MSAT 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(s), 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 molecule 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 Global Supply Chain (GSC) accountability, the Molecule Steward co-ordinates Drug Substance, Drug Product, Analytical and if appropriate Device technical strategy to ensure the product is maintained in the desired state of control throughout product lifecycle and meets business and scientific objectives.

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.

• Representing 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 and quality elements.

• Responsible for defining the End-to-End Product Performance Qualification and ongoing Continuous Process Verification strategy for the product, including trending and sampling plans and ensuring alignment and consistency across supply nodes.

• Maintaining accountability for the product, from transfer from R&D throughout its lifecycle, ensuring robust continuous improvement plans and technical roadmap (including 2nd generation processes) are developed and delivered improving the manufacturing process, analytical process, pack, device, and associated specifications to maximize the value of the asset(s).

• Maintaining solid knowledge and understanding of complex scientific subject matter as well as evolving regulatory policies and guidelines and industry best practices.

• Accountable for defining technology strategy & specific solutions as required to support the overall product or dose form lifecycle.

• Responsible for leading Product Technical Lifecycle Teams (PTLT), ensuring risks are identified and mitigated whilst driving continuous improvement of the technical aspects of the molecule and associated processes.

• Responsible for co-ordinating the review of regulatory submissions and responses to technical questions within MSAT.

• Providing leadership and subject matter expertise where required for investigations and/or critical deviations,troubleshooting, and major change programmes. Driving matrixed leadership to ensure technical issues are resolved in a timely manner.

• Ensuring 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.

• Managing strong collaborations across the Supply Chain sites, MSAT & R&D, with effective and clear communication on highly technical topics to all levels of the organization.

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

• University Degree (minimum) in Life Sciences (e.g. Biology, Chemistry,etc.) 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.

• Direct experience with complex pharmaceutical devices and delivery systems; specific experience with inhalation devices highly desired.

• Project management and prioritization skills gained within a complex matrix

• Excellent problem solver and ability to think and work creatively

• Strong communication skills with the ability to articulate complex, technical details to matrixed team at all levels of the organization.

• Ability to effectively influence stakeholders at all levels

Work Location:

This role can be based in Ware, London, Barnard Castle, UK, Evreux, France or Upper Merion, Upper Providence, Boston, or Durham, USA and offers a hybrid working model, combining on-site and remote work.

Closing Date for Applications: 24th July 2026

Please take a copy of the Job Description, as this will not be available post closure of the advert.When applying for this role, please use the 'cover letter' of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.

#Li-Hybrid

If you are interested, please apply and tell us how your experience aligns with the basic qualifications and responsibilities above. We look forward to learning how you would contribute to safe, robust supply and lasting patient impact.

Skills

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

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.

We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at UKRecruitment.Adjustments@gsk.com where you can also request a call.

Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/