Executive Director, Small Molecule CMC Lead

BeOne Medicines Ltd.; Pennington (NJ); Presencial; USD 180 000 - 260 000; Tempo integral

Resumo da oferta

BeOne Medicines Ltd. seeks a CMC Lead to drive development strategy and execution for assigned programs from clinical through regulatory submission and commercialization.

You will be the single accountable point for CMC program governance, aligning development, manufacturing readiness, regulatory expectations, quality standards, and business goals. You will lead cross-functional teams, manage external CDMOs, identify risks, and ensure robust, scalable GMP‑compliant drug substance and drug

Qualificações

• Ph.D. or equivalent degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Biochemistry, or related discipline preferred.
• Advanced degree (MS/PharmD) with extensive pharmaceutical industry experience may be considered.
• 8+ years of pharmaceutical/biotechnology industry experience in CMC development.
• Experience leading CMC activities for NCE through clinical development and regulatory approval.
• Experience supporting IND/NDA submissions.
• Strong understanding of CMC development, GMP manufacturing, and regulatory CMC expectations.
• Proven ability to lead cross-functional teams without direct authority.
• Strong strategic thinking and problem-solving capability.

Responsabilidades

• Develop and execute comprehensive CMC strategies aligned with development objectives and corporate goals.
• Lead CMC planning and execution across development stages, including clinical development and regulatory submissions.
• Define CMC milestones, deliverables, timelines, resources, and risk mitigation.
• Provide strategic oversight of drug substance and drug product development activities for GMP manufacturing.
• Ensure analytical strategies support regulatory submissions and lifecycle management.
• Partner with Regulatory Affairs to develop CMC regulatory strategies and responses.
• Establish governance for CMC decision-making and lead trade-off analyses.
• Identify CMC risks and implement mitigation plans throughout development.
• Manage CDMOs and external vendors to meet scope, timelines, and budgets.
• Support transition to commercial manufacturing and readiness for PPQ and inspections.

Conhecimentos

CMC leadership

Strategic thinking

Cross-functional leadership

Regulatory liaison

Data-driven decision making

Communication skills

Risk management

Project management

Formação académica

Ph.D. in Pharmaceutical Sciences

MS/PharmD consideration

Descrição da oferta de emprego

The CMC Lead is a strategic and cross‑functional leader responsible for driving the CMC development strategy and execution for assigned drug programs from clinical development through regulatory submission, approval, and commercialization. The CMC Lead serves as the single point of accountability for CMC program strategy, ensuring alignment of technical development, manufacturing readiness, regulatory requirements, quality expectations, and business objectives.

The successful candidate will provide strong scientific and operational leadership, integrate internal and external CMC capabilities, proactively identify technical risks, and enable efficient delivery of high‑quality drug substance and drug product to support clinical and commercial success.

Key Responsibilities

• Develop and execute comprehensive CMC strategies aligned with overall development objectives and corporate goals.

• Lead CMC planning and execution across development stages, including pivotal clinical development, registration submission, commercial manufacturing readiness, post‑approval lifecycle management.

• Define critical CMC milestones, deliverables, timelines, resource needs, and risk mitigation strategies.

• Provide strategic oversight of drug substance and drug product development activities. Ensure processes are scientifically sound, robust, scalable, and suitable for GMP manufacturing. Partner with CDMOs and manufacturing sites to ensure successful execution of clinical and commercial supply.

• Ensure appropriate analytical strategies are established to support product development and regulatory requirements. Ensure analytical packages support regulatory submissions and lifecycle management.

• Partner with Regulatory Affairs to develop high‑quality CMC regulatory strategies. Support preparation of regulatory briefing packages, responses to agency questions, and commitments.

• Establish effective governance mechanisms for CMC decision‑making. Lead technical assessments and trade‑off decisions balancing quality, speed, cost, regulatory expectations, and long‑term commercial needs.

• Identify CMC risks and establish mitigation plans throughout development.

• Provide strategic oversight of CDMOs and external vendors. Ensure external partners deliver against agreed scope, timelines, quality standards, and budgets. Lead escalation management when needed.

• Support transition from development to commercial manufacturing. Ensure CMC readiness for PPQ campaigns, Regulatory submission/inspections, launch supply, and post‑approval changes.

• Develop lifecycle strategies to improve product robustness, cost, capacity, and supply reliability.

• Serve as the primary CMC representative on cross‑functional development teams.

• Lead collaboration among all CMC technical functions, commercial manufacturing, QA/QC, regulatory CMC, clinical development, supply chain, external CDMO partners, etc.

• Ensure effective communication, alignment, and decision‑making across functions.

• Drive resolution of complex technical and operational challenges.

Required Qualifications

• Ph.D. or equivalent degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Biochemistry, or related discipline preferred.

• Advanced degree (MS/PharmD) with extensive pharmaceutical industry experience may be considered.

• 8+ years of pharmaceutical/biotechnology industry experience in CMC development.

• Demonstrated experience leading CMC activities for NCE through clinical development and regulatory approval.

• Experience supporting successful IND and NDA submissions.

• Strong understanding of CMC development, GMP manufacturing, and regulatory CMC expectations.

• Proven ability to lead cross‑functional teams without direct authority.

• Strong strategic thinking and problem‑solving capability.

• Ability to make data‑driven decisions under uncertainty.

• Excellent communication skills with technical, executive, and regulatory stakeholders.

Preferred Qualifications

• Experience leading multiple pipeline programs simultaneously.

• Experience managing both internal and outsourced development/manufacturing models.

• Experience with global regulatory agencies (FDA, EMA, NMPA).

• Experience with commercialization, technology transfer, PPQ, and post‑approval lifecycle management.

• Experience building CMC organizations or implementing CMC governance models.

Key Success Metrics

• Delivery of CMC milestones according to program timelines.

• Successful IND/NDA submissions and regulatory interactions.

• Robust clinical and commercial supply readiness.

• Effective management of CMC risks and external partners.

• Strong collaboration across development functions.

• Development of scalable, cost‑effective, and compliant manufacturing processes.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.