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  • Early Clinical Development Medical Director, Oncology  

    - London
    GSK Oncology Early Clinical Development is seeking a highly skilled an... Read More
    GSK Oncology Early Clinical Development is seeking a highly skilled and motivated Early Clinical Development Medical Director- Oncology, to join our dynamic Oncology Research and Development team. In this role the successful candidate will create a strong link between Clinical Development and Pre-clinical/ Discovery teams to improve forward and reverse translation and, thereby, increase the success of our Oncology clinical portfolio in the prostate cancer space. This role offers a unique opportunity to bridge the gap between preclinical research and clinical development, ensuring the successful translation of innovative therapies from the lab to the clinic.The Early Clinical Development Medical Director- Oncology will report to the Executive Medical Director, Early Clinical Development Lead (ECDL)-GU, Oncology Clinical Development. The Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSK’s clinical portfolio and will also have responsibility for engaging in medical dialogues with relevant scientific and medical leaders in order to lead clinical data generation activities. This individual will also have a leading role in managing effective relationships with Key External Experts.This role requires a physician capable of developing and executing oncology clinical trials, in support of the successful clinical development, regulatory filing and initial market launch of a growing portfolio of innovative and transformational Oncology agents for patients with prostate cancer.Please note: This position requires an on-site office -based presence 2 to 3 days a week in the UK (London or Stevenage); Switzerland (Zug); US (Upper Providence, PA) or Poland (Warsaw).Key responsibilitiesCollaborate with physicians, scientists, regulatory professionals, biostatisticians, regulatory, executive staff and others in a complex matrix environment to develop and execute early phase interventional clinical trials for patients with prostate cancer.Ensure high quality protocol development aligned with the overall Clinical Development Plan for assets to effectively determine a medicine’s potential efficacy, safety profile, key areas of product differentiation and value to patient in the shortest possible timeframe. Use medical expertise to contribute to the end to end (protocol concept to final study report) to ensure scientific integrity and timely delivery of clinical trials which ensure consistency with the clinical development strategy for regulatory approvals, reimbursable medicines, and successful lifecycle management; demonstrate ability to incorporate global considerations into decision making Interpret and summarize study results consistent with objectives to define safety, efficacy, pharmacokinetic/pharmacodynamic, and patient reported outcomes, and applicability of data to the targeted prostate cancer patient population. Assume medical responsibility for clinical trials with active participation in real-time medical monitoring of studies, including patient eligibility assessment, study design questions, and addressing urgent safety questions (with inclusion of Safety/ PV as relevant).Assume responsibility for medical review of clinical trial data, both directly as needed and/or via oversight of delegated medical review. Oversee review of data packages intended for internal and/or external IDMCs.Review/monitor safety data in collaboration with pharmacovigilance group for active clinical studies.Participate in the authoring of clinical study reports and regulatory documents and collaborate with colleagues in Regulatory Affairs, CMC, Toxicology, Research, Pharmacology to respond to health authority and ethics committee queries.Collaborate with Principal Investigators in the evaluation and assessment of data during dose escalation and expansion studies and subsequent publications (abstracts, posters, manuscripts) associated with clinical data.Network extensively to develop long-term strategic partnerships with thought leaders both internally and externally, in support of GSK’s vision.Understand biological mechanisms, clinical strategy, scientific interpretation of disease and target-based literature. Serve as a core member of the Clinical Matrix Team for one or more assets in development.Represent Clinical Development on disease area strategy, integrated evidence and medical affairs strategy teams.Participate in Oncology Clinical Development-wide initiatives and workstreams as appropriate.Why You?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:Medical degree from accredited medical school​ Completion of a clinical residency program Experience in clinical research and development in OncologyExperience working in the pharmaceutical/biotechnology industry in prostate cancer. Preferred Qualifications:If you have the following characteristics, it would be a plus:Oncology experience in pharmaceutical/biotechnology industry preferredExperience in leading oncology clinical trials, including experience with study design, data review/interpretation and the overall clinical development processRobust knowledge of disease-specific research priorities, public health needs, competitor landscape, clinical practice trends and treatment guidelines evolution Experience in regulatory requirements to support registration, including knowledge and adherence to GCP principlesAgile and distributed decision-making – using evidence and applying judgement to balance pace, rigour and riskManaging individual and team performance.Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution.Implementing change initiatives and leading change.Sustaining energy and well-being, building resilience in teams.Continuously looking for opportunities to learn, build skills and share learning both internally and externally.Developing people and building a talent pipeline.Translating strategy into action - a compelling narrative, motivating others, setting objectives and delegation.Building strong relationships and collaboration, managing trusted stakeholder relationships internally and externally.Budgeting and forecasting, commercial and financial acumen.• If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $222,750 to $371,250. The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.The annual base salary in Poland for new hires in this position ranges from PLN 455,250 to PLN 758,750 gross, taking into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. Depending on the role and internal policies, the position may also be eligible for a bonus (if applicable and based on defined, non-discretionary criteria) and/or awards for exceptional performance (granted at the employer’s discretion). All statutory benefits will be maintained in accordance with Polish law. Other benefits may also be offered, which may include private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave & care of family member leave. More detailed information on the total reward package applicable to your role will be supplied during the recruitment process. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the market rate for the role.Please visit to learn more about the comprehensive benefits program GSK offers US employees. 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. Read Less
  • Senior Director, Head of Data Governance & Compliance  

    - London
    Make governance the engine of innovation: "Senior Director - Head Data... Read More
    Make governance the engine of innovation: "Senior Director - Head Data Governance & Compliance"If you believe data governance should innovation - not slow it down - this role is for you. We’re looking for a transformational leader to modernize how governance is designed, delivered, and experienced across R&D.Think policy-as-code, responsible AI ready controls, and federated ownership embedded in real workflows. Your mission is to ensure our data is trusted, compliant, and reusable by first intent, so scientists and product teams can move faster with confidence.Responsibilities:Set the strategy for R&D wide governance and compliance framework that directly underpins R&D digital transformation, grounded in real regulatory rigor (GxP, GDPR, HIPAA) and designed to enable innovation, not gate it. Build and modernize the governance function: standards, metadata/master data, lineage, and data quality, delivered through a federated model that empowers domains while keeping us interoperable. Embed governance in the flow of work by partnering with business and tech teams, making controls seamless, and measurable, across the lifecycle. Operationalize policy‑as‑code and adaptive compliance to reduce manual effort and accelerate decisions. Advance responsible AI governance (bias, explainability, monitoring) and pilot agentic AI to automate stewardship where it makes sense. Champion a reuse culture so value creation and interoperability become default behaviors across R&D. Measure impact with clear KPIs for governance effectiveness, data quality, compliance, and engagement, continuously iterating based on analytics and feedback. Who you are:A strategic, transformational leader who sees governance as an capable of influencing senior stakeholders and connecting business, data, and tech. Entrepreneurial operator: You’ll have the mandate to test emerging governance technologies, fail fast, and scale what works, grounded in evidence and user feedback.A builder who treats governance as a product: You design for user experience, informed by adoption metrics, and drive iterative improvement, not just policy documents.A collaborator who integrates with platform teams and programs to make governance invisible (but effective) in day-to-day decision making.A visible ambassador for our mission who can represent the DVO internally and with external partners and industry bodies.Basic Qualifications:Bachelor’s/master’s in computer science, Data Management, Mathematics, Statistics, Biostatistics, or related fields. 5+ yrs of transforming governance functions with innovative solutions that create competitive edge, from automation and policy-as-code to scalable reuse practices. 10+ yrs operating in ambiguous, fastmoving environments where you’ve had to , align stakeholders, and deliver measurable outcomes. Proven leadership in data governance/data management and complex R&D programs; fluency in regulatory frameworks (GxP, GDPR, HIPAA). Industry exposure to responsible AI and AI/ML lifecycle management; familiarity with Python/R/SQL and modern data platforms; governance certifications (DAMA/DMBOK, DCAM, EDM Council) appreciated.Preferred Qualifications:Proficiency in data science techniques, including data analysis, machine learning, and statistical modeling.Expertise in programming languages such as Python, R, SQL, and C++.Experience with data management tools and platforms (e.g., Hadoop, Spark, SQL databases).Knowledge of cloud computing platforms (e.g., AWS, Azure, Google Cloud).Ability to create and interpret data visualizations using tools like Tableau, Power BI, and D3.js.#GSK-LIPlease visit to learn more about the comprehensive benefits program GSK offers US employees. 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. Read Less
  • Key Account Manager - South West and Channel Islands  

    - Cornwall
    Description , as this will not be available post closure of the advert... Read More
    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.At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.Find out more: . This is a remarkable chance to be part of a newly formed specialist team, playing a pivotal role in helping GSK achieve its vision of bringing innovative medicines to patients in the UK.We’re excited about the future and look forward to hearing from you.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. Read Less
  • Supply Chain Data & Insights Manager  

    - London
    Job descriptionSite Name: Belgium-Wavre, UK – London – New Oxford Stre... Read More
    Job description
    Site Name: Belgium-Wavre, UK – London – New Oxford Street
    Posted Date: Jan 20 2026
    Job PurposeThe Supply Chain Data & Insights Associate plays a core role in ensuring the reliability, usability, and continuous evolution of the analytics solutions within the Supply Chain Control Tower, with a focus on Logistics and Regional Supply Chain.The position is responsible for maintaining and updating analytical interfaces, personas, landing pages, wheels, and data visualizations, ensuring that information is accurate, intuitive, and aligned with business processes. The Associate monitors data consistency, performs regular functional testing, maintains documentation, manages user access structures, and ensures tools are correctly displayed and functioning for different personas.The role also contributes to the enhancement of the Control Tower by helping rationalize existing solutions, updating libraries, identifying issues, and coordinating improvement actions. Additionally, the Associate will contribute to the development and optimization of GenAI agents by gathering business questions, maintaining versioning, and supporting model training to ensure agents provide clear, accurate, and actionable responses.This role requires strong analytical capabilities, attention to detail, learning agility, and the ability to work effectively in a global, multi-stakeholder environment where digital and data-driven approaches are central to decision making.Key ResponsibilitiesMaintain and update analytics solutions within the Control Tower for Logistics and Regional Supply Chain, ensuring data, interfaces, and visualizations remain accurate and aligned to defined standards.Contribute to the definition and upkeep of personas and user journeys, ensuring tools and visual elements are correctly mapped and intuitive for end users.Manage user access requests, workspace configurations, and persona-to-security mappings, ensuring the correct level of access for each user group in collaboration with P&I.Ensure all dashboards, landing pages, and CT Wheels are displayed correctly, with consistent and up-to-date data for each relevant persona.Maintain documentation across solutions, wheels, and the Control Tower library, ensuring materials are complete, current, and easy for users to reference.Perform regular functional and data-quality testing, identifying UI issues, data inconsistencies, or defects, and coordinating resolution with Tech when required.Monitor and track tickets or issues related to solutions in scope, ensuring they are logged appropriately and followed through to completion.Contribute to continuous improvement of the analytics landscape, including rationalisation of tools, identification of enhancement opportunities, and updates to shared libraries.Execute GenAI Business-As-Usual activities, ensuring agent behaviours are consistent, responses are reliable, and visualisations are correctly generated.Collect and curate business questions for GenAI model training, maintain version logs, and contribute to training and evaluation of GenAI agents to ensure high-quality outputs.Why YouBasic QualificationsUniversity degree or equivalent in a relevant field (Computer Science; Data Science; Data & Analytics; Supply Chain Management; Industrial Engineering; Mathematics; Statistics; or another quantitative or technical discipline.)2 to 5 years experienceFluent in EnglishPreferred Qualifications University degree in a related fieldAdditional certification or coursework in analytics, data modelling, AI/ML, or cloud technologies is an advantageStrong learning agilityCertifications or coursework in Data Analytics, AI/ML, Cloud technologies, or Data Engineering.Ability to translate business questions into analytical requirements, supporting persona design, user journeys, and tool configuration.Proficiency in SQL and basic-to-intermediate Python, with the ability to apply them to data extraction, transformation, and quality checks.Hands-on experience with BI or analytics tools, such as Power BI or similar platforms.Understanding of digital analytics concepts, such as root-cause analysis, diagnostic analytics, and performance interpretation.Exposure to modern data or cloud environments, ideally including tools within Microsoft Azure (e.g., Data Factory, Synapse, Databricks).Basic understanding of Large Language Model (LLM) technologies, with interest in prompt design, GenAI tools, or agent behaviour evaluation.Fluent in English (French is beneficial but not required)If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.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.Important notice to Employment businesses/ AgenciesGSK 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. Read Less
  • Sr. Manager, R&D Procurement, Laboratory Services  

    - Stevenage
    Are you looking to make a significant impact in a global organisation... Read More
    Are you looking to make a significant impact in a global organisation while driving innovation and delivering high-quality solutions? At GSK, we are committed to improving global health and empowering your career growth. We are currently seeking a Sr. Manager, R&D Procurement, Laboratory Services to join our Procurement team, supporting our R&D and QC laboratories across the globe.About the Role
    As the Sr. Manager, R&D Procurement, Laboratory Services, you will take ownership of sourcing and contract management for the Lab Services category, including instrument services, technical and general lab services, and lab tech. You will play a key role in developing and implementing category strategies, negotiating and executing contracts, and managing supplier relationships to ensure GSK’s performance, quality, and financial objectives are met.In this role, you will collaborate with global teams across multiple countries, requiring high cultural awareness, and work closely with senior leadership to deliver procurement strategies that maximize supplier leverage while driving continuous improvements. You will also be responsible for identifying opportunities to streamline processes and generate significant value for GSK.Key Responsibilities:Lead complex sourcing and category management activities for Lab Services within a global framework.Develop and implement category strategies aligned with GSK’s strategic goals.Plan, negotiate, execute, interpret, and maintain contracts while managing ongoing supplier negotiations.Collaborate with stakeholders and senior leaders to ensure successful deployment of strategies globally and regionally.Champion sourcing group management processes and policies across functions.Ensure compliance with risk, regulatory, and quality requirements in all supplier interactions.Lead end-to-end procurement processes, driving continuous improvement, in-house vs. third-party vs. outsourcing strategies.Manage and monitor supplier relationships outside of the enterprise SRM structure for this category.Collaborate with other global procurement groups to identify synergies and optimize supplier relationships.Generate value in terms of quality, delivery, cost, and contribute significantly to GSK’s goals.About You
    We are looking for a strategic thinker with strong problem-solving and analytical skills, excellent communication abilities, and the confidence to engage and challenge senior leaders. The ideal candidate will have a solid foundation in procurement, supply chain, business, or finance, along with experience in laboratory capabilities or scientific services provisions. You will be comfortable navigating complex global environments and possess a strong understanding of cultural differences in negotiations and supplier relationships.Qualifications and Experience Required:Minimum: A university degree in Procurement, Supply Chain, Business, Finance, or related fields.Preferred: Master’s degree in Procurement, Business, Finance, or a relevant scientific discipline.Relevant experience in procurement supporting laboratory capabilities or scientific services.Proven negotiation and contract management skills, with the ability to deliver quality, timely, and compliant agreements.Strong leadership and stakeholder management skills, including collaboration with senior leaders across R&D and Supply Chain.Exceptional communication skills, including English proficiency (written and oral); additional languages are a plus.Deep understanding of supplier capabilities, market trends, and business processes.Why GSK?
    At GSK, we are united by our mission to help people do more, feel better, and live longer. We foster a culture of innovation, collaboration, and inclusion, where you’ll have the opportunity to grow and make a lasting impact on global health. As part of our Procurement team, you’ll play a vital role in delivering solutions that improve lives while achieving GSK's strategic objectives.Ready to Apply?
    If you’re excited by the prospect of joining an organisation that values your expertise, empowers your growth, and challenges you to deliver on a global scale, we want to hear from you. Apply today and help us transform the future of healthcare through innovative procurement strategies.Closing Date: 25th January 2026Why 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. Read Less
  • Fermentation technologist (Secondment)  

    - Irvine
    Job descriptionSite Name: UK - North Ayrshire - IrvinePosted Date: Jan... Read More
    Job description
    Site Name: UK - North Ayrshire - Irvine
    Posted Date: Jan 20 2026
    Fermentation Technologist - 12 Months Secondment / FTCClosing Date - 3rd February 2026 (COB)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
    You will support and improve fermentation processes. You will work closely with colleagues in process development, manufacturing, quality, and engineering. We value curiosity, clear problem-solving, and a hands-on approach. This role offers chances to grow your technical skills, lead investigations, and help deliver medicines that make a real difference. Join us to unite science, technology and talent to get ahead of disease together.

    Responsibilities
    This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
    - Operate and optimise fermentation processes from lab scale to production scale, following safety and quality standards.
    - Plan, run and document fermentation trials, sampling strategies and process characterisation studies.
    - Troubleshoot process deviations and lead root cause analyses with clear corrective actions.
    - Analyse process and analytical data to identify trends and propose improvements.
    - Support technology transfers, validation activities and protocol preparation for scale-up.
    - Work with cross-functional teams and suppliers to maintain equipment, raw material quality and process robustness.

    Why You?

    Basic Qualification
    We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
    - Degree in biotechnology, microbiology, biochemical engineering or a related science, or equivalent experience.
    - Experience working with fermentation/bioreactor systems in a regulated manufacturing or industrial laboratory environment.
    - Practical skills in aseptic technique, sterile sampling and bioprocess operation.
    - Familiarity with process documentation and good manufacturing practice (GMP) requirements.
    - Strong analytical skills and experience working with process data and standard software tools (Excel, data capture systems).
    - Clear written and verbal communication skills and ability to work well in teams.

    Preferred Qualification
    If you have the following characteristics, it would be a plus:
    - Experience with scale-up from development to commercial fermentation operations.
    - Knowledge of downstream processing interfaces and key process parameters for biologics.
    - Experience with process modelling, statistical tools or Design of Experiments (DoE).
    - Familiarity with automation systems, SCADA or distributed control systems used in bioprocessing.
    - Track record of leading investigations, change controls or corrective actions in a regulated setting.
    - Awareness of sustainability considerations in biomanufacturing and process optimisation.

    Work Arrangement
    This role is fulltime on-site in Irvine in the United Kingdom.

    What we offer
    You will join a collaborative team focused on learning and continuous improvement. You will have opportunities to develop technical and leadership skills. We welcome applicants from all backgrounds and encourage people who bring different perspectives. If you are ready to apply your fermentation skills to meaningful work, we would love to hear from you. Apply now and help us get ahead of disease together.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/ AgenciesGSK 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/ Read Less
  • Medical Director- Oncology Clinical Development  

    - London
    At GSK, we have bold ambitions for patients, aiming to positively impa... Read More

    At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.
    Find out more:


    Position Summary:GSK Oncology Clinical Development is seeking a highly skilled and motivated Clinical Development Medical Director- Oncology, to join our dynamic Oncology Research and Development team. In this role the successful candidate will create a strong link between Clinical Development and other functions in the clinical matrix team to increase the success of our Oncology clinical portfolio in the GU cancer space.The Clinical Development Medical Director- Oncology will report to the Executive Medical Director, Clinical Development Lead (CDL)-GU, Oncology Clinical Development. The Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSK’s clinical portfolio and will also have responsibility for engaging in medical dialogues with relevant scientific and medical leaders in order to lead clinical data generation activities. This individual will also have a leading role in managing effective relationships with Key External Experts.This role requires a physician capable of developing and executing oncology clinical trials, in support of the successful clinical development, regulatory filing and initial market launch of a growing portfolio of innovative and transformational Oncology agents for patients with prostate cancer.Please note: This position requires an on-site office -based presence 2 to 3 days a week in the UK (London or Stevenage); Switzerland (Zug); US (Upper Providence, PA. Waltham, MA); or Poland (Warsaw).Key responsibilities:Collaborate with physicians, scientists, regulatory professionals, biostatisticians, regulatory, executive staff and others in a complex matrix environment to develop and execute early phase interventional clinical trials for patients with prostate cancer.Ensure high quality protocol development aligned with the overall Clinical Development Plan for assets to effectively determine a medicine’s potential efficacy, safety profile, key areas of product differentiation and value to patient in the shortest possible timeframe. Use medical expertise to contribute to the end to end (protocol concept to final study report) to ensure scientific integrity and timely delivery of clinical trials which ensure consistency with the clinical development strategy for regulatory approvals, reimbursable medicines, and successful lifecycle management; demonstrate ability to incorporate global considerations into decision making Interpret and summarize study results consistent with objectives to define safety, efficacy, pharmacokinetic/pharmacodynamic, and patient reported outcomes, and applicability of data to the targeted prostate cancer patient population. Assume medical responsibility for clinical trials with active participation in real-time medical monitoring of studies, including patient eligibility assessment, study design questions, and addressing urgent safety questions (with inclusion of Safety/ PV as relevant).Assume responsibility for medical review of clinical trial data, both directly as needed and/or via oversight of delegated medical review. Oversee review of data packages intended for internal and/or external IDMCs.Review/monitor safety data in collaboration with pharmacovigilance group for active clinical studies.Participate in the authoring of clinical study reports and regulatory documents and collaborate with colleagues in Regulatory Affairs, CMC, Toxicology, Research, Pharmacology to respond to health authority and ethics committee queries.Collaborate with Principal Investigators in the evaluation and assessment of data during dose escalation and expansion studies and subsequent publications (abstracts, posters, manuscripts) associated with clinical data.Network extensively to develop long-term strategic partnerships with thought leaders both internally and externally, in support of GSK’s vision.Understand biological mechanisms, clinical strategy, scientific interpretation of disease and target-based literature. Serve as a core member of the Clinical Matrix Team for one or more assets in development.Represent Clinical Development on disease area strategy, integrated evidence and medical affairs strategy teams.Participate in Oncology Clinical Development-wide initiatives and workstreams as appropriate.Why You?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:Medical degree from accredited medical school​ Completion of a clinical residency program Experience in clinical research and development in OncologyExperience working in the pharmaceutical/biotechnology industry in GU prostate cancer.Preferred Qualifications:If you have the following characteristics, it would be a plus:Oncology experience in pharmaceutical/biotechnology industry preferredExperience in leading oncology clinical trials, including experience with study design, data review/interpretation and the overall clinical development processRobust knowledge of disease-specific research priorities, public health needs, competitor landscape, clinical practice trends and treatment guidelines evolution Experience in regulatory requirements to support registration, including knowledge and adherence to GCP principles• If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $222,750 to $371,250. • If you are based in another US location, the annual base salary range is $222,750 to $371,250. The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.The annual base salary in Poland for new hires in this position ranges from PLN 455,250 to PLN 758,750 gross, taking into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. Depending on the role and internal policies, the position may also be eligible for a bonus (if applicable and based on defined, non-discretionary criteria) and/or awards for exceptional performance (granted at the employer’s discretion). All statutory benefits will be maintained in accordance with Polish law. Other benefits may also be offered, which may include private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave & care of family member leave. More detailed information on the total reward package applicable to your role will be supplied during the recruitment process. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the market rate for the role.Please visit to learn more about the comprehensive benefits program GSK offers US employees. 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. Read Less
  • Project Controls Director - EU, UK  

    - London
    Description , as this will not be available post closure of the advert... Read More
    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. 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. Read Less
  • Key Account Manager - South West and Channel Islands  

    - Gloucester
    Description , as this will not be available post closure of the advert... Read More
    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.At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.Find out more: . This is a remarkable chance to be part of a newly formed specialist team, playing a pivotal role in helping GSK achieve its vision of bringing innovative medicines to patients in the UK.We’re excited about the future and look forward to hearing from you.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. Read Less
  • Medical Director- Oncology Clinical Development  

    - Stevenage
    At GSK, we have bold ambitions for patients, aiming to positively impa... Read More

    At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.
    Find out more:


    Position Summary:GSK Oncology Clinical Development is seeking a highly skilled and motivated Clinical Development Medical Director- Oncology, to join our dynamic Oncology Research and Development team. In this role the successful candidate will create a strong link between Clinical Development and other functions in the clinical matrix team to increase the success of our Oncology clinical portfolio in the GU cancer space.The Clinical Development Medical Director- Oncology will report to the Executive Medical Director, Clinical Development Lead (CDL)-GU, Oncology Clinical Development. The Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSK’s clinical portfolio and will also have responsibility for engaging in medical dialogues with relevant scientific and medical leaders in order to lead clinical data generation activities. This individual will also have a leading role in managing effective relationships with Key External Experts.This role requires a physician capable of developing and executing oncology clinical trials, in support of the successful clinical development, regulatory filing and initial market launch of a growing portfolio of innovative and transformational Oncology agents for patients with prostate cancer.Please note: This position requires an on-site office -based presence 2 to 3 days a week in the UK (London or Stevenage); Switzerland (Zug); US (Upper Providence, PA. Waltham, MA); or Poland (Warsaw).Key responsibilities:Collaborate with physicians, scientists, regulatory professionals, biostatisticians, regulatory, executive staff and others in a complex matrix environment to develop and execute early phase interventional clinical trials for patients with prostate cancer.Ensure high quality protocol development aligned with the overall Clinical Development Plan for assets to effectively determine a medicine’s potential efficacy, safety profile, key areas of product differentiation and value to patient in the shortest possible timeframe. Use medical expertise to contribute to the end to end (protocol concept to final study report) to ensure scientific integrity and timely delivery of clinical trials which ensure consistency with the clinical development strategy for regulatory approvals, reimbursable medicines, and successful lifecycle management; demonstrate ability to incorporate global considerations into decision making Interpret and summarize study results consistent with objectives to define safety, efficacy, pharmacokinetic/pharmacodynamic, and patient reported outcomes, and applicability of data to the targeted prostate cancer patient population. Assume medical responsibility for clinical trials with active participation in real-time medical monitoring of studies, including patient eligibility assessment, study design questions, and addressing urgent safety questions (with inclusion of Safety/ PV as relevant).Assume responsibility for medical review of clinical trial data, both directly as needed and/or via oversight of delegated medical review. Oversee review of data packages intended for internal and/or external IDMCs.Review/monitor safety data in collaboration with pharmacovigilance group for active clinical studies.Participate in the authoring of clinical study reports and regulatory documents and collaborate with colleagues in Regulatory Affairs, CMC, Toxicology, Research, Pharmacology to respond to health authority and ethics committee queries.Collaborate with Principal Investigators in the evaluation and assessment of data during dose escalation and expansion studies and subsequent publications (abstracts, posters, manuscripts) associated with clinical data.Network extensively to develop long-term strategic partnerships with thought leaders both internally and externally, in support of GSK’s vision.Understand biological mechanisms, clinical strategy, scientific interpretation of disease and target-based literature. Serve as a core member of the Clinical Matrix Team for one or more assets in development.Represent Clinical Development on disease area strategy, integrated evidence and medical affairs strategy teams.Participate in Oncology Clinical Development-wide initiatives and workstreams as appropriate.Why You?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:Medical degree from accredited medical school​ Completion of a clinical residency program Experience in clinical research and development in OncologyExperience working in the pharmaceutical/biotechnology industry in GU prostate cancer.Preferred Qualifications:If you have the following characteristics, it would be a plus:Oncology experience in pharmaceutical/biotechnology industry preferredExperience in leading oncology clinical trials, including experience with study design, data review/interpretation and the overall clinical development processRobust knowledge of disease-specific research priorities, public health needs, competitor landscape, clinical practice trends and treatment guidelines evolution Experience in regulatory requirements to support registration, including knowledge and adherence to GCP principles• If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $222,750 to $371,250. • If you are based in another US location, the annual base salary range is $222,750 to $371,250. The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.The annual base salary in Poland for new hires in this position ranges from PLN 455,250 to PLN 758,750 gross, taking into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. Depending on the role and internal policies, the position may also be eligible for a bonus (if applicable and based on defined, non-discretionary criteria) and/or awards for exceptional performance (granted at the employer’s discretion). All statutory benefits will be maintained in accordance with Polish law. Other benefits may also be offered, which may include private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave & care of family member leave. More detailed information on the total reward package applicable to your role will be supplied during the recruitment process. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the market rate for the role.Please visit to learn more about the comprehensive benefits program GSK offers US employees. 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. Read Less

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