Associate Principal Scientist, Engineering - Vaccine, Sterile Drug Product Commercialization

Job Description Position Description Associate Principal Scientist, Vaccine, Sterile Drug Product Commercialization

As part of Our Company's Manufacturing Division, the Sterile Drug Product Commercialization group provides the technical process leadership and laboratory capabilities for late stage and commercial drug product processes for vaccines, biologics, and sterile pharmaceutical products.

It is the division's leader in sterile product and process development, responsible for late-stage commercialization activities including process scale up, technology transfer to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The group is responsible for establishing the science, engineering and knowledge required for today's innovative and accelerated commercialization of novel vaccines, biologics, and pharmaceutical products and combination products.

We are seeking an experienced Associate Principal Scientist to advance and commercialize biologics pipeline program. As a member of the biologics drug product team, the Associate Principal Scientist will have a key focus on driving excellence in process characterization, scale up, transfer and process validation activities.

• Leads and/or serves on cross functional Vaccine drug product (DP) working groups to support early and late pipeline programs.
• Partner with early development vaccine program teams to ensures that commercial product definition and process definitions align with manufacturing capabilities and robustness objectives
• Leads DP activities through filing and Process Performance Qualification (PPQ), including registration stability study execution, process characterization plan and execution, tech transfer control strategy, process development, PPQ readiness, PAI (Pre-Approval Inspection) readiness, approval, launch and post-launch support.
• Drives strategic initiatives (technical and/or business process related) with partner groups, that enable more efficient and rapid commercialization of innovative products
• Provides mentorship, technical oversight and strategic guidance to employees. Uses advanced experience gained on scientific/technical issues to guide others to address non routine and/or difficult issues.
• Design and execution of DP development and commercialization studies, new product introduction and process validation at commercial sites.
• Ensures fit-for-purpose scale-down models are developed and employed. Establishes and validates platform engineering and scientific models for sterile product and process commercialization.
• Influences CMC regulatory strategy and is accountable for DP CMC sections of filing. Reviews regulatory strategy and filing readiness and supports preparations for agency meetings. Authors and reviews regulatory submissions.
• Drives continuous and phase appropriate process optimization towards standardized platforms for liquid, lyophilized, and combination product presentations.
• Establishes and fosters a culture of high performance, out of the box thinking, innovation and learning, empowerment, diversity and inclusion.

This position may require travel up to 25%;
Must be able to travel for this position.

• B.S. in Chemical Engineering, Biochemical Engineering
  - Bio-engineering, Pharmaceuticals, Biochemistry, Microbiology, or related field with 10 years of relevant experience; or
• Master's degree in Chemical Engineering, Biochemical Engineering
  - Bio-engineering, Pharmaceuticals, Biochemistry, Microbiology, or related field with 8 years of relevant experience; or
• Ph.D. in Chemical Engineering, Biochemical Engineering
  - Bio-engineering, Pharmaceuticals, Biochemistry, Microbiology, or related field with 4 years of relevant experience

• Experience with drug product process development, optimization, and/or process characterization of vaccines modalities such as conjugates, LVV, VLP, subunit, adjuvants)
• Working understanding analytical methods to characterize vaccines
• Understanding of knowledge of current Good Manufacturing Practices (cGMPs) for manufacturing sterile dosage forms and current ICH Quality norms, as applied in Manufacturing Science and Technology or Technical Operations.
• Understanding of regulatory requirements for commercialization and registration of sterile drug products,…