000; Full time

Benefits offered by this job

Competitive base salary

Subsidized Medical, Dental, and Vision Plans

401(k) Matching

Onsite lunches

Stock options

Job summary

A biotech company based in Bridgewater is seeking a Senior Director of Supply Chain to lead the development and execution of a comprehensive supply chain strategy. This role demands 15+ years of experience in a cGMP environment, proven leadership skills, and the ability to manage shifting priorities in a fast-paced setting. Responsibilities include overseeing patient supply and material planning, collaborating with cross-functional teams, and ensuring compliance with quality standards. The position offers a competitive salary range of $90,000 - $250,000, along with excellent benefits.

Qualifications

• 15+ years of experience within a cGMP environment in biotech/biopharma industry.
• 5+ years of leadership experience.
• History of developing cohesive, high performing teams.
• Strong analytical and critical thinking skills.
• Experience with Operational Excellence.

Responsibilities

• Lead and develop an effective Supply Chain organization.
• Establish a robust Global S&OP.
• Oversee implementation of sourcing and procurement strategy.
• Monitor performance against supply chain objectives.
• Build stakeholder relationships across the organization.

Skills

Leadership

Problem solving

Analytical skills

Team building

Communication skills

Lean Manufacturing

Education

Bachelor's degree in supply chain, life science, engineering, or related field

Tools

ERP systems

Job description

We are seeking a highly motivated Senior Director, Supply Chain reporting to our VP of Operations who will lead and oversee the buildout of our Supply Chain organization. This individual will be responsible for developing and implementing a comprehensive Supply Chain Management strategy and business processes that will allow the organization to scale effectively and meet the needs of internal and external stakeholders and customers. This individual will oversee patient supply and material planning, materials management, inventory control, product tracking (chain of identity and chain of custody), import/export permits, shipping/receiving, and cold chain logistics of personalized cell therapies throughout our manufacturing network. This individual will also be responsible for interpreting and analyzing demand and usage requirements of various operating supplies, general and critical raw materials, components, equipment, and maintenance supplies. This is a multidisciplinary role and requires proven leadership to drive effective communication, coordination, and collaboration across relevant cross functional groups at all levels of the organization, including Manufacturing, Quality, MS&T, QC, Process/Analytical Development, Training, Engineering/Facilities, HS&E, Finance, IT, and Commercial Sales. The successful candidate should enjoy working in a fast‑paced, mission‑driven environment, and be prepared to tackle a broad selection of challenges as the company grows.

Responsibilities

• Lead, direct, coach, and develop an effective Supply Chain organization supporting the manufacture and release of autologous and allogeneic cell therapy products across a matrixed manufacturing network by developing, implementing, and executing strategic Supply Chain Management business processes
• Lead the Supply Chain organization by effectively interfacing and collaborating with key stakeholders and functions to drive business transformation and process optimization at all levels across the organization
• Develop and continually update efficient business processes for GMP production planning, production, supply chain management, warehousing, and distribution of finished product and raw materials
• Establish a robust Global S&OP that incorporates multi-product, multi-client production and material planning business processes across our manufacturing network by working closely with relevant business stakeholders
• Oversee the implementation of the Cellares corporate sourcing and procurement strategy by establishing robust processes and procedures, including the evaluation, selection, and implementation of an enterprise‑wide ERP solution
• Oversee the creation and execution of an overall Supply Chain systems roadmap for the organization in close collaboration with relevant stakeholders
• Create and implement tools and processes for clinical trials and future commercial requirements from apheresis operations/collection to infusion incorporating logistics, Chain of Custody (COC), Chain of Identity (COI), real time scheduling and tracking, and capacity management
• Champion quality, safety, and compliance culture; demonstrate critical thinking skills and high reliability mentality, ensure work is completed according to cGMP guidelines and business procedures
• Build Operational Excellence capabilities through training, and continuous improvement tools and events such as 5S assessment and Kaizen, applying boots on the ground and digitalization approaches
• Accountable for monitoring the performance of the supply chain organization and the manufacturing network with respect to local and integrated supply chain network objectives
• Work closely with other functional areas to develop and execute against the strategic plan for our manufacturing network
• Establish key stakeholder relationships with internal and external stakeholders

Requirements

• Bachelor's degree in supply chain, life science, engineering, or related field required
• 15+ years of experience within a cGMP environment in the biotech/biopharma industry (operations, supply chain, manufacturing, ERP, digital/data technologies, or quality) with 10 years of Supply Chain support
• 5+ years of leadership experience with 5+ years of experience supporting ERP systems
• Cell/Gene Therapy or CDMO experience preferred
• Ability to build strong partnerships and effectively integrate with external collaborators to drive projects/programs forward in a matrixed environment
• Must be able to manage shifting priorities to meet critical deadlines in a fast paced and dynamic, growing environment, while providing clear direction to team members
• History of developing and building cohesive, high performing teams with a strong sense of mission, providing training and mentoring to build sufficient management depth throughout the organization and ensure strong succession planning
• Strong analytical, problem solving and critical thinking skills and the ability to lead as a change agent to promote flexibility, creativity, and accountability
• Excellent teamwork and interpersonal skills with ability to influence and build strong working relationships at all levels within the organization
• Experience with Operational Excellence and/or Lean Manufacturing
• Excellent organizational and communication skills
• Self‑motivated and passionate about advancing the field of cell therapy
• Self‑awareness, integrity, authenticity, and a growth mindset

$90,000 - $250,000 a year

Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.

This is Cellares

Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life‑saving cell therapies. The company’s Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high‑throughput platform that delivers true walk‑away, end‑to‑end automation. Cell Shuttles will be deployed in Cellares’ Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.

The company is headquartered in South San Francisco, California with its commercial‑scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world‑class investors and has raised over $355 million in financing.

Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.