External Manufacturing Associate Director

Job Description

Associate Director, Cell & Gene Therapies External Manufacturing Operations - Commercial Manufacturing & Supply Chain, Vertex Pharmaceuticals (based in US, New England)

The primary focus of the Associate Director, External Manufacturing role is to oversee Vertex’s critical cell and gene therapy Contract Manufacturing Organizations (CMOs) and implement our vision for this business‑critical function. We are looking for a candidate with breadth of professional experience and drive to work with internal and external partners to define and manage the ongoing cGMP supply of cell and gene therapy products from clinical through post‑approval lifecycle management.

The right candidate should have the ability to understand challenges and make proactive decisions after anticipating cross‑functional and patient impact. The successful candidate should have a strong operational, quality, compliance and technical background, with proven project management and supplier management abilities. The candidate will be located either at the CMO site and/or be able to travel up to 50% of their time to those sites as a "Person‑in‑Plant" to oversee activities on the ground or as an SME to provide technical support.

The successful candidate will be a key member of the Vertex/CMO Virtual Plant Team (VPT) contributing to broader External Manufacturing group activities.

• Function as the first/primary point of contact for all Vertex interests/activities at ATMP cell and gene therapy Contract Manufacturing Organizations (CMOs).
• Provide operational oversight of, and troubleshooting support to, CMOs to ensure all deliverables meet or exceed Vertex and regulatory requirements (including but not limited to successful execution of manufacturing operations, on‑time shipments, quality compliance and cost management); be Vertex’s "eyes and ears" at the CMO for right‑first‑time execution of commercial operations.
• Proactively "connect the dots" on emerging trends and issues and lead/influence cross‑functional teams to drive resolutions and minimize impact to compliance and delivery of safe and reliable supply.
• Maintain on‑site presence at CMO facilities for extended periods (including off hours/weekends) to oversee (i) critical program activities, (ii) clinical and commercial batch manufacturing until the CMO is sustainably executing operations, and (iii) Health Authority inspections.
• Leverage Technical, Quality and Regulatory SMEs to provide guidance to CMOs and ensure cross‑functional alignment on program priorities and deliverables from clinical through commercial manufacturing and supply.
• Liaise closely with internal and CMO stakeholders and leadership to drive Vertex business operations priorities including but not limited to (i) contract management (including tracking KPIs and metrics e.g. for batch release, inventory targets and schedule attainment), (ii) forecast communication and schedule alignment, (iii) supplier governance (including Vertex Quality/other audits) and (iii) finance (e.g., issuance of POs and reconciliation/validation of invoices;
  
  tracking of spend vs budget).
• Manage and track CMO performance prior to (preparation), during (direct oversight) and after (campaign summaries/reports) manufacturing.
• Manage and track batch data in compliant (data‑integrity) systems to support filing submissions, patient planning and process optimization.
• Work closely with CMO and internal Quality and Technical teams to prioritize, monitor, track, review and deliver required compliance documentation (including but not limited to change controls, investigations and deviations, batch data, CAPA effectiveness, internal/external audit observation deadlines, regulatory commitments) to meet Vertex program requirements.
• Identify and elevate business‑critical issues to Commercial Manufacturing and Supply Chain, CMC, and Quality leadership.
• Collaborate with CMO and internal stakeholders to understand planned changes and manage the end‑to‑end implementation of agreed changes including but not limited to change controls and impact assessments.
• Lead continuous improvement initiatives to affect timely resolution of…