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Commercial Launch Lead - Hepatology We are seeking an experienced commercial launch leader to drive the UK strategy for a new hepatology medicine within the specialty portfolio. In this role you will Own the end to end UK launch strategy, translating brand objectives into a detailed operational plan and driving go/no go decisions. Drive cross functional and above country alignment among Medical, Sales, Health Outcomes, Market Access, Regulatory, and Supply teams. Establish, monitor, and report launch KPIs and readiness metrics; lead performance reviews and provide optimisation actions. Leverage market insights, real world evidence, and field feedback to continuously optimise tactics and convert learnings into action. Recruit, develop, and lead a high performing commercial team, embedding accountability, coaching, and collaborative ways of working. Lead and shape the evolving post launch UK brand roadmap, anticipating market shifts and using clinical and RWE to maximise sustained patient access. Basic Qualifications & Skills Bachelor's degree or equivalent in life sciences, marketing, business or related field. Extensive commercial experience in pharma/biotech with demonstrable ownership of commercial launch strategy and delivery. Proven experience coordinating cross functional teams (Medical, Market Access, Regulatory, Supply, Sales) to deliver launch plans. Track record of people leadership: hiring, coaching, and managing performance within commercial teams. Strong stakeholder management and influencing skills, with excellent written and verbal communication. Proven ability to manage complex projects in a fast paced, matrixed environment. Preferred Qualifications & Skills Prior launch leadership for a specialty product in the UK, preferably hepatology or virology. Multi country or above country launch experience with partnership to regional and global brand teams. Success engaging payers, KOLs and NHS decision makers, with strong influencing and negotiation skills. Experience navigating the UK market access environment (NICE/HTA, commissioning routes), engaging clinical/NHS stakeholders and working within ABPI requirements. Strong capability using market insights, analytics and real world evidence to inform commercial strategy. Ability to translate clinical and HEOR evidence into clear commercial value propositions and stakeholder facing materials. Equal Opportunity Employer Statement 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, military service or any basis prohibited under federal, state or local law.

Purpose of Onyx The Onyx Research Data Tech organization represents a major investment by GSK R&D and Digital & Tech, designed to deliver a step-change in our ability to leverage data, knowledge, and prediction to find new medicines. We are a full-stack shop consisting of product and portfolio leadership, data engineering, infrastructure and DevOps, data / metadata / knowledge platforms, and AI/ML and analysis platforms, all geared toward: Building a next-generation data experience for GSK's scientists, engineers, and decision-makers, increasing productivity and reducing time spent on "data mechanics" Providing best-in-class AI/ML and data analysis environments to accelerate our predictive capabilities and attract top-tier talent Aggressively engineering our data at scale to unlock the value of our combined data assets and predictions in real-time Onyx Product Management is at the heart of our mission, ensuring that everything from our infrastructure, to platforms, to end-user facing data assets and environments is designed to maximize our impact on R&D. The Product Management team partners with R&D stakeholders and Onyx leadership to develop a strategic roadmap for all customer-facing aspects of Onyx, including data assets, ontology, Knowledge Graph / semantic search, data / computing / analysis platforms, and data-powered applications. We are seeking an experienced Senior Product Manager who will be accountable for designing and delivering the road map for molecule design products to support GSK Research and Development. This role will be pivotal in ensuring a cohesive enterprise level strategy towards molecule design solutions and will ensure our scientists have access to best-in-in-class technology products to improve research productivity and ultimately deliver new medicines for our patients. In this role you will: Own and lead the product roadmap, product development, launch and adoption of novel molecule design solutions to benefit the scientific community at GSK across multiple departments Play a key role in defining the strategic direction for molecule design tools with GenAI capabilities at the core Partner closely with the wider Onyx tech team, as well as R&D scientists and leaders, to deliver industry-leading cloud-based products and solutions with GenAI and agentic capabilities. Key Responsibilities: Product Strategy and Roadmap: Develop and execute a comprehensive product strategy and roadmap for molecule design solutions and tools, aligned with the Onyx's overall product vision and objectives. Customer Understanding: Conduct in-depth customer research, gather customer insights, and engage with customers regularly to understand emerging requirements. Product Planning and Definition: Collaborate with stakeholders to define product requirements, features, and specifications based on customer feedback, product vision, and business goals. Agile Product Development: Work closely with portfolio and engineering teams in an agile environment to ensure successful and timely delivery of product releases, including prioritization, sprint planning, and backlog management. GenAI Product and Capability Upgrade: Spearhead the development of a new class of AI Agents, powered by LLMs and Generative AI, designed to autonomously execute complex scientific research tasks like hypothesis generation, experimental design, and data interpretation. Design and productize the human-agent interaction layer, moving beyond traditional UIs to create conversational and goal-driven interfaces that allow scientists to delegate multi-step tasks and interpret the outputs of autonomous GenAI systems. Own the product lifecycle for models and agents, leading the strategy for data acquisition, model fine-tuning, and the development of APIs/agents that allow them to be leveraged as "tools" by other agents and systems. Model-In-The-Loop Design: Structuring products so that R&D users can easily challenge, verify, and provide feedback to improve the agentic tools and underlying models (human-guided iteration). Demonstrate Human + AI collaboration with minimum friction to drive user adoption. Lead highly technical product discussions with engineering leaders, translating ambiguous scientific objectives into precise requirements for fine-tuning foundational models, vector databases, and multi-agent system architectures. Cross-Functional Collaboration: Collaborate with both tech and RD teams, including DevOps & Infrastructure, data engineering, computing platform engineering, data & knowledge platform engineering, program management teams and RD data leadership teams, to align product strategies, gather input, and drive successful implementation plans. Product Launch and Adoption: Lead product launches, ensuring effective communication, training, and support materials to drive successful product adoption and customer satisfaction. Product Performance and Optimization: Continuously monitor product performance, collect and analyze data, and drive iterative improvements to enhance product usability, performance, and customer experience. Why you? Qualifications & Skills: We are looking for professionals with these required skills to achieve our goals: Bachelors degree in Bioinformatics, Computational Biology, cheminformatics, AI/ML, Computer Science, Software Engineering, or related discipline. Significant experience in product management with a proven track record of shipping 0-to-1 software products powered by AI/GenAI, LLMs, or autonomous agents in a commercial or large-scale enterprise setting. Demonstrated experience defining product strategy for modern applications, including hands-on experience with technologies core to AI systems such as vector databases, MLOps, retrieval-augmented generation, and model fine-tuning. Direct product management experience designing and launching AI agents that can utilize tools (APIs, function calling) to perform complex, multi-step actions and reason about their environment. Deep technical fluency with cloud-native architectures (e.g., AWS, GCP, Azure), API design, and the infrastructure required to serve and scale LLM-based applications Preferred Qualifications & Skills: Master's degree or PhD in Bioinformatics, Computational Biology, Computational Chemistry, Data Science, Computer Science/Software Engineering, Cloud Computing or related discipline. Hands-on software engineering or data science experience in a GenAI-focused team prior to transitioning into product management. Familiarity with the architecture of modern transformer-based models and the strategic product trade-offs between using proprietary models (e.g., GPT-4, Claude), open-source models (e.g., Llama, Mistral), and fine-tuning custom models. Experience building products that manage or interpret complex, unstructured biomedical data Extensive knowledge of bioinformatics, computational biology, or cheminformatics, and a strong vision for how agentic AI can revolutionize the drug discovery process. Extensive product experience designing, optimizing, and implementing Model Context Protocols (MCP) for LLM-powered agents, including advanced strategies for prompt engineering, context window management, memory architectures (e.g., short-term, long-term memory), and ensuring model coherence over extended multi-turn interactions. Hands-on experience with product management tools such as Confluence, Jira, Miro, Monday, Notion, etc. Previous experience in life science industry or biopharma R&D is a plus. Closing Date for Applications: Tuesday 6th January 2026 (COB) Please note: As we approach the holiday season, our recruitment team and hiring managers will have limited availability between now and early January. We encourage you to apply and will review all applications, however response times may be longer than usual, and interviews may be scheduled after the New Year. We appreciate your understanding and look forward to connecting soon! 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. During the course of your application, you will be requested to complete voluntary information which will be used to monitor the effectiveness of our equality and diversity policies. Your information will be treated as confidential and will not be used in any part of the selection process. If you require a reasonable adjustment to the application / selection process to enable you to demonstrate your ability to perform the job requirements, please contact . This will help us to understand any modifications we may need to make to support you throughout our selection process. 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 . click apply for full job details

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. Position Summary You will join a production team that fills and packs dermatology products for patients. You will move materials, support production lines, and help maintain high standards of quality and safety. You will work closely with production, quality, engineering and warehouse colleagues. We value people who are reliable, practical and willing to learn. This role offers hands on skills, clear development routes and a chance to contribute to work that helps people live healthier lives by uniting science, technology and talent to get ahead of disease together. Responsibilities Stage, retrieve and transfer components, containers and finished packs to support fill and pack lines. Prepare and check batch documentation, labels and reconciliations to maintain traceability. Operate material handling equipment such as pallet trucks and lift trucks safely. Support temperature controlled handling and storage for sensitive materials. Clean and prepare components and production areas to required standards. Report and escalatue production, quality or stock discrepancies and help resolve issues. Basic Qualification Minimum of 5 GCSEs or equivalent, or relevant manufacturing experience. Experience in a production, warehouse or manufacturing environment. Ability to read and follow written procedures and complete accurate records. Comfortable working on site in controlled or clean environments. Willingness to work shift patterns as required for production. Team player with clear communication and a willingness to learn. Preferred Qualification Experience in pharmaceutical or healthcare manufacturing. Experience with digital production or warehouse systems (for example MES or ERP). Experience handling temperature controlled or frozen materials. Familiarity with Good Manufacturing Practice (GMP) principles. Forklift or counterbalance truck licence or training. Experience participating in continuous improvement activities. Working arrangement This role is on site at our Barnard Castle manufacturing facility. Shift work is required to meet production needs. 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. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at where you can also request a call. For more information, please visit

EHS Lead 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 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. 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 You will be accountable for developing, implementing, and managing comprehensive EHS programs that ensure compliance with regulatory requirements, protect employee health and safety, and minimize the environmental impact of manufacturing operations. The EHS Lead will drive continuous improvement initiatives, foster a culture of safety and sustainability, and collaborate with cross functional teams to support the production of high quality pharmaceutical products. Responsibilities Regulatory Compliance: Ensure the manufacturing site adheres to all relevant local, state, and federal EHS regulations, as well as GSK's internal policies and standards. Risk Management: Identify potential EHS risks and implement effective mitigation strategies to minimize hazards and promote a safe working environment. Incident Investigation: Lead thorough investigations of EHS incidents, accidents, and near misses, and develop corrective and preventive actions to prevent recurrence. Training and Education: Develop and deliver comprehensive EHS training programs to empower employees with the knowledge and skills necessary to maintain a safe and healthy workplace. Emergency Preparedness: Develop, implement, and regularly update emergency response plans and procedures, ensuring the site is well prepared for any potential emergencies. Continuous Improvement: Drive continuous improvement initiatives in EHS performance through the implementation of best practices, innovative solutions, and ongoing monitoring and evaluation. Sustainability Initiatives: Lead efforts to minimize the environmental impact of manufacturing operations, including waste reduction, energy efficiency, and resource conservation. Collaboration: Work closely with cross functional teams, including Operations, Quality, and Engineering, to integrate EHS considerations into all aspects of site activities and projects. Performance Metrics: Develop and maintain EHS performance metrics and reporting systems to track progress, identify trends, and communicate results to site leadership and corporate EHS teams. Leadership and Culture: Foster a culture of safety, health, and environmental responsibility by promoting awareness, engagement, and accountability at all levels of the organization. Basic Qualifications Degree in science, engineering, environmental health, occupational safety, or equivalent experience. Demonstrable years' experience in EHS with leadership or supervisory responsibility. Strong knowledge of UK health, safety and environmental legislation. Practical experience in a regulated manufacturing or process industry. Proven experience in incident investigation, risk assessment and emergency planning. Comfortable influencing senior stakeholders and working within a site leadership team. Preferred Qualifications NEBOSH Certificate or Diploma, or equivalent professional EHS qualification. Experience in pharmaceutical, chemical or other highly regulated manufacturing environments. Experience managing environmental permits and wastewater treatment compliance. Membership of a recognised professional EHS body. Experience leading EHS audits, assurance programmes and behaviour based safety initiatives. Track record of coaching and developing EHS teams and embedding continuous improvement. Work Location: This role is based in Barnard Castle, UK and is a 100% site based role. Closing Date for Applications: 14th April 2026 GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, colour, 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.

A leading global biopharma company is seeking a Supplier Quality Audit Lead to oversee compliance audits of suppliers within the Pharma Supply Chain. You will conduct GMP assessments, develop corrective action plans, and ensure effective communication with stakeholders. The role requires strong auditing experience, a degree in Life Science, and excellent English communication skills. The position involves considerable travel across Europe, representing 30% to 50% of responsibilities.

A leading biopharmaceutical company in the UK is seeking an experienced Senior Product Manager to lead the strategy and delivery of core AI/ML platform products. This role will focus on establishing a unified enterprise approach to model training and deployment, ensuring R&D teams build and operationalize AI models effectively. Candidates should have significant experience in product management, ideally within AI-powered applications, and a strong track record of collaboration with scientific teams. The position offers a competitive salary and opportunities for growth.

Principal Scientist, Biophysics Large Molecule Research drives the discovery and development of innovative biopharmaceutical medicines, advancing a diverse portfolio from early antibody discovery through to molecular engineering and comprehensive biological and physicochemical characterisation. We are seeking an experienced and motivated Principal Scientist in Biophysics to join our dynamic research team. The successful candidate will play a pivotal role in developing and applying advanced biophysical techniques to support drug discovery and development projects. This is a key hire for those with a proven track record in label free interaction analysis of protein protein interactions and deconvolution of complex data in support of mode of action studies, data interpretation, and innovative problem solving within the biopharmaceutical sector. In this role you will Design, plan, and execute experiments using biophysical techniques such as Surface Plasmon Resonance (SPR), Biolayer Interferometry (BLI), size exclusion chromatography (SEC), hydrophobic interaction chromatography (HIC) and differential scanning fluorimetry (DSF) throughout the large molecule discovery process. Analyse, interpret, and report complex biophysical data, ensuring high standards of scientific rigour and reproducibility. Lead work to develop and optimise experimental protocols to improve throughput and data quality. Drive data handling strategies, including effective storage, management, and reuse to maximise research impact and compliance with data integrity standards. Collaborate cross functionally with colleagues in protein engineering, discovery biology, and informatics to deliver integrated project solutions. Present findings to internal teams and external stakeholders; contribute to scientific publications and conferences as appropriate. Mentor junior scientists and contribute to the continuous improvement of laboratory best practices. Why you? Basic Qualifications & Skills: We are looking for professionals with these required skills to achieve our goals: PhD (or equivalent experience) in Biophysics, Biochemistry, or a related discipline. Significant hands on demonstratable expertise with SPR or similar technologies (e.g., Biacore, Octet, Carterra), and epitope binning technologies for characterisation of protein protein and/or protein antibody interactions. Experience working with high throughput screening and automation platforms in a fast paced environment in an industry or a relevant research environment. Demonstrated ability to analyse, interpret, and visualise complex datasets; proficiency in data management and reuse strategies. Strong understanding of molecular interaction theory and its application to drug discovery. Demonstrated experience leading matrix teams. Preferred Qualifications & Skills Please note the following skills are not necessary, just preferred, if you do not have them, please still apply: Project leadership experience. Familiarity with AI/ML tools for data analysis. Track record of scientific publications or patent filings. Closing Date for Applications 19th April 2026 (COB) 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. If you require adjustments to our process to assist you in demonstrating your strengths and capabilities, contact .

A leading biopharmaceutical company in Stevenage is seeking a Principal Scientist in Biophysics to develop advanced techniques for drug discovery. The role involves designing experiments, analyzing complex data, and collaborating with cross-functional teams. Candidates should have a PhD in Biophysics or a related field, hands-on experience with SPR, and a strong understanding of protein interactions. This position offers a unique opportunity to contribute to innovative solutions in biopharmaceutical research.