Sr Director, BSMO Disease Area Lead — Immunology Disease Strategy Team

Job Description

General Summary

The Senior Director, BSMO Immunology Disease Area Lead represents BSMO on the Immunology Disease Strategy Team (DST). The incumbent provides strategic and operational leadership for all BSMO activities supporting programs across the Immunology portfolio, and is accountable for driving an integrated BSMO program strategy, alignment, and execution across Pharmaceutical Sciences, Biopharmaceutical Sciences, CMTO, Quality, Supply Chain, Regulatory, Finance, and other relevant functions to support development, launch, and lifecycle management of disease-area products. As a core member of the Immunology DST, this leader partners cross-functionally to translate disease strategy into executable technical and operational plans that enable reliable, compliant delivery of biologic medicines to patients with serious immune-mediated disease. By sitting on the DST, this role ensures BSMO priorities and resources are aligned with the broader disease-area strategy, that BSMO has visibility to disease-area developments, and that the DST understands BSMO activities and capabilities.

Key Duties and Responsibilities

• Lead the development and execution of the BSMO program strategy for Immunology programs, aligned with disease, clinical, and commercial strategies.

• Serve as the BSMO representative on the Immunology DST, supporting governance, planning, and risk discussions.

• Provide integrated leadership across Pharmaceutical Sciences, Biopharmaceutical Sciences, CMTO, Quality, Supply Chain, and external partners to ensure program readiness.

• Partner cross-functionally within BSMO to integrate plans to develop and commercialize biologic disease-area products, ensuring regulatory compliance.

• Support biologics CMC regulatory strategy and submissions in partnership with Regulatory, including IND/IMPD and BLA/MAA content and health-authority interactions as needed.

• Lead cross-functional BSMO teams to deliver against program milestones in a matrixed environment, requiring a robust understanding of each BSMO function's role.

• Build effective partnerships with internal stakeholders within BSMO and more broadly across the enterprise.

• Identify and manage program-level technical, operational, and supply risks for biologic products, ensuring appropriate escalation and mitigation planning.

• Own BSMO program budgets, forecasts, and resource plans, aligning with functional and DST priorities (AOP/LRP).

• Track and communicate program status, KPIs, and risks to BSMO and DST leadership.

Required Knowledge and Skills: (biologics-weighted)

• Strong expertise in biologics development and manufacturing across the lifecycle, including cell-line/upstream cell culture, downstream purification, drug substance, formulation, drug product/fill-finish, and device/combination-product considerations where applicable.

• Working command of biologics CMC fundamentals: process and analytical development, control strategy, product and process characterization, comparability and change management , and process validation/PPQ.

• Understanding of biologics-specific technical risks — product/process sensitivity, aggregation and immunogenicity, glycosylation and other critical quality attributes, stability, and cold-chain requirements.

• Solid understanding of CMC, Quality/GMP, Regulatory, and Supply Chain requirements for biologic products, including inspection readiness.

• Experience with external manufacturing / CDMO oversight for biologic drug substance and drug product, including technology transfer and scale-up.

• Capability to build cross-functional alignment across R&D, Pharmaceutical/Biopharmaceutical Sciences, Regulatory, Finance, Commercial, and Manufacturing partners.

• Demonstrated expertise in critical thinking, influence, negotiation, problem-solving, strategic thinking, and leadership in a matrix environment; proven ability to influence areas not under direct control.

• Excellent verbal, written, and presentation skills.

Education and Experience

• Advanced degree in a relevant scientific or engineering discipline (e.g., Biochemistry, Biology/Immunology, Chemical or Biochemical Engineering, Pharmaceutical Sciences); PhD and/or MBA preferred .

• 12 years of experience, or equivalent, in biopharmaceutical development, manufacturing, and supply chain, with substantial hands-on biologics experience .

• Demonstrated experience leading cross-functional program teams and advancing products through one or more development stages.

At Vertex, we embrace continuous learning and encourage employees to stay informed on advances in AI, technology, automation, and industry trends. We seek talent who bring an external perspective, demonstrate curiosity and sound judgment, and thoughtfully adopt new capabilities that improve decision-making, drive innovation, increase efficiency, and help deliver better outcomes for patients.

Pay Range

$218,400 - $327,600

Disclosure Statement

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.  From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

Flex Designation

Hybrid-Eligible Or On-Site Eligible

Flex Eligibility Status

In this Hybrid-Eligible role, you can choose to be designated as:

1.     Hybrid : work remotely up to two days per week; or select

2.     On-Site : work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex Vertex Program and may be changed at any time.

#LI-Hybrid

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance vrtx.com