Cellares

Senior Director, Supply Chain

Cellares$90K — $250K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in supply chain, life science, engineering, or related field required
  • 15+ years of cGMP experience in biotech/biopharma with 10 years in Supply Chain support
  • 5+ years in leadership roles with ERP system support
  • Preferred experience in Cell/Gene Therapy or Contract Development and Manufacturing Organizations (CDMO)
  • Strong problem solving and analytical skills with a record of driving change and fostering accountability

Responsibilities

  • Lead the development and execution of a strategic Supply Chain Management strategy across a matrix manufacturing network
  • Collaborate with stakeholders to drive process optimization and business transformation
  • Design and optimize business processes for GMP production planning and supply chain management
  • Establish a Global Sales and Operations Planning (S&OP) framework for multi-product planning
  • Oversee corporate sourcing and procurement strategy implementations, including ERP solution selection
  • Manage the Supply Chain systems roadmap creation in collaboration with stakeholders
  • Develop tools for clinical trials logistics and infused patient supply tracking

Benefits

  • Highly subsidized Medical, Dental, and Vision Plans
  • 401(k) Matching
  • Onsite lunches
  • Stock options
Full 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.

About Cellares

Cellares is a biotechnology company that is developing a platform for automated cell engineering. The platform uses advanced robotics and machine learning algorithms to streamline the process of cell engineering, making it faster, more efficient, and more cost-effective. Cellares' technology has a wide range of potential applications, including the development of new cell therapies for cancer and other diseases. The company was founded in 2018 and is based in San Francisco, California.
Learn more about Cellares
Size
50 employees
Industry
Founded
2018

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