At a Glance
- Tasks: Lead technical strategy for innovative medicines and vaccines, ensuring quality and efficiency.
- Company: Join a global biopharma leader dedicated to improving health for billions.
- Benefits: Competitive salary, hybrid work model, and opportunities for professional growth.
- Other info: Dynamic work environment with strong career advancement potential.
- Why this job: Make a real impact on patient health through cutting-edge technology and collaboration.
- Qualifications: Degree in Life Sciences or related field; experience in pharmaceutical development preferred.
The predicted salary is between 70000 - 90000 £ per year.
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 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.
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.
Responsibilities:
- 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.
Qualifications/Skills:
Basic Qualifications:
- 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.
Preferred Qualifications:
- 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.
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.
MSAT Molecule Steward in Ware employer: Gsk
GSK is an exceptional employer located in Greater London, offering a dynamic and inclusive work environment that fosters innovation and collaboration. As a Senior FinOps Product Manager, you will have the opportunity to drive impactful projects while benefiting from robust employee growth opportunities and a culture that values diverse perspectives. With a commitment to professional development and a focus on agile methodologies, GSK empowers its employees to thrive in their careers while contributing to meaningful advancements in cloud financial management.
StudySmarter Expert Advice🤫
We think this is how you could land MSAT Molecule Steward in Ware
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We think you need these skills to ace MSAT Molecule Steward in Ware
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Gsk!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Gsk that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Gsk!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Gsk, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Gsk
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Gsk that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Gsk’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
