Director, Global Drug Substance Commercialization, Polysaccharide

Vaxcyte; United States; Remote; USD 223,000 - 261,000; Full time

Benefits offered by this job

Equity component

Comprehensive benefits

Job summary

Vaxcyte, a clinical-stage vaccine company in the United States, seeks a Director for Drug Substance Commercialization of Polysaccharides to lead technical launch planning and cross-functional execution. You will coordinate regulatory filings, facility readiness, and launch supplies while guiding lifecycle management for polysaccharide processes.

The role requires experience in biologics manufacturing, strong leadership, and the ability to communicate scientific and commercial rationales to

Qualifications

• 10+ years in MSAT or Process Development for PhD level, or 12+ for MS, 16+ for BS.
• Experience with biologic production and polysaccharides preferred.
• Leadership experience in cross-functional, matrixed teams.
• Ability to translate strategy into executable programs.
• Strong organizational, planning, and communication skills.

Responsibilities

• Lead polysaccharide commercialization programs and cross-functional workstreams.
• Coordinate regulatory, CMC, Quality, and Supply Chain deliverables.
• Drive tech-transfer and adoption of new technologies across sites.
• Provide technical oversight of CMOs and lifecycle planning.
• Communicate process performance and strategic rationale to stakeholders.

Skills

Strategic leadership

Cross-functional coordination

Regulatory understanding

Communication skills

Problem solving

Project management

Data-driven decision making

Education

PhD in Chemical/Biochemical Eng

MS in Chemistry/Biochemistry

BS in related field

Job description

Join our Mission to Protect Humankind!

Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.

WHAT we do is every bit as important as HOW we do it!Our work together is guided by four enduring core values:

*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.

*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.

*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.

*MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.

Summary:

The Director for Drug Substance Commercialization of Polysaccharides will lead assigned commercialization workstreams and facilitate overall launch readiness and commercial supply of the polysaccharides used in glycoconjugate vaccines.

This role focuses on technical launch planning and execution by bringing best-practices and coordinating cross-functional efforts for regulatory filings, facility readiness, and launch supplies.

This role also provides leadership to ensure that the organization is equipped to effectively communicate the scientific and commercial rationale for critical raw material manufacturing processes to internal stakeholders, relevant CMOs, and to regulatory agencies. The incumbent will work with the organization to ensure on-time execution and appropriate planning for commercial lifecycle management.

This position will be reporting into the Senior Director for Global Polysaccharide Commercialization. The Director will collaborate on overall program strategy, with primary responsibility and accountability for the Polysaccharide component strategy.

Manufacturing Science and Technology (MSAT) is responsible for successfully and seamlessly transitioning the vaccine process from Process Development to Commercial, developing and executing technical launch and commercialization strategy, continuously improving process robustness through to end of lifecycle, and ensuring best possible patient outcomes while creating value for the enterprise. As part of the Commercial Manufacturing and Supply Chain organization, MSAT will lead the technical and process support for end-to-end commercial manufacturing, including Polysaccharides, Carrier Proteins, and Conjugation across all Drug Substances (DS). The range of activities will include technology transfer support, process characterization experiments in support of validation, process improvement, evaluation of novel process technologies, investigation of process related manufacturing issues, ensuring continuous improvement in process robustness throughout the product life cycle, etc.

Essential Functions:

• DS Commercialization – Provide strategic and scientific leadership for polysaccharides with internal and external stakeholders and ensure successful execution of launch plans and post-launch commercial activities by translating strategy into execution plans and ensuring completion of key technical milestones.
• Organization and capability building – Develop technical capabilities within the polysaccharide commercialization organization and support resource and staffing recommendations needed to achieve program and organizational objectives. Contribute to building a highly skilled team capable of supporting the global manufacturing network.
• Process robustness – Continuously improve process understanding and process robustness using staff and laboratory resources across the organization to monitor, trend, and optimize operations.
• Interface – Coordinate cross-functional deliverables across the network, including Regulatory, CMC, Quality, Supply Chain, Procurement, and Process Engineering, to drive the successful development and commercial launch of polysaccharides for pipeline products. Identify, communicate, and investigate technical and supply risks that may impact program execution or commercial supply.
• Tech-transfer and new technologies – Ensure robust processes exist to support technical transfers and integration of new technologies, providing technical oversight to support successful execution across internal and external manufacturing sites.
• Support technical services – Support our internal and external manufacturing network, including materials management and data analytics, and provide technical oversight of CMOs to support reliable manufacturing and commercial supply.
• Process validation and comparability – Provide leadership for the execution of process validation and process comparability activities. Effectively communicate the scientific and commercial rationale for polysaccharide processes to the Manufacturing organization for commercialization.
• Regulatory – Engage in technical review and authoring of regulatory filings and respond to questions received from health authorities. Effectively communicate the scientific and commercial rationale for polysaccharide processes to Boards of Health for regulatory submissions supporting commercialization.
• Communicate – Effectively and efficiently communicate process performance to key stakeholders, both internal and external. Connect and build strong working relationships with others, demonstrating strong emotional intelligence and an ability to communicate clearly and persuasively.
• Leadership – Lead assigned polysaccharide commercialization programs and technical workstreams** ,** coordinating execution across stakeholders and contributing as a member of the Global Manufacturing Operations organization, with an aim to ensure effective and efficient delivery of our life-enhancing therapies to our patients.
• Travel - 10-30% travel required.

Requirements:

• Degree(s) in Chemical or Biochemical Engineering, Chemistry, Biochemistry, or related discipline with a minimum of 10+ years of relevant experience for Ph.D., 12+ years for M.S./M.A., or 16+ years for B.S./B.A.
• Extensive experience in biologic production processes, including bacterial fermentation, recovery, and purification across multiple operational scales. Experience with polysaccharides and glycoconjugate vaccines highly preferred.
• Leadership experience in MSAT or Process Development in supervisory and/or matrixed team roles.
• Able to leverage deep technical knowledge in a collaborative manner to establish strategic plans and achieve collective goals.
• Excellent organization, problem solving and strategic planning skills.
• Highly skilled in both verbal and written communication with the ability to interact effectively with people of diverse backgrounds and perspectives.
• Proactively recognizes needs and potential challenges, and directs activities to implement effective solutions.
• The ability to seek and analyze data from a variety of sources to support decisions and to align others with the organization’s overall strategy.
• An entrepreneurial and creative approach to developing new, innovative ideas that will stretch the organization and push the boundaries within the industry.

Reports to: Senior Director, Global Polysaccharide Commercialization Lead

Location: United States

Work Arrangement (may be adjusted based on business needs, job responsibilities, or changes to company policy):

Remote

Compensation:

The compensation package will be competitive and includes comprehensive benefits and an equity component.

Salary Range: $223,000 - $261,000 (SF Bay Area). Salary ranges for non-California locations may vary.

Relocation:

This role is not eligible for relocation assistance.

Equal Opportunity

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.