Overview
Our Company's Vaccines Technical Leadership team within the Global Science and Technology (GSEC) organization is seeking a Director to lead the Pneumococcal Vaccines (PCV) - Development and Commercial Team Leadership (DCT) and the technical product leads.
The role provides end-to-end technical product leadership and strategic direction for PCV vaccine products across their lifecycle-from development through commercialization and sustained supply.
The Director will lead a team of specialists and collaborate across multiple functions and global manufacturing sites to ensure robust, compliant, and innovative manufacturing science and technology solutions.
Responsibilities
Serve as the primary technical leader for the PCV franchise, owning the product's technical processes and challenges, proactively managing risks, and driving innovative solutions aligned with business goals.
Lead the Development and Commercial Team (DCT), accountable to Development Commercialization Review Committee (DCRC) for delivering a fully integrated stage-appropriate development and commercialization strategy for PCV products.
Critically assess all team deliverables, foster a learning and collaborative environment, prioritize and mitigate risks across technical, operational, and regulatory domains, and develop innovative solutions for unforeseen circumstances.
Provide strategic technical leadership and project execution for strategic and supply initiatives, partnering with manufacturing sites globally.
Be responsible for end-to-end technical product leadership and oversight of on-time deliverables including robust processes and analytics, an integrated control strategy, successful tech transfer packages, filings and approvals, and a robust commercial supply chain for launch on time and uninterrupted supply.
Collaborate with Research Laboratories, Process Development, Commercialization, Operations, Quality, Regulatory-CMC, and Supply Chain teams to ensure seamless technology transfers, process validation, regulatory filings, and product launches.
Ensure process and assay robustness through continuous monitoring, risk identification, and rapid resolution of technical issues within the manufacturing network.
Represent CMC interests in governance bodies, influencing cross-functional strategies to balance speed, cost, and robustness for successful product launch and long-term supply.
Develop and implement Knowledge Management strategies to support regulatory filings and lifecycle management of technical product information.
Provide on-site technical support for critical projects, complex investigations, and specialized requests at manufacturing sites.
Foster strong, trusting relationships with site leaders, functional management, and stakeholders to ensure effective communication and alignment.
Drive a culture of safety, compliance, integrity, and inclusion in all activities.
Core Competencies
Development & Commercialization Expertise:
Understanding of technical interdependencies across Drug Substance, Drug Product, Device, Packaging, Analytical, Regulatory, Quality, and Supply Chain from early development through commercial manufacturing.
Technical Leadership:
Recognized scientific leadership with the ability to navigate uncertainty and deliver favorable outcomes.
Strategic Thinking:
Ability to see the "big picture," ask critical questions, and drive decisions that balance enterprise priorities.
Problem Solving & Innovation:
Skilled in analyzing complex data, fostering debate, and developing creative solutions to technical challenges.
Ambiguity Navigation:
Comfortable operating in uncertain environments, adapting plans, and making disciplined risk-based decisions.
Communication:
Effective at leading complex discussions, influencing stakeholders, and tailoring messages to diverse audiences.
Collaboration & Teamwork:
Builds and leads high-performing teams, promotes open communication, and fosters inclusive environments.
Results Orientation:
Drives accountability and ensures on-time delivery of projects and commitments.
Influence & Ownership:
Inspires action, builds trust, and demonstrates initiative to see challenges through to completion.
Compliance & Culture
Adhere to our company's global and regulatory requirements and current Good Manufacturing Practices (cGMP).
Promote a safe, compliant, and inclusive culture within the organization and teams.
Education & Experience
Bachelor of Science (BS) in Biological Sciences, Chemical Engineering, Biochemical Engineering, Bioengineering, or related field with twelve (12) years of experience; OR
Master of Science (MS) in Biological Sciences, Chemical Engineering, Biochemical Engineering, Bioengineering, or related field with ten (10) years of experience; OR
Ph.D. in Biological Sciences, Chemical Engineering, Biochemical Engineering, Bioengineering, or related field with seven (7) years of relevant experience.
Experience & Skills
Extensive experience in vaccine, biologics, or pharmaceutical industries.
Strong scientific understanding of vaccine/biologic products and processes integrated with regulatory and GMP requirements.
Proficiency in technical business processes including Change Control, Deviation Management, and Technical Protocols/Reports.
Demonstrated problem-solving, communication, and interpersonal skills.
Preferred Experience & Skills
Experience in pneumococcal vaccine manufacturing or development.
Experience authoring BLA/MAA regulatory license documents.
Knowledge of vaccine/chemistry processes (fermentation, purification, formulation, filling, packaging).
Familiarity with regulatory requirements for vaccine and biologics manufacturing.
Experience with DMAIC / Lean Six Sigma or equivalent methodologies.
Additional Information
Current Employees apply HERE
Current Contingent Workers apply HERE
US and Puerto Rico Residents Only: accommodation information available on request.
EEOC statements and rights information are provided as part of the posting; see details for more information.
Travel: 10%; Hybrid work model in the U.S. with three on-site days per week; some roles require on-site presence per business needs.
Salary range: $169, $267,200.00; eligibility for annual bonus and long-term incentive, if applicable.
Application: You can apply for this role through (or via the Workday Jobs Hub if you are a current employee).
The application deadline is listed in the posting.