Quick Overview
Job Description
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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 escalate 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.
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.
Recruitment Fraud Notice
Please be aware of fraud or scams from individuals, organizations and/or internet sites claiming to represent Vaxcyte in recruitment activities. Vaxcyte has an established recruitment process for all positions prior to issuing an offer for employment and we will never extend unsolicited employment offers or ask candidates to provide financial or sensitive personal information as part of the application process. All legitimate communication from Vaxcyte will come from an official @vaxcyte.com email address. Qualified and interested candidates should apply to current openings at vaxcyte.com/careers.
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