At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim to prevent stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche where every voice matters.

The Position

Roche Pharma Global Technical Operations (PT) delivers a fast evolving portfolio of new Cell & Gene Therapy (CGT) products to bring new curative treatments to patients. This portfolio of new products comes with the great promise to bring unprecedented medical advances to patients but also presents unique challenges as the Regulatory landscape is evolving very quickly.

The opportunity

The Value Chain Product Lead (VCPL) in Cell and Gene Therapy holds end-to-end (E2E) Value Chain ownership for specific CGT products. This is a crucial matrix leadership role accountable for ensuring products achieve E2E Value Chain readiness for upcoming clinical trials and/or commercial launches. The specific responsibilities will adapt based on the products phase (early/late clinical commercial launch) partnership structures and targeted timelines.

Key Attributes & Collaboration

• Thrives in ambiguous fast-paced environments demonstrating strong learning agility excellent communication and stakeholder management skills.

• Collaborates closely with cross-functional teams (Technical Development Clinical Commercial GPS) and external CDMOs; contributes to new system/process development.

Core Responsibilities

• Leads and manages E2E Value Chain product teams (OEM Patient Ops Supply Chain) overseeing schedules risk logs and ensuring operational delivery aligned with CMC Roadmaps and TDT/TPT commitments.

• Manages supply chain planning across all product lifecycle phases driving effective stakeholder management (PTC/Commercial) and partnering with E2E VC Capability Leads.

• Orchestrates day-to-day operational activities for flawless E2E value chain execution supporting patient treatment.

Key Responsibilities & Job Requirements

• Owns comprehensive product plans and forecasts (OEM Patient Ops Supply Chain/Logistics) to ensure delivery across CMC Clinical and Commercial timelines; leads commercial S&OP.

• Manages daily manufacturing partner interactions for personalized therapy delivery (scheduling capacity allocation); acts as key decision-maker for product risks collaborating with Capability/VC Strategy Leads and CSCL for comparator supply.

• Defines key processes (e.g. ordering slot management) and provides user requirements for E2E capabilities (e.g. ATHEROS CoC/CoI); leverages ERP experience for system design.

• As a Technical Development Team member brings Value Chain risks/opportunities to SMEs (Regulatory Formulations Process Engineering Quality); coordinates label design/compliance and new product/country configurations with Master Data Management.

• Coaches colleagues and leads complex products (late-stage multiple trials) driving proactive strategy and direction.

Who you are

Were looking for a highly adaptable individual who thrives in a continuously evolving and often ambiguous environment. Youll be a team player excited to take on a range of responsibilities from tactical roles to strategy projects. Youll also possess excellent verbal and written communication skills with a proven ability to succinctly share information and influence decisions across all levels. The ideal candidate will demonstrate effective collaboration skills working seamlessly within highly matrixed cross-functional teams and with external partners. Youll also need the ability to work effectively in a dynamic fast-paced environment and adeptly manage change readily embracing new challenges and shifting priorities.

Furthermore you bring the below qualifications and experience:

• Masters or Bachelors degree in management engineering and/or sciences and/or supply chain is preferred.

• 12 years (10 years with Masters) of work experience in matrix leadership clinical trial set-up supply chain planning and supporting systems (eg. SAP scheduling MRP CGT Orchestration etc.) in either a clinical or commercial environment.

• Experience with cell and gene therapy supply chain design and management in the pharmaceutical/biotech industry is a plus.

• Experience with successfully leading complex cross-functional projects which demonstrated an ability to think creatively and drive for results.

This position requires 10-20% domestic and international travel and is based out of South San Francisco and/or Basel. Plan for hybrid working (part in person and remote every week). Expectation to be in person for key workshops and meetings. Global hours are expected (7am-9am PT/ 4-6pm CET).

Who we are

A healthier future drives us to innovate. Together more than 100000 employees across the globe are dedicated to advance science ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities foster creativity and keep our ambitions high so we can deliver life-changing healthcare solutions that make a global impact.

Lets build a healthier future together.