Molecule Steward

Position Summary

This is a truly exciting opportunity for an experienced scientific professional to take end-to-end technical accountability for a given product, from bulk API manufacturing, formulation, packing and related support activities, providing strategic technical leadership to ensure successful new product introduction, quality robustness and productivity improvements across the lifecycle.

The Molecule Steward is aligned to a new asset at Commit to Commercial Development with responsibility for representing MSAT in the development of the Product Control Strategy.

When the product transfers to GSC accountability, the Molecule Steward co‑ordinates Drug Substance, Drug Product, Analytical Strategy and, if appropriate, Device Leads to maintain the Product Control Strategy and ensure the product is maintained in the desired state of control throughout the product lifecycle.

You will be responsible for developing and delivering the technical elements of the Global Supply Chain strategy with the GSC Strategy Lead and will be a recognised GSC expert in the given product or dose form.

In addition to strategic technical leadership, the role will be expected to provide deep technical expertise where required to ensure highest levels of quality and robustness.

Responsibilities

• Represent MSAT as technical single‑point accountable decision maker to CMC Matrix and Medicine Supply Chain teams, ensuring that a product control strategy is defined and maintained to drive a robust product that meets target manufacturability criteria.
• Define the End‑to‑End Product Performance Qualification and Ongoing Continuous Verification Strategy for the product, including trending and sampling plans and ensuring alignment and consistency across supply nodes.
• Maintain accountability for the product, from transfer from R&D throughout its lifecycle, ensuring improvement plans (including 2nd generation processes) are developed and delivered impacting the manufacturing process, analytical process, pack, device, and associated specifications to deliver value.
• Maintain solid knowledge and understanding of complex scientific subject matter as well as evolving regulatory policies and guidelines and industry best practices, using this knowledge to develop improvement plans for the products.
• Act as accountable MSAT perspective for defining technology strategy and specific solutions as required to support the overall product or dose form lifecycle.
• Lead Product Technical Lifecycle Teams, ensuring risks are identified and mitigated and technical issues are resolved in a timely manner.
• Coordinate review of regulatory submissions and responses to technical questions within MSAT, ensuring review by appropriate SMEs and sites.
• Provide leadership and subject matter expertise for investigations and/or critical deviations, troubleshooting, and major change programs.
• Ensure that product history and knowledge from development through lifecycle is maintained and aligns with knowledge management standards for the product or dose form within the GSC network.
• Manage strong collaborations with technical staff across the Supply Chain sites, MSAT & R&D, with effective and clear communication on highly technical topics.

Must be able to lead and operate in an environment with a high degree of change and uncertainty.

• Basic Qualifications
• University Degree (minimum) in Chemistry, Chemical engineering, Pharmaceutical Sciences or similar area.
• Extensive years’ experience in small molecule pharmaceutical development and/or manufacturing.
• Comprehensive knowledge of external regulatory requirements (MHRA, FDA), and internal/external quality and safety requirements.
• Experience in technology transfer, with an understanding of the product development process.
• Knowledge of current and emerging Regulatory Strategies (Quality by Design, GMP for 21st century, ICH Q7, Q8, Q9, Q10) and Product Lifecycle Management.
• Demonstrated experience in the pharmaceutical industry in leading the technical aspects of Product Lifecycle Management, including supporting process investigations.
• Preferred Qualifications
• Project management and prioritization skills gained within a complex matrix.
• Excellent problem solver and ability to think and work creatively.
• Strong technical acumen and communication skills with the ability to articulate complex, technical details to stakeholders and enable cross‑functional collaboration across sites, supply chain, R&D, and suppliers.
• Experience managing external partners/CDMOs in NPI and/or commercial supply.
• Ability to effectively influence stakeholders at all levels.
• Work Location

This role can be based in Ware, Worthing, Barnard Castle, UK; or Upper Providence or Durham, USA and offers a hybrid working model, combining on‑site and remote work.

Skills

CMC Strategy, Data‑Driven Decision Making, Data Integrity, Debate Moderation, Digital Fluency, Gx P Regulations, Lean Management, Problem Solving, Process Optimization, Project Leadership, Risk Awareness, Scientific Writing, Technology Transfer.

Benefits

Benefits include a comprehensive benefits program for U. S. employees.

Equal Opportunity Employer

GSK is an Equal Opportunity Employer.

This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

Accommodations for Applicants

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at

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