GSK
Biopharma
MoleculeSteward
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Molecule Steward at GSK. Skills: Product Control Strategy, Product Lifecycle Management, Technical Leadership, Scientific Expertise. Represent MSAT as technical single-point accountable decision maker. Define End-to-End Product Performance Qualification”
What You'll Achieve.
Ensure successful new product introduction; Ensure quality robustness; Ensure productivity improvements; Ensure product is maintained in desired state of control; Deliver value; Mitigate risks; Resolve technical issues; Align with knowledge management standards
Industry & Context.
Problem solver; Technical issues resolved
What They're Looking For.
Must Have
University Degree (minimum) in Chemistry, Chemical engineering, Pharmaceutical Sciences or similar area, Extensive years’ experience in pharmaceutical development and/or manufacturing, ideally in small molecule modality, Comprehensive knowledge of external regulatory requirements (MHRA, FDA), and internal/external quality and safety requirements, Experienced 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.
Nice to Have
Project management and prioritization skills gained within a complex matrix, Excellent problem solver and ability to think and work creatively, 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/CDMO’s in NPI and/or commercial supply, Ability to effectively influence stakeholders at all levels
What You'll Do.
Represent MSAT as technical single-point accountable decision maker
Define End-to-End Product Performance Qualification
Define Ongoing Continuous Verification Strategy
Maintain accountability for product lifecycle
Develop and deliver improvement plans
Define technology strategy & specific solutions
Lead Product Technical Lifecycle Teams
Coordinate review of regulatory submissions
Provide leadership for investigations
Ensure product history and knowledge is maintained
How You'll Work.
Team & Collaboration
Collaborate with technical staff across Supply Chain sites, MSAT & R&D; Enable cross functional collaboration across sites, supply chain, R&D and suppliers
Communication Scope
Communication skills; Articulate complex, technical details; Clear communication on highly technical topics
Process & Methodology
Project management, Prioritization skills
Full Job Description
# **Molecule Steward** **Business Introduction** We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients. **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 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
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