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Site Name: USA - Pennsylvania - King of Prussia Posted Date: Sep 30 2025 The purpose of this role is to develop, implement and administer input into in-process quality systems and/or electronic quality systems for the production of biopharmaceutical products to ensure compliance with GSK internal procedures, policies, standards, and worldwide regulatory expectations. This is done through direct intervention between this role and other staff in the facility. This role provides quality support to project teams and to routine operating teams. This position will provide guidance and training to new and existing employees in the Quality Compliance department. This role ensures adherence to frequency of oversight mandate in the Quality oversight schedule. In addition, this role would support periodic product reviews, internal quality agreements, and post inspection communication assessment and regulatory compliance. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:<ul><li>Perform and /or manage adherence to frequency of oversight mandate in Quality oversight schedule.</li><li>Manage and/or support the following Quality Compliance systems (periodic product review, internal quality agreements, post inspection communications, market specific requests, deviation regulatory assessment and change control). </li><li>Support batch connecting process for change controls and release with Operational Quality.</li><li>Support special projects, such as quality improvement initiatives.</li><li>Lead and Support internal audits (Level 1/Level 2) and prepare summary reports. Collect and evaluate information to assist in internal and vendor audits. Support L3/L4 inspections in various functions ranging from control room support, scribe, SME.</li><li>Lead and support completion of annual product reviews and reports for products across the site.</li><li>Support closure of Quality Compliance records including corrective and preventative actions, change controls.</li><li>Update departmental documents such as SOPs as required. Perform the review of technical documents as required.</li><li>Attend meetings as a Quality representative and provide input, including providing updates at Quality Council.</li><li>Support implementation of global strategies as required by the GSK business and QMS.</li></ul>Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals:<ul><li>BS or BA in Quality, Laboratory, or Manufacturing.</li><li>1+ year's industrial experience in quality, operations, or assurance functions.</li><li>Or 5+ years of work experience can be considered in Lieu of education</li></ul> Preferred Qualifications: If you have the following characteristics, it would be a plus:<ul><li>Experience in biologics manufacturing, quality systems, including documentation, regulatory compliance, vendor management, and internal auditing</li><li>Knowledge of GMP's, NIH Guidelines, FDA and other regulatory agency requirements preferred.</li><li>Good written communication, organizational, and computer skills. Good interpersonal and verbal skills required. Able to function within team based organization.</li><li>Able to prioritize and decide appropriate course of actions. Effective at implementing decisions. </li><li>Able to interact with peers, subordinate and senior personnel in multidisciplinary environment including engineering, facility operations, production and QC.</li></ul> Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

public

QA System Coordinator (Biopharma)

Site Name: USA - Pennsylvania - King of Prussia Posted Date: Sep 30 2025 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. Join our team as an Automation Engineer and t ake area ownership while providing engineering and technical support for process controls and manufacturing execution systems in the Biopharmaceutical Operations facility. Evaluate and develop technology, plan and implement modifications, troubleshoot and support process controls and manufacturing execution systems and assist in night shift troubleshooting activities during processing operations . This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:<ul><li>Provide technical support of site automation systems and network infrastructure. Critical systems include DeltaV DCS and Syncade MES. </li><li>Collaborate with building stakeholders throughout the automation lifecycle: gather system/end user requirements; complete design, implementation, and testing/validation of changes; maintain documentation; maintain and monitor various systems.</li><li>Adhere to GxP expectations for proper change management and system documentation.</li><li>Troubleshoot and diagnose problems with process controls and manufacturing execution systems; generate recommendations and then develop/execute solutions to correct and resolve.</li><li>Drive continuous improvement and support capital projects.</li><li>Adhere to, develop, and continuously improve the operation and maintenance procedures for process controls and manufacturing execution systems.</li><li>Support the maintenance and upkeep of the operational technology environment through administration of systems, networks, databases, and accounts. This includes servers, hosts, and analytical equipment.</li><li>Support site technology related to systems integration and digital transformation initiatives. </li><li>Work in a way that models respect for safety and EHS, quality compliance, data integrity, and engineering standards.</li></ul>Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals:<ul><li>BS/BA in engineering, life sciences, biology</li><li>OR 4 years of experience working with control system or in a biopharmaceutical environment will be considered in Lieu of education</li><li>Experience in design, programming, start-up, and troubleshooting of process control systems and instrumentation PLC such as Emerson DeltaV, Allen Bradley etc.</li></ul>Preferred Qualifications: If you have the following characteristics, it would be a plus:<ul><li>Prior experience in the design, programming, and troubleshooting of Emerson Syncade or similar MES systems is strongly preferred.</li><li>Prior experience in systems/account administration, network design, and server troubleshooting is strongly preferred.</li><li>Prior experience coding Visual Basic and similar languages is strongly preferred.</li><li>Experience working in a GMP environment is strongly preferred.</li><li>Prior experience in the design, programming, start-up, and troubleshooting of PLC (Allen Bradley) systems is preferred.</li><li>A demonstrated ability to interact well with peers and senior personnel in multidisciplinary teams involving scientific, engineering, and operational disciplines is required.</li><li>Ability to diagnose problems, generate options, prioritize issues, select optimal solutions, and implement decisions/resolve problems is required.</li><li>Knowledge in current standards of control system platforms and computer system validation is preferred.</li><li>Training/certification related to one or more of the following areas is preferred: DeltaV, Syncade, Network Design, Systems administration, Database administration, PLCs, Visual Basic and similar languages, Instrumentation</li></ul> Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Automation Engineer

Site Name: USA - Pennsylvania - Upper Providence, GSK HQ, UK - Hertfordshire - Stevenage Posted Date: Sep 30 2025 Director, Patient Centered Outcomes Locations: Upper Providence, PA. GSK HQ or Stevenage, UK. Hybrid 2-3 days per week. Additional flexible arrangements considered on case-by-case basis. Job Purpose: As a Director of Patient-Centered Outcomes (PCO) you will apply technical expertise to plan and support evidence development strategies for Patient Reported Outcomes (PRO)/Clinical Outcome Assessment (COA)-related endpoints across GSK's portfolio. GSK's PCO team plays an integral role in the development of integrated evidence plans to ensure that strong PRO/COA strategies support a patient-centric understanding of our drug development across Respiratory, Immunology and Inflammation, Infectious Diseases, Vaccines and Oncology. Our mission is to deliver by implementing strong measurement science to capture the patient voice in demonstrating the value of our products to patients, physicians, payers, and regulators. The team has educational backgrounds across a range of PRO/COA disciplines and experience in pharmaceutical, regulatory, and academic settings. We work in a matrix environment with close partnership across GSK functions including Clinical Development, Regulatory Affairs, Biostatistics, Medical Affairs, Commercial and Patient Focused Development. We are well connected with external initiatives exploring innovative approaches to define, implement and interpret patient centric endpoints in drug development. The PCO team maintains a sharp focus on the value of patient-centric outcomes across the portfolio. We want to ensure that each clinical program has a well-characterized, innovative PRO/COA strategy that is defined early in the development lifecycle and has clear plans to develop evidence that supports PRO/COA-related endpoints. Key Responsibilities: <ul><li>Define and oversee the execution of strategies for the rigorous development and implementation of PRO/COAs across GSK's portfolio.</li><li>Guide the development, validation, analysis, interpretation, and utilization of PRO/COA instruments in the context of clinical trials and/or observational studies.</li><li>Work cross-functionally (e.g., clinical operations, biostats teams) to ensure the value of patient-centric endpoints is communicated clearly and that PRO/COAs are implemented and analyzed appropriately in clinical trials (and are accurately described in statistical analysis plans, study reports and publications).</li><li>Support key communications with regulatory bodies by developing targeted questions related to the PRO/COA endpoint strategy and identifying the critical evidence needed for meetings to support GSK's patient-centric endpoint strategies.</li><li>Support broader publication strategy by planning for and contributing to external publications (e.g., scientific abstracts and peer-reviewed manuscripts) which present PRO-related results from clinical trials and/or PRO development and validation studies.</li><li>Maintain awareness of scientific and regulatory changes across GSKs drug development programs.</li><li>Pursue ongoing learning to understand and adopt evolving methodologies and guidelines (including those from regulatory authorities) and communicate findings to functional groups as needed.</li></ul> Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: <ul><li>Master's or Doctoral degree in Psychology, Psychometrics, Social Sciences, Outcomes Research, Health services research, Public Health, Epidemiology, Pharmacy, or a closely related discipline.</li><li>7+ years of experience in a related role, including demonstrated experience with PRO/COA development and implementation in a consulting and/or pharmaceutical company environment. </li><li>Experience in pharmaceuticals, particularly in drug and vaccine development, with demonstrated experience in clinical trial planning and execution.</li><li>Experience with FDA Patient Focused Drug Development Guidance.</li><li>Experience with planning and managing PRO development and validation projects.</li></ul><ul><li>Experience in inclusion of COA endpoints in clinical trials and analysis of PRO data.</li><li>Experience in managing internal stakeholders through to executive levels.</li><li>Working knowledge or experience in psychometric methods for the validation of PROs/COA endpoints.</li><li>Working knowledge or experience in the evolving methods and regulatory environment with respect PRO/COA.</li></ul> Preferred Qualifications: If you have the following characteristics, it would be a plus: <ul><li>Understanding of healthcare markets and regulatory and reimbursement decision making, especially in relation to the global use of PRO data in drug and vaccine development.</li><li>Strong verbal and written communication skills.</li></ul>LI-GSK* Hybrid* Please visit GSK US Benefits Summary 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Director, Patient Centered Outcomes

Site Name: USA - Pennsylvania - Philadelphia, Durham Blackwell Street Posted Date: Sep 30 2025 The Director, Product Management - Field Technology will lead the management, optimization, and adoption of sales systems , and data to drive commercial effectiveness within the US Commercial Organization. This role is accountable for developing and executing strategic enhancements, ensuring system performance, and enabling field teams with the necessary tools and insights to optimize execution. The Director will act as a key partner to Sales, Digital, Data & Tech , Commercial Operations, and Analytics, ensuring alignment across functions and fostering collaboration to deliver impactful solutions. By managing a team dedicated to field technology and engaging with internal and external vendor partners this leader will deliver solutions that enhance productivity, automate processes, and support the organization's broader strategic priorities. Key Responsibilities Product Management & Sales Systems Strategy <ul><li> Act as the business lead for sales systems supporting field teams across multiple therapeutic areas, leveraging strong product management principles to prioritize and deliver impactful solutions. </li><li> Develop and implement a product roadmap for data-driven field technology improvements, considering advancements in capabilities (internal & external), ensuring alignment with business needs, strategic objectives, and coordination between personal and digital engagement channels. </li><li> Drive system enhancements, configurations, and integration efforts with internal Global Tech partners and external vendors, including Veeva CRM, Contract Sales partners, and other sales enablement platforms. </li><li> Lead cross-functional product management initiatives to enhance sales force productivity through system automation, process efficiencies, and innovative solutions. </li><li> Oversee the configuration, integration, and optimization of field tools, including Veeva CRM, leveraging external data sources, content solutions, and master data management (MDM). </li><li> Conduct user acceptance testing (UAT), training coordination, deployment planning, and user onboarding in partnership with Sales Operations. </li><li> Monitor system performance, user adoption, and support issues to drive resolution and continuous improvement while maintaining proper documentation, including user guides, SOPs, and validation protocols where required. </li></ul> Field Support & Adoption <ul><li> Serve as the liaison between field sales teams and technology partners, ensuring seamless system performance and prompt issue resolution. </li><li> Collaborate with Sales Training / Sales Operations and / or external vendor partners to create training materials, user guides, and best practices to support field adoption. </li><li> Establish and monitor adoption metrics, proactively identifying areas for improvement and driving user engagement. </li><li> Conduct onboarding and systems training for field teams to ensure effective use of tools and technologies in partnership with Sales Operations. </li></ul> Data & Analytics Alignment <ul><li> Partner with Commercial Data and Analytics teams and / or external vendor partners to ensure sales teams have access to timely, meaningful insights and dashboards that inform decision-making. </li><li> Work with technology teams to maintain data integrity, governance, and compliance within sales systems to include , support of Aggregate Spend reporting requirements. </li><li> Analyze system utilization data and performance metrics to provide strategic recommendations to leadership. </li></ul> Team Management, Stakeholder Engagement & Collaboration <ul><li> Build trusted relationships with Sales Leadership, Digital Data and Technology, Marketing, and Commercial Operations partners to align system capabilities with commercial priorities. </li><li> Manage relationships with external vendors, handling system reliability, ongoing enhancements, vendor selection, contract negotiations, and service-level agreements. </li><li> Lead and develop team members to build relevant skills and knowledge to deliver Field Technology priorities - near term and future roadmap. </li><li> Lead workshops and user interviews to gather feedback for continuous improvement and optimization of field technologies. </li></ul> Core Competencies <ul><li> Accountability for Results:Focus on key strategic objectives , maintain high standards of performance, and take ownership of driving change. </li><li> Strategic Thinking & Problem Solving:Make decisions with a long-term view, considering impacts on customers, patients, employees, and the business. </li><li> Patient & Customer Centricity: Maintain an ongoing focus on the needs of customers and key stakeholders. </li><li> Impactful Communication:Communicate with clarity, respect, and influence at all levels to achieve the best outcomes. </li><li> Respectful Collaboration:Value diverse perspectives and foster partnerships that enhance collective goals. </li><li> Empowered Development:Take an active role in professional development and promote growth within the team. </li></ul> Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: <ul><li>Bachelor's degree in computer science, Information Technology, or a related field.</li><li> 10 + years of experience in CRM management, field technology, or sales operations with clear ownership of field technology applications. </li><li> Hands-on expertise in Veeva CRM, and other sales enablement platforms </li><li> Proven ability to lead system implementation, enhancements, and field adoption initiatives </li><li> Proven ability to lead direct line and matrix teams. </li><li> Strong analytical, problem-solving, and product management skills. </li><li>E xperience working cross-functionally with Sales, IT, Commercial Operations, and Analytics. </li><li> Experience in the pharmaceutical, biotech, or healthcare industry. </li></ul>Preferred Qualifications: If you have the following characteristics, it would be a plus: <ul><li> Familiarity with AI-driven sales analytics and emerging field technologies. </li><li> Master 's degree in computer science, Information Technology, or a related field. </li></ul>#LI-GSK Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Director, Product Management, Field Technology

Site Name: USA - North Carolina - Zebulon Posted Date: Sep 30 2025 As a Production Senior Process Operator, you will Operate, challenges and cleans equipment, according to appropriate to SOPs, JSAs, and batch documents to deliver high quality products manufactured in a safe way to fulfil the needs of the supply chain. Monitors equipment for excessive rejects. Performs all duties in accordance with regulatory and OSHA requirements. Ability to changeover and set up equipment to design specifications including performing all SAP changeover tasks. Identified as the SME for all systems interaction and operations and proficient at all SOPs, JSAs, and OSW for the relevant area documents. Leads the creation of standards/systems to increase business results. Key Responsibilities: <ul><li>Operates, challenges, replenishes consumable supplies, cleans equipment, and all the duties needed by the business in accordance with cGMPs, Batch Documentation, SOPs, ZSPs and JSAs as required and responsible for maintaining inspection readiness of area with minimal supervision.</li><li>Actively participates and owns monitoring equipment for excessive rejects/ stoppages and utilizes performance data to escalate any problems occurring in the area that affects product quality, safety and other aspects of line performance.</li><li>Trained in the GSK Production System standards (i.e., 5s, standard work, problem solving, Gemba, process confirmations, and performance management) towards the goal of Zero Accidents, Zero Defects, and Zero Waste.</li><li>Participates in performance management entry, steps 1-3 of problem solving, and performing/maintaining OSW and 5S.</li><li>Delivers against safety, quality, waste & performance objectives defined by strategy deployment and identifies and recommends areas for process improvement or alternative operating methods to increase efficiency.</li><li>Recognized as an expert on operations/process and possesses the ability to troubleshoot and resolve minor equipment production stoppages. </li><li>Operator possesses considerable knowledge of the job and is reliable and able to produce high quality and high quantity work.</li><li>Utilizes systems/applications required for job performance (i.e. DELTA, my Learning, Free Weigh, DISY, Active Plant, IP21, SAP basic transactions for meeting production supply, etc.).</li><li>Works in coordination with other associates, assistants, and/or technicians to carry out daily job responsibilities, including recognizing and assisting with troubleshooting technical issues and providing information to the next supervisory level.</li><li>Demonstrates the ability to describe the technological theory of operation, product flow through equipment, and able to identify the function and purpose of all sensors, limit switches, and proximity sensors.</li><li>Demonstrates the ability to conduct equipment set up changeovers and start of batch activities to the designed specifications without start up issues. Ability to certify on multiple technologies and flow to the work as needed by the business.</li></ul> Why you? Basic Qualifications: We are looking for professionals with these minimum required skills to achieve our goals:<ul><li>High School Diploma or GED</li><li>5+ years experience in Production Operator role</li><li>3+ years experience working at GSK</li><li>OJT certified in all work centers in packaging or the majority of work centers in manufacturing</li><li>Demonstrated performance in all Process Operator job roles</li></ul> Preferred Qualifications: We are looking for professionals with these required skills to achieve our goals:<ul><li>Associate Degree or equivalent education</li><li>Basic reading, writing and mathematical skills</li><li>Basic computer skills and understanding and operational computer skills, MS Word, and MS Excel.</li><li>Ability to work accurately with figures and information</li><li>Ability to use and analyze data effectively</li><li>Must be mechanically inclined with the ability to learn the operation, read gauges and instrumentation, and any equipment related to the production of medical devices and/or pharmaceutical products</li><li>Strong attention to detail and ability to create and follow detailed documentation.</li><li>Ability to follow both written and verbal instruction.</li></ul> Skills: <ul><li>Basic reading, writing and mathematical skills</li><li>Advanced computer skills and understanding and operational computer skills, MS Word, and MS Excel</li><li>Ability to proficiently utilize basic hand tools</li><li>Ability to work accurately with figures and information</li><li>Must be mechanically inclined with the ability to learn the operation, read gauges and instrumentation, and any equipment related to the production of medical devices and/or pharmaceutical products</li></ul> Traits: <ul><li>Visual inspection and attention to detail</li><li>Strong attention to detail and ability to create and follow detailed documentation.</li><li>Ability to follow both written and verbal instruction.</li><li>Thorough understanding of Overall Equipment Effectiveness</li><li>Advanced computer skills (focused on MS Office) use software to analyze data & troubleshoot</li><li>Ability to work independently</li><li>Ability to train others on job related tasks</li><li>Ability to set up equipment to scale measurements without assistance</li><li>Competent at problem solving utilizing 6 step process that identifies root cause</li></ul> Physical Job Requirements: <ul><li>Ability to climb, kneel, stoop, balance, crawl, crouch, reach, sit, stand, walk, push, pull, grasp, feel, talk, hear, lift, and perform tasks as defined by the specific role.</li><li>Ability to work overtime as needed.</li><li>Must be able to wear gloves, eye protection, and protective clothing as required by the specific job role.</li><li>Must be able to handle up to 40 lbs. of materials</li><li>Must be able to work inside a manufacturing environment where there may be exposure to noise, moving mechanical parts, and various drug compounds as the specific role mandates.</li><li>Must be able to flow to the work as needed and operate at a high energy fast-paced environment</li><li>Ability to learn at a rapid pace to support training module expectations</li><li>Ability to work up to 12.5 hrs. in one shift</li></ul> About the Zebulon Site GSK's Zebulon site is a global supplier of Respiratory and Solid Dose medicines to patients around the globe and the largest GSK Pharmaceutical secondary manufacturing site in North America. The site is located less than 30 minutes from downtown Raleigh, Wendell, Knightdale, Rocky Mount and Wake Forest. Key differentiators about GSK and Zebulon: <ul><li>Our commitment to inclusion and diversity - we see diversity as a critical advantage of ours</li><li>Our focus on cultivating a positive work environment that cares for our employees</li><li>Demonstrated opportunities for continued career growth driven by individual ambition</li><li>Leaders that care about their teams and growth of both individuals and the company</li><li>A priority focus on Safety and Quality</li><li>Clean and GMP compliant work environment </li><li>Onsite cafeteria </li><li>Onsite gym </li><li>Temperature-controlled </li><li>Licensed onsite Health & Wellness clinic </li></ul> Work Environment This role is **on-site** and requires physical activity throughout the shift. You'll work in a temperature-controlled manufacturing environment with protective gear provided. If you're looking for a role where you can grow your career and contribute to a team that values safety and quality, we encourage you to apply! Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Senior Process Operator (MDI PKG) (1st/2nd Shift)

Site Name: Durham Blackwell Street, Bengaluru Luxor North Tower Posted Date: Sep 30 2025 We're seeking a highly skilled and hands-on AI Solution Architect to join our team and help drive the development of a cutting-edge AIOps platform. This individual will play a pivotal role in designing and implementing AI-driven solutions that transform IT Operations-enhancing automation, observability, and incident response across complex enterprise environments. As a key member of our architecture team, you will collaborate with data scientists, engineers, and IT stakeholders to architect AI-driven solutions that proactively detect, diagnose, and resolve operational issues across complex infrastructure and application landscapes. We are seeking someone who enjoys building real world systems in production environments. Key Responsibilities:<ul><li>Architect and lead the development of an enterprise-grade AIOps platform leveraging machine learning, deep learning, and advanced analytics.</li><li>Design scalable AI pipelines for anomaly detection, predictive analytics, root cause analysis, and intelligent alerting.</li><li>Collaborate cross-functionally with engineering, DevOps, and IT teams to integrate AI capabilities into existing operational workflows and tools.</li><li>Evaluate and select appropriate technologies, frameworks, and cloud-native services in Azure and GCP to support real-time data ingestion, processing, and model deployment.</li><li>Ensure platform reliability and performance, with a focus on scalability, security, and maintainability.</li><li>Mentor and guide engineering teams on best practices in AI architecture and model lifecycle management.</li><li>Stay current with emerging trends in AIOps, MLOps, and IT automation to continuously evolve the platform</li></ul>Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: <ul><li>Bachelor's or master's degree in computer science, Data Science, Machine Learning, or related field</li><li>Experience as a Solution Architect or AI/ML Architect in enterprise environments.</li><li>3+ years of hands-on experience building AIOps platforms and solutions in IT environments.</li><li>Strong understanding of IT Operations, infrastructure monitoring, incident management, and observability tools.</li><li>Hands-on experience with AI/ML frameworks (e.g., TensorFlow, PyTorch, Scikit-learn) and data engineering tools (e.g., Spark, Kafka, Airflow) and knowledge graphs.</li><li>Proficient in Python and familiar with key AI/ML libraries (e.g., TensorFlow, PyTorch, HuggingFace).</li><li> Strong familiarity with cloud platforms such as Azure and Google Cloud Platform (GCP), including their native Data and AI/ML toolsets and services like ADLS, Azure Machine Learning, Azure Foundry, GCS and GCP Vertex AI. Experience with container orchestration technologies like Kubernetes, and hands-on expertise in working with Large Language Models (LLMs) and Generative AI tools. </li><li>Excellent communication and stakeholder management skills.</li><li>Have good mentoring skills to guide team members.</li></ul>Preferred Qualifications: If you have the following characteristics, it would be a plus: <ul><li>Experience with log and metrics analysis, time-series forecasting, and NLP for IT ticket classification.</li><li>Knowledge of MLOps practices for model deployment, monitoring, and governance.</li><li>Exposure to tools like ServiceNow, Datadog, Prometheus, Grafana, ELK Stack, etc</li><li>Certified in AI engineering in Azure and GCP</li></ul>#LI-GSK Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

AI Solutions Architect

Site Name: USA - Texas - Dallas Posted Date: Sep 30 2025 Why join us? 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 are a focused biopharma company. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and advanced technologies, investing in four core therapeutic areas (Infectious Diseases, HIV, Respiratory, Immunology and Oncology). Our Ahead Together strategy means intervening early to prevent and change the course of disease, helping to protect people and support healthcare systems. It's an exciting time in GSK as we bring outstanding people together to do work that matters and impacts the world's health. Our commitment to innovation in the immunology space has been unwavering for over a decade, positioning us as pioneers in addressing the diverse needs of patients. As we look to the future, the synergy between our talented workforce and our commitment to scientific excellence will drive our continued growth and success. What we're looking for: This role will provide you the opportunity to lead key activities, career growth, and the ability to do impactful work: Responsibilities include the following: Key Responsibilities: Describe the key deliverables to be achieved by the post holder and the ongoing responsibilities of the role<ul><li>Provide Scientific Knowledge, Business Acumen, and Customer Engagement expertise to specialist customers in support of a GSK biologic product. </li><li>To understand the reimbursement/distribution landscape for specialist customers and identify the appropriate resources (e. g. Payer Relations Managers, HUB, headquarter approved materials) to refer customers to appropriate resource for reimbursement and distribution choices, always working within GSK guidelines and values. </li><li>Maintain knowledge and data, which are constantly changing, with respect to severe asthma therapeutic expertise. </li><li>Provide product educational programs/in-services to customers.</li><li>Work within Compliance guidelines and GSK values always. </li><li>Develop strategies and tactics to generate sales.</li><li>Develop and implement strategies specific to each customer within an account (i.e., Rheumatologists, Nephrologists, nurses, mid-levels, business/office managers). </li><li>Develop and maintain strong working relationships with Marketing, Payer Relations Managers (Market Access), Medical (MSLs), and other functions within GSK. </li><li>Effectively manage allocated resources</li><li>Provide outstanding customer service by responding to our customers' requests, inquiries and needs.</li></ul>Basic Qualifications:<ul><li>Bachelor's degree </li><li>Ability to travel domestically as necessary, which in some territories may include overnight travel up to 30% </li><li>Valid driver's license. </li><li>Must be able and willing to drive or operate a vehicle - driving is an essential function of this role.</li><li>The selected candidate will be hired at the appropriate level based on experience<ul><li>Specialty Account Specialist (grade 8): 5+ years of pharmaceutical/medical device experience.</li><li>Senior Specialty Account Specialist (grade 7): 12+ years of pharmaceutical/medical device experience. </li></ul></li></ul>Preferred Qualifications: If you have the following characteristics, it would be a plus: <ul><li> Specialty Products that utilize the Buy & Bill or Specialty pharmacy modes of distribution. </li><li>Expertise in working with Payer Reimbursement Managers</li><li>Biologic/Rare Disease/Immunology Sales experience </li></ul>#LI-Remote Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Specialty Account Specialist, Immunology

Site Name: Durham Blackwell Street, USA - Pennsylvania - Philadelphia Posted Date: Sep 29 2025 GSK is one of the world's preeminent pharmaceutical and healthcare companies. We take pride in leading a healthcare revolution. Through disruptive approaches in R&D and commercial business processes, our Data & Analytics team integrates, simplifies, and unlocks all our data. This drives innovation, decision-making, and allows us to better serve our patients, healthcare professionals, and consumers This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:<ul><li>Develop and deliver high quality, machine learning solutions to uncover learnings for the US Anti-Infective business at the patient, HCP/EE segment, and health system level aligned with analytical priorities for:<ul><li>Segmentation</li><li>Measurement</li><li>Omnichannel</li><li>Resource Allocation and Optimization</li><li>Experimental design (test/control) analyses</li></ul></li><li>Understand data science opportunities, based on analytical knowledge, needed to deliver innovative solutions to uncover drivers of gaps in scientific understanding and patient unmet needs to improve strategic opportunities.</li><li>Act as a data science expert, by learning and contributing to GSKs' data science community to grow their data skill skills, build best practices, and grow data science literacy within the organization</li><li>Earn the trust of stakeholder partners to drive data-driven decisions through active engagement, advanced analytics expertise, demonstrated learning, and business knowledge.</li><li>Establish and define project plans, proactively seek inputs needed to complete results according to plan and deliver milestones according to plan.</li><li>Collaborate on cross-matrix teams and demonstrate subject matter expertise with other teams/functions to drive efficiencies and seamless decision making.</li><li>Use storytelling, powerful visualizations to demonstrate power of utilizing data science with business partners and analytics team members which enable fact-based recommendations that inspire usage for data driven decisions</li></ul>Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: <ul><li>Bachelor's degree with 3+ yrs of Industry experience, master's or PhD with 1+ yrs of Industry experience.</li><li>1+ years' experience applying analytics and statistical skills in a business setting </li><li>1+ years' professional experience with analytics tools/languages and visualization tools</li><li>Proficiency in analytics tools/languages such as SQL, Python, PySpark, and visualization tools</li><li>Proficiency in statistical and ML models</li><li>Proactively identify areas for analysis, including the potential application for machine learning, and contribute to problem-solving.</li></ul>Preferred Qualifications: If you have the following characteristics, it would be a plus: <ul><li>Enthusiasm for leveraging Real World Data</li><li>Analytic curiosity to develop innovative solutions to solve complex problems.</li><li>Effective communicator w/ strong business acumen knowledge</li><li>Understanding of business needs and ability to develop appropriate solutions</li><li>Demonstrate teamwork and strong collaborative partnerships</li><li>Familiarity with healthcare-related datasets, such as claims data (e.g., Express Scripts, CVS Caremark, IQVIA), pharma retail data, co-administration analysis, and buy-and-bill processes.</li></ul> #LI-GSK Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Data Scientist

Site Name: Field Worker - USA Posted Date: Sep 29 2025 TITLE: Enterprise Business Director - Cigna GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems. Our diverse portfolio consists of vaccines, specialty medicines, and general medicines. Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges. In this role, you will serve as GSK's Account Director responsible for Ascent Health Services and all of Cigna/ESI (Commercial and Medicare PBMs). Predominately focused on Cigna/Ascent traditional respiratory, specialty and oncology businesses. Ability to thrive in a team is essential. You will be a key part of the Cigna Enterprise team. Responsibilities include execution of GSK's strategic positioning, delivering brand value propositions, negotiating optimal formulary access and effectively managing business relationships. Role will require 25% travel. Key Responsibilities<ul><li>Ensure optimal formulary access for GSK products within Ascent and Cigna/ESI's National Commercial and Medicare formularies. In addition:</li><li>Develop and lead strategy to meet or exceed goals of GSK products with a heavy focus on alignment with the Business Units, Finance, Pricing and Contracting, and the Market Access Leadership Team.</li><li>Lead the development of internal business case documents with emphasis on account specific strategy and financial objectives.</li><li>Lead the execution of GSKs Pharmacy and Medical Benefit contracts.</li><li>Develop an extensive understanding of the customers' organizational goals in order to assess their needs and develop plans/programs to meet both the needs of the customer and those of GSK.</li><li>Work closely with your Enterprise teammates by championing the Enterprise Mindset" and sharing strategic ideas to foster innovative approaches to enhance GSKs position in the market.</li><li>Collaborate regularly with other Account Directors as well internal stakeholders responsible for Cigna in other channels (Trade, Specialty Pharmacy, Vaccines)</li><li>Interface with the Pricing and Contracting team, Market Access Strategy, Access and Reimbursement Managers, and Contract Management and Operations to maximize product access and pull-through.</li><li>Work closely with the Contract Analyst Manager and Enterprise Market Analytics Director to develop Business Case Documents for internal GSKs Contract Review Board and Strategic Pricing Council.</li><li>Work closely with the Contract Development Manager on all contract terms & conditions, understanding language intent, and execution of the Pharmacy and Medical Benefit Contracts.</li><li>Maintain a high level of knowledge of the managed care industry and healthcare trends.</li><li>Maintain a high level of knowledge of Respiratory, Oncology, Specialty and Vaccine trends.</li><li>Understand and apply Compliance Policies and Procedures (CPP).</li></ul> Why You? Basic Qualifications: We are looking for professionals with the required skills to achieve our goals:<ul><li>Bachelor's Degree</li><li>Minimum 5+ years of pharmaceutical experience</li><li>3+ years of account management, contracting, sales management, or product management experience.</li><li>Valid Driver's License ability to travel up to 25%.</li></ul>Preferred Qualifications: If you have the following characteristics, it would be a plus:<ul><li>PBM contracting experience.</li><li>Payer marketing and/or contract management experience MBA and/or advanced clinical/science degree</li><li>Deep knowledge of Specialty, Oncology, and Vaccine payer/distribution.</li><li>Understanding of reimbursement and control mechanisms by PBMs Excellent negotiation and/or major account sales skills Demonstrated ability to establish and maintain relationships with key customers and internal stakeholders Deep knowledge of the managed care industry and healthcare trends</li><li>Understanding of the laws and regulations covering providers and payers Ability to apply Compliance Policies and Procedures (CPP) in unstructured and fluid situations.</li><li>Strong analytical skills</li><li>Excellent communication skills (written & verbal)</li><li>Strong presentation skills</li><li>Full accountability for meeting strategic objectives</li></ul>This role is field-based, with flexibility for hybrid work arrangements. Travel is required to attend customer meetings and conferences. Join us in shaping the future of healthcare by building meaningful partnerships and driving impactful solutions. #LI-GSK Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Enterprise Account Director - Cigna

Site Name: USA - Pennsylvania - Upper Providence, UK - Hertfordshire - Stevenage Posted Date: Sep 26 2025 As a Principal Scientist in the Translational Unit, working in Neurodegeneration or Renal Disease, you will play a critical role in bridging preclinical and early clinical proof of concept studies by designing and performing translational assays in human-derived cells, tissues, and biofluids. This is a lab-based position with mandatory on-site presence at either the Upper Providence, Pennsylvania (USA) or Stevenage (UK) laboratory sites. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following... <ul><li>Design and execute laboratory experiments to advance scientific understanding and support drug discovery in neurodegeneration or renal disease.</li><li>Support identification and validation of clinical biomarkers and development of clinically deployable biomarker assays.</li><li>Apply expertise in multiple capabilities such as ELISA/MSD/Quanterix, Western/JESS, flow cytometry, gene/protein expression analysis, proteomics, and other omics platforms.</li><li>Troubleshoot assays effectively and develop alternative approaches when necessary, working closely with preclinical statistics and other relevant teams to ensure robust study design.</li><li>Maintain accurate and detailed laboratory records in alignment with data integrity expectations and ensure compliance with all relevant protocols and safety guidelines.</li></ul> Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: <ul><li>PhD in a scientific discipline (e.g., Molecular Biology, Genetics, Immunology, or related field) with relevant laboratory experience.</li><li>4+ years' experience in translational and biomarker development.</li><li>Experience with handling of primary human cells and laboratory techniques such as immunoassays (ELISA, MSD, Quanterix), multi-color flow cytometry, and gene expression analysis.</li><li>Experience in renal disease or neurodegeneration disease areas.</li></ul>Preferred Qualifications: If you have the following characteristics, it would be a plus: <ul><li>Excellent problem-solving skills and ability to critically analyze scientific data.</li><li>Strong written and verbal communication skills, with the ability to effectively present scientific findings to multidisciplinary internal and external stakeholders in a balanced, clear, and precise manner.</li><li>Proven ability to balance priorities across multiple objectives, meeting timelines while maintaining attention to detail and high-performance standards.</li><li>Able to independently define strategic approach to tackle specific project or department goals.</li><li>Ability to work independently as well as collaboratively in a team-oriented environment.</li><li>Resourcefulness to access cutting-edge technologies, tools, reagents, biosamples, biomarker expertise, and research capabilities.</li></ul> Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Principal Scientist Translational Science - Neurodegeneration or Renal Disease

Site Name: USA - Massachusetts - Cambridge, GSK HQ, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper Providence Posted Date: Sep 26 2025 GSK is seeking a highly skilled and experienced Executive Medical Director to lead an exciting and expanding Hepatology program, advancing an asset through late-stage development while exploring opportunities for life-cycle management to maximize its therapeutic and commercial impact. This position reports to the VP Clinical Development, CRH, GI & Renal in the Respiratory, Immunology & Inflammation Research Unit (RIIRU) Advanced Pipeline Unit (APU). About RIIRU: The Respiratory, Immunology and Inflammation Research Unit (RIIRU) was formed in 2024 to identify and advance novel molecular targets with genetic associations to disease based on the foundational observation that targets with human genetic evidence supporting their causal role in the intended indication improves clinical success by two-fold. The remit of RIIRU is to identify novel targets based on human genetics, develop assets for clinical studies, and perform trials through to submission for approvals . This goal is enabled through strategic external (e.g., Flagship Pioneering, Vesalius, Muna Therapeutics and others) and GSK-internal partnerships (Research Technologies). PLEASE NOTE: This career opportunity requires an on-site office presence (minimum of two days a week) in one of GSK's US (PA or MA) or UK (London - New Oxford Street or Stevenage) sites. Key Responsibilities<ul><li>Strategic Leadership: Provide medical and scientific leadership for a hepatology asset, driving strategy to achieve clinical, regulatory, and commercial milestones while ensuring alignment with GSK's strategic priorities.</li><li>Late-Stage Drug Development: Oversee the design, initiation, execution, and closure of late-stage clinical trials, including Phase 3 studies, ensuring delivery of high-quality data to support regulatory approval and commercialization.</li><li>Global Regulatory Interactions: Lead critical regulatory activities, including dossier submissions, preparation for meetings with health authorities (e.g., FDA, EMA, PMDA), and responses to regulatory queries.</li><li>Life-Cycle Management: Identify, develop, and execute strategies to expand the asset beyond its primary indication, exploring significant life-cycle opportunities to maximize its therapeutic and commercial potential.</li><li>Cross-Functional Collaboration: Leverage significant experience working across a complex cross-functional matrix to partner with clinical, translational, commercial, regulatory, and scientific teams.</li><li>Innovation and Competitive Intelligence: Monitor emerging trends, competitor activities, and advancements in hepatology and related fields to identify opportunities for differentiation and strategic growth.</li><li>Team Leadership: Lead and mentor a high-performing team, fostering professional development, providing clear direction, and ensuring alignment with GSK's values and objectives.</li><li>External Representation: Act as a key representative of GSK's RIIRU in hepatology, engaging with external stakeholders, scientific forums, and professional organizations to advance the company's visibility and influence in this therapeutic area.</li></ul>#LI-GSK Basic Qualifications<ul><li>Medical degree and clinical medical specialty training board qualification/registration.</li><li>Experience in the global pharmaceutical/biotechnology industry in the field of hepatology.</li><li>Experience in clinical research and drug development, with a focus on hepatology.</li><li>Line-management experience overseeing medical directors and/or clinical scientists as well as leading matrix teams within a clinical development setting.</li><li>Experience in late-stage hepatology drug development, including Phase 2 and Phase 3 clinical trial design, initiation, execution, and closure.</li></ul>Preferred Qualifications<ul><li>Medical degree and clinical medical specialty training board qualification/registration in Gastroenterology or Hepatology.</li><li>Demonstrated success in life-cycle management, including identifying opportunities for indication expansion and strategic development beyond primary indications.</li><li>Experience with regulatory interactions, including submissions, strategy meetings, and negotiations with health authorities.</li><li>Understanding of the clinical and scientific landscape in hepatology, experience in advancing innovative therapies.</li><li>Experience in translational medicine and biomarker development.</li></ul> Please visit GSK US Benefits Summary 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Executive Medical Director, Hepatology

Site Name: USA - Pennsylvania - Upper Providence, GSK HQ, UK - London - New Oxford Street Posted Date: Sep 26 2025 The Director, Content Approval - Quality and Training is a critical position within Global Medical Information and Content Approval. The Director will support the Sr Director of Quality, Training and Operations in the development, implementation and embedment of key training and capability initiatives to support the strategic objectives of content approval, including ABPI examination and certification and management monitoring. The role requires strong leadership, decision-making, collaboration, vendor management, management monitoring and process implementation skills to enhance the efficiency, compliance, and effectiveness of content approval deliverables. The Director serves as a key partner for both Medical Affairs and Commercial organizations. Key Responsibilities: Quality Oversight: <ul><li>Manage quality control processes (incl. established KPI and SLAs, where applicable) within content approval including ABPI examination and certification.</li><li>Identify, assess, and execute/manage actions to mitigate risks associated with content approval operations.</li><li>Review and identify trends from reports on quality performance, compliance status, operational effectiveness and improvement initiatives. Recommend possible actions for continuous improvement.</li><li>Engage with GMI CA Leadership, team members and key business partners identifying opportunities for continuous improvements, sharing performance metrics and managing risks & mitigations</li><li>Assist as a subject matter expert on content approval process, serve as a key point of contact for audits, and inspections, and manage remediation efforts related to content approval.</li><li>Develop and implement robust content approval management monitoring and ensure timely completion of relevant CAPAs.</li><li>Act as the deputy global process owner for the process of approval of promotional and non-promotional materials and partner with the global process owner to ensure process is optimal and drive adequate understanding and application of the same to ensure high quality and compliant content at GSK. </li></ul> Training: <ul><li>Identify training needs and develop and deliver a comprehensive training strategy for Content Approval team members, ensuring alignment with internal processes and external regulatory requirements and business needs.</li><li>Ensure vendors for content review and approval have the necessary training on relevant GSK requirements/processes.</li><li>Develop, deliver and maintain a comprehensive onboarding curriculum for the Content Approval team members.</li><li>Partner with ABPI Directors, GMI&CA leadership and internal stakeholders (e.g., Compliance, Legal, Regulatory, Commercial) to ensure training content remains current and relevant.</li><li>Conduct refresher training on content review and approval process, as needed, to ensure high quality and compliance.</li></ul>Why You? Basic Qualifications: We are looking for professionals with the required skills to achieve our goals: <ul><li>Master's/Graduate Degree in Life Sciences or Healthcare</li><li>6+ years of pharmaceutical industry experience</li><li>3+ years of Medical Affairs experience</li><li>Strong understanding of content approval requirements including external regulations (e.g. ABPI Code)</li><li>Experience in quality and compliance oversight including audits and inspections</li><li>Experience in the development and delivery of training and onboarding programs</li></ul>Preferred Experience: If you have the following characteristics, it would be a plus: <ul><li>Experience in digital transformation and technology solutions to enhance training and operations.</li><li>Leadership experience in cross-functional teams within a matrixed organization.</li><li>Experience of working at both global and local country level</li><li>Flexible thinking - ability to analyze external environment and translate to strategy and gain support from others to implement a vision.</li><li>Ability to analyze external environment and translate to strategy.</li><li>Ability to work effectively with others, delegate appropriately and foster a strong culture of teamwork.</li><li>Ability to execute and embed change initiatives</li><li>Demonstrate capabilities to assess situation, flex and adjust as required to meet the demands of the business</li></ul> Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Director, Content Approval - Quality and Training

Site Name: USA - Pennsylvania - King of Prussia Posted Date: Sep 25 2025 At GSK, 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. We are looking to hire a MSAT Product Owner Associate Director to join the Manufacturing Science and Technology (MSAT) organization in Upper Merion. This is a site-based team, providing technical support to ensure Upper Merion Biopharm site goals and objectives areachieved. The primary objective role of MSAT is to ensure manufacturing processes are capable, compliant and productive while ensuring product quality. The site MSAT team is also responsible for delivering continuous improvements to the existing supply chains supported by UM Biopharm and working with global MSAT to execute technology transfers a nd implement process-related improvement programs across the product lifecycle. The MSAT Product Owner Associate Director, will lead a team of product owners to support the portfolio of clinical and commercial programs for Upper Merion. Product Owners are the single point of accountability for technology transfer, product lifecycle, CMC strategy, and technical execution for the biopharmaceutical assets manufactured Upper Merion. The individual supports the team to manage new product introduction, QbD, control strategy, and CPV development and maintenance, CMC dossier authoring and health authority questions, and technical product strategy and process efficiency / continuous improvements. The individual is also expected to drive continuous improvement in these spaces, aligning with platform standards and integrating digital solutions. In addition, this individual will be expected to work in a cross-functional matrix environment, including stakeholders in other departments within UM biopharm (i.e. production, quality, engineering), and global MSAT, R&D, global regulatory, and global quality. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: <ul><li>Serve as the Upper Merion lead for a team of site product owners for clinical and commercial programs</li><li>Drive the delivery of right-first time new product introduction and commercial lifecycle management, including CMC regulatory file authoring and health authority questions</li><li>Support the delivery of the technical documentation package to support product validation including validation and verification plans, technical reports / protocols, regulatory filings, and PAI readiness documentation</li><li>Lead the CPV strategy for the site, ensuring CPV and PPR programs are aligned to regulatory expectations and provide value to the business</li><li>Drive innovation, digital tool implementation, and continuous improvement for PLM approaches, utilizing CoPs and industry forums to stay current on regulatory guidance and industry trends</li><li>Develop and provide training for MSAT team members on PLM / PV concepts</li></ul>Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: <ul><li>Bachelors with a minimum of 8 years OR a Masters (MS) degree with a minimum of 5 years OR PhD with minimum of 3 years of post-graduate experience in the biopharmaceutical or pharmaceutical industry</li><li>Experience in biopharmaceutical or vaccines technologies, research & development and/or manufacturing</li></ul> Preferred Qualifications: If you have the following characteristics, it would be a plus:<ul><li>Experience in biopharmaceutical technologies and/or manufacturing with a strong technical understanding of process validation, process development, technology transfer, and product lifecycle management. Strong understanding of bioprocesses for drug substance (upstream and downstream)</li><li>Demonstrated skillset in CMC, including complex regulatory submission and response with a variety of regulatory agencies (FDA, EMA, JP, China etc.)</li><li>Understanding of GMP principles, regulatory submissions, and appropriate regulatory guidance</li><li>Strong verbal and written communication skills. Ability to interact with and influence across the entire MSAT organization</li><li>Strong executive presence and executive presentation skills</li><li>Able to interact well with peers, subordinates, and senior personnel in scientific, quality, engineering and operational disciplines. Embraces a team-based culture</li><li>Demonstrates initiative to solve problems and challenge status quo</li></ul>This role is on-site, offering opportunities to engage directly with teams and processes to make a tangible impact. #LI-GSK Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

MSAT Product Owner Associate Director

Site Name: USA - Pennsylvania - King of Prussia Posted Date: Sep 25 2025 At GSK, 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. We are looking to hire a MSAT Standards and Contamination Control Associate Director to join the Manufacturing Science and Technology (MSAT) organization in Upper Merion. This is a site-based team, providing technical support to ensure Upper Merion Biopharm site goals and objectives areachieved. The primary objective role of MSAT is to ensure manufacturing processes are capable, compliant and productive while ensuring product quality. The site MSAT team is also responsible for delivering continuous improvements to the existing supply chains supported by UM Biopharm and working with global MSAT to execute technology transfers a nd implement process-related improvement programs across the product lifecycle. In this role, you will lead a team to develop technical standards and processes, in alignment with central teams in topics including contamination control, single-use systems, lifecycle management, cleaning validation, leachables and extractables, and cell banking. This individual and their team are expected to become subject matter experts to provide in-depth technical support to resolve challenges, implement best practices, and support process improvements. The individual will also lead cell bank management at Upper Merion, supporting the inventory management, transfer, and technical oversight of the Upper Merion cell bank portfolio. The MSAT Standards and Contamination Control Associate Director will also be expected to develop systems and processes to develop a technical capable, motivated, and energized MSAT team. You will be accountable supporting technical and leadership capability development, with a focus on the future skills the MSAT team will be to develop to be successful and solve complex technical issues. You will be expected to manage within a matrix team, collaborating with team members from other UM Biopharm departments and with stakeholders global MSAT. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: <ul><li>Lead a team of technical experts across key disciplines including contamination control, single-use systems, cleaning validation, lifecycle management, leachables and extractables, and cell banking. In alignment with global MSAT, develop and maintain the technical standards in these areas for Upper Merion</li><li>Serve as a technical enterprise leader across the Upper Merion site, to support investigations, global initiatives, risk assessments, technology transfers, and regulatory / audit across these key areas of responsibility</li><li>In alignment with global MSAT, define the approach and strategy for the team, including staying current on industry trends and best practices</li><li>Manage the Upper Merion cell bank portfolio and key cell bank activities and documentation</li><li>Manages relationships with key internal (i.e. production, engineering, quality) and global teams, including a strong partnership with global MSAT technical standards team</li></ul>Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: <ul><li> Bachelors with a minimum of 8 years OR a Masters (MS) degree with a minimum of 5 years OR PhD with minimum of 3 years of post-graduate experience in the biopharmaceutical or pharmaceutical industry </li><li> Experience in biopharmaceutical or vaccines technologies, research & development and/or manufacturing </li></ul> Preferred Qualifications: If you have the following characteristics, it would be a plus:<ul><li>Experience in biopharmaceutical technologies and/or manufacturing with a strong technical understanding of bioprocesses for drug substance (upstream and downstream, including large scale cell culture bioprocessing and biopseparations and purification technologies</li><li>Deep understanding of current trends in the industry, ICH guidelines, and GMP principles, particularly in the fields of contamination control, single-use systems, and process validation</li><li>Understanding of process validation, process development, technology transfer, and product lifecycle management</li><li>Strong interpersonal and leadership skills to manage cross-functional teams. Ability to influence cross-functionally and drive improvements</li><li>Strong verbal and written communication skills particularly in the area of technical and regulatory related matters</li></ul>This role is on-site, offering opportunities to engage directly with teams and processes to make a tangible impact. #LI-GSK Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

MSAT Standards and Contamination Control Associate Director

Site Name: USA - Pennsylvania - Upper Providence, USA - Massachusetts - Waltham Posted Date: Sep 26 2025 Are you driven by the opportunity to lead clinical and scientific strategies for advanced-stage assets in immunology and fibrosis, shaping the future of treatments for complex diseases? If so, the Senior Medical Director, Clinical Development - Rheumatology/Immunology role could be an exciting opportunity to explore. GSK seeks a Senior Medical Director, Clinical Development to provide clinical and scientific leadership for potential new, established, and emerging indications for advanced stage assets in the immunology and fibrosis portfolio. The Senior Medical Director, Clinical Development will work with medicine teams to plan and assure delivery of clinical research and development activities. As well as working with early development teams to plan clinical development programs and establish efficient collaboration enabling seamless transition from early to late phase of development. PLEASE NOTE: This career opportunity requires an on-site office presence (minimum of two days a week) at one of GSK's US (Upper Providence, PA or Waltham, MA) sites. Key Responsibilities:<ul><li>Lead the end-to-end clinical development strategy for a drug or program. Manage specific clinical development plans for product(s) and/or indication(s) in specific therapy/disease areas.</li></ul><ul><li>Oversee Integrated Evidence Plan (IEP), Clinical Development Plan (CDP) and its component clinical trials; be accountable for clinical aspects of Target Medicine Profile (TMP).</li></ul><ul><li>Provide strategic leadership, for example in assuring that the clinical study designs are aligned with the IEP and CDP, and consider the scientific rationale, regulatory requirements, product development plan and commercial goals</li></ul><ul><li>Establish and deliver clinical development timelines, enabling key decision points and Go/No Go criteria for the CDP</li><li>Collaborate with internal teams (Commercial, Research, Regulatory, Clinical Operations, Statistics etc.) and act as the clinical point of contact for senior management.</li><li>Contribute to the strategic and organizational initiatives in Clinical Development, along with Business Development activities, including due diligence projects</li><li>Build and manage external relationships with a range of scientific external experts to align clinical programs with business strategy and patient needs.</li><li>Assess and mitigate risks, evaluate technical success probabilities, and identify transformational opportunities with significant patient benefits.</li><li>Contribute to global regulatory submissions and interactions, including briefing documents and responses.</li></ul><ul><li>Champion implementation of innovative methods and processes within clinical development and gain stakeholder support; encourages others to think differently and produce business solutions</li></ul>#LI-GSK Basic Qualifications:<ul><li>Medical degree and clinical medical specialty board qualification in Rheumatology or Allergy/Immunology. </li><li>Experience in (bio-)pharmaceutical industry with experience in Rheumatology or Immunology clinical drug development.</li><li>Experience with planning clinical development for a Rheumatology or Immunology asset and/or indication.</li><li>Experience in drug development, including Phase 2 and Phase 3 clinical trial design, initiation, execution, and closure. </li><li>Experience of global regulatory filings/submission.</li><li>Experience of immunologic-mediated diseases, underlying biology, and potential therapeutic targets.</li></ul>Preferred Qualifications: <ul><li>Deep experience in Rheumatology, Autoimmune, or the Neuroinflammation space.</li><li>Solid understanding of needs and priorities of regulators, payers, and prescribers in relevant global market(s).</li><li>Experience collaborating with multiple stakeholders on complex projects.</li><li>Record of building and maintaining strong relationships with internal and external stakeholders.</li></ul> Please visit GSK US Benefits Summary 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Senior Medical Director, Clinical Development - Rheumatology/Immunology

Site Name: USA - Pennsylvania - King of Prussia Posted Date: Sep 25 2025 At GSK, 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. We are looking to hire a MSAT Data Science and Analytics Associate Director to join the Manufacturing Science and Technology (MSAT) organization in Upper Merion. This is a site-based technical team responsible for ensuring manufacturing processes are capable, compliant and productive while maintaining product quality. The site MSAT team is also responsible for delivering continuous improvements to the existing supply chains supported by UM Biopharm and working with global MSAT to execute technology transfers and implement process-related improvement programs across the product lifecycle. The Upper Merion MSAT team is also accountable for delivering data science and analytics solutions to improve business outcomes. The MSAT Data Science and Analytics Associate Director will lead a team of data scientists and engineers to leverage data science and data analytics to provide business insights and solve complex technical and business problems. The team will leverage data as a key asset to accelerate technology transfer and CMC, drive continuous improvement in key business processes, reduce waste, and enhance knowledge management across the site. The team will coordinate with R&D colleagues engaged in technology transfer, manufacturing and technology groups involved in monitoring (CPV), comparability, and investigations, analytical teams involved in product, release, and stability testing, quality teams engaged in managing quality systems and quality data, and engineering groups responsible for process control, reliability, and robustness to build informatics solutions that meet the desired customer needs and user experiences. The team will develop and deploy novel digital models, tools, and visualizations and be responsible for maintaining site databases, models, and infrastructure. The MSAT Data Science and Analytics Associate Director will be expected to support technical development their organization, developing high performing data scientists and engineers. You will also be expected to manage within a matrix team to ensure key data and analytics needs are met across the site (i.e. production, quality, engineering) and to collaborate with stakeholders in global MSAT, tech, and R&D to drive implementation of novel data analytics tools and technologies into the commercial manufacturing space. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: <ul><li>Serve as the leader for data science and analytics capabilities at Upper Merion. Accountable for development and deployment of the strategic data and analytics plan for the Upper Merion site, in collaboration with central digital and analytics teams, to meet the customer needs.</li><li>Leverage digital tools and solutions to drive business value and continuous improvement in technical or site systems and processes, including CMC (new product introduction and regulatory filing), technical (process monitoring and CPV, comparability, and investigations), site sustainability, manufacturing plant (engineering) performance and reliability, quality control release and stability date, and quality systems and data.</li><li>Maintain key site-based digital infrastructure, including models, databases, and software.</li><li>Lead a team of scientists and engineers to work collaboratively and efficiently to deliver the digital objectives. Support capability development of the MSAT team to learn/implement new analytical technologies and modeling systems.</li><li>Manages relationships with key internal (i.e. production, engineering, quality) and external (i.e. global MSAT team, IT, Tech, R&D) partners to deliver technical objectives and implementation of novel data and analytics platforms and technologies.</li></ul>Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: <ul><li>Bachelors with a minimum of 8 years OR a Masters (MS) degree with a minimum of 5 years OR PhD with minimum of 3 years of post-graduate experience in data engineering, data science, computer science field or equivalent. </li><li>Experience in biopharmaceutical or vaccines technologies, research & development and/or manufacturing.</li><li> Experience in digital, data, and analytics techniques in the pharmaceutical or biopharmaceutical industry. </li></ul> Preferred Qualifications: If you have the following characteristics, it would be a plus:<ul><li>In-depth experience with digital, data, and analytics techniques in the pharamaceutical industry. Familiarity and experience with relational databases, statistical softwares (i.e. SAS, SIMCA, JMP or WebStatistica), modeling and visualization softwares (i.e. Python, R, Matlab, , SQL, MS Power). Experience of developing or applying techniques such as pre-processing, classification, regression, clustering, dimensionality reduction and model selection.</li><li>Experience with development and maintenance of digital infrastructure, including cloud architecture.</li><li>Experience with manufacturing / engineering environments including systems such as IP-21, M-ERP, LIMS, Aspen eBRs, is preferred.</li><li>Experience with industrialization or implementation of models in a GMP environment, including awareness of recent industry trends and requirements as they relate to data science or data validation.</li><li>Ability to identify and solve complex, technical problems with pace based on business needs and priorities.</li><li>Strong interpersonal and leadership skills to manage a technical team and cross-functional teams. Embraces a team-based culture.</li><li>Strong verbal and written communication skills. Able to present data science / statistical methods to non-statistical team members.</li></ul>This role is on-site, offering opportunities to engage directly with teams and processes to make a tangible impact. #LI-GSK Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

MSAT Data Science and Analytics Associate Director

Site Name: USA - Pennsylvania - Upper Providence, GSK HQ, Switzerland - Zug Posted Date: Sep 25 2025 As a Global Marketing Director, you will translate our science into commercial success throughout the product lifecycle by ensuring you drive competitive product profiles and build long-term brand value through working in partnership with the cross functional medicines development team. You will lead the development of insight-driven global product strategies and plans, deliver ambitious long-range forecasts, enable outstanding launches, and ensure excellent customer experience in partnership with co-create markets through creating omnichannel content. In this role you'll develop and stretch to be the best in the industry across key Global Strategy and Enterprise Leadership Capabilities. Within GSK's Pharmaceuticals business, you are expected to generate long-term value for GSK and ultimately improve the lives of patients around the world. You will produce exquisite insight, develop clear, competitive global brand strategies and plans, enable outstanding launches, and focused implementations in partnership with co-create markets. You will be responsible for: Driving and managing the business <ul><li>Accountable to develop brand strategy and deliver launch/brand plan in accordance with Integrated Asset Plan (IAP) across customer segments including Patient, HCP and Payer, in partnership with key cross functional partners and LOCs enabling core LOCs to execute the strategy and achieve the agreed sales ambition.</li><li>Understand, value, and prioritize sources of differentiation by leveraging cross functional insights, elucidating implications of emerging data and competitive launches across cross functional teams and strategies</li><li>Develop strategic choices (positioning, segmentation, targeting, etc.) and promotional strategies for the asset</li><li>Partner with Insights to deliver Global Forecast aligned to strategy, generating recommended assumptions and strategic input</li><li>Elucidate required SG&A and commercial model to optimize asset performance in Global markets</li><li>Lead lifecycle management strategy to drive additional value for the asset, launch sequence strategy, optimizing approaches to market</li><li>Lead RFP/Pitch and agency selection for the brand's Agency of Record (AOR). Onboard and then manage Agency of Record and key projects related to development of the global brand (customer journey, personas, brand visual identity, value proposition, messaging, and campaign development) in collaboration with co-creation markets and via MOC </li><li>Drive LOC engagement strategy and lead development and management of global commercial budget and input into LOC operational planning</li><li>Drive culture of trust, respect, transparency, and accountability</li></ul>Managing corporate reputation & building trust<ul><li>Build strong cross business unit/functional relationships, to maximize synergies and make sure that GSK has unified, coherent and trusted representation externally.</li><li>Shaping the external environment in-line with LOC strategy</li></ul>Why You? Basic Qualifications:<ul><li>Bachelor's degree</li><li>5+ years of marketing experience in the pharmaceutical industry, specifically in oncology.</li><li>3+ years of experience in the US market or a Tier 1 market.</li><li>Requirement of 2 -3 days per week in the office.</li></ul>Preferred Qualifications:<ul><li>Senior marketing experience in the US or tier 1 market with multiple launch experiences.</li><li>Recent launch experience at global/ regional or LOC level and experience working across global to local (or vice versa).</li><li>Led development of brand imagery, insights, segmentation, core campaigns as well as co-create experience.</li><li>Experience of leading medicines at different stages of their life cycle like early assets, work with R&D or consulting experience or late-stage assets.</li></ul>#LI-GSK Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Global Marketing Director, Oncology

Site Name: USA - Pennsylvania - Upper Providence Posted Date: Sep 23 2025 The Principal Engineer of Connectivity Service Management is a senior technical leader responsible for ensuring the stability, performance, and security of GSK's global network infrastructure. This role involves leading complex network projects, providing expert-level troubleshooting, and guiding the Network Operations team in best practices and advanced network solutions. Your responsibilities include... <ul><li>Serve as the technical authority for network operations, providing guidance on complex network issues and solutions.</li><li>Support and provide feedback in the design, implementation, and maintenance of high-performance, resilient network infrastructures.</li><li>Mentor and develop network engineers, fostering a culture of continuous learning and technical excellence.</li><li>Oversee the day-to-day operations of GSK's global network, ensuring optimal performance and availability.</li><li>Conduct advanced troubleshooting and root cause analysis of network incidents and problems.</li><li>Aid in the continual improvement of network management and monitoring tools to ensure proactive identification and resolution of issues.</li><li>Maintain robust network security measures to protect against threats and vulnerabilities.</li><li>Ensure network operations comply with relevant security policies, standards, and regulatory requirements.</li><li>Conduct regular security assessments, audits, and penetration tests, addressing any identified risks.</li><li>Stay current with emerging network technologies and industry trends, recommending and implementing innovative solutions.</li><li>Drive continuous improvement initiatives to enhance network performance, reliability, and security.</li><li>Develop and enforce network policies, procedures, and best practices.</li><li>Manage relationships with network service providers, hardware vendors, and other external partners.</li><li>Collaborate with business units, IT teams, and stakeholders to understand and meet network requirements.</li><li>Communicate network performance, issues, and initiatives to stakeholders at various levels of the organization.</li></ul>Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: <ul><li>Bachelor's degree in computer science, Information Technology, or a related field. Master's degree preferred.</li><li>10+ years of experience in network engineering and operations, 5+ years in a senior or lead role.</li><li>Knowledge of network infrastructure, protocols, and technologies, including Cisco, Juniper, Palo Alto, and others.</li><li>Experience in network security principles and practices.</li><li>Experience with network design, implementation, and troubleshooting</li></ul>Preferred Qualifications: If you have the following characteristics, it would be a plus: <ul><li>Five years of experience in the pharmaceutical industry, with a solid understanding of its technological trends.</li><li>Excellent leadership, communication, and interpersonal skills.</li><li>Strong analytical and problem-solving abilities.</li><li>Ability to work effectively in a fast-paced, dynamic environment.</li><li>Passionate about enhancing the customer experience.</li><li>Experienced in initiating and delivering large-scale operational programs.</li><li>Skilled in operating systems and database administration.</li><li>Proficient in agile delivery methodologies.</li><li>Experienced in the DevOps operational model.</li></ul>#Li-GSK Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Ops/SRE -Principal Engineer

Site Name: USA - Maryland - Rockville Posted Date: Sep 23 2025 Are you looking for an opportunity to lead and inspire Site Quality teams toward the pursuit of operational excellence in manufacturing practices while building a high-performance network? If so, this is the role for you. As Site Quality Lead Director, you will provide strategic leadership and direction for the site's Quality function, ensuring the highest standards of product quality and compliance with GSK corporate policies and regulatory standards. The role is accountable for the quality of all products released from the site and for representing GSK in health authority interactions. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following :<ul><li>Strategy Deployment: Serve as a member of the site leadership team, actively contributing to strategy deployment to support GSK objectives.</li><li>Quality and Compliance Strategies: Develop and implement quality and compliance strategies and initiatives, ensuring full deployment of GSK's Quality Management System (QMS).</li><li>Continuous Improvement Culture: Foster a culture of continuous improvement, developing and monitoring key quality metrics to drive performance.</li><li>Quality Leadership: Provide leadership and direction in all Quality related matters, ensuring operational business compliance with cGMP and regulatory requirements.</li><li>Team Development: Lead and develop the Quality organization on site, making decisions that prioritize patient safety and product quality.</li><li>Strategic Quality Planning: Develop and execute a long-term quality strategy that aligns with the overall business objectives, ensuring that quality considerations are integrated into the site's strategic planning and decision-making processes.</li><li>Regulatory Compliance: Maintain a state of inspection readiness by staying abreast of regulatory changes and trends, and ensuring that the site's quality systems and processes are robust and compliant with current industry standards and practices.</li><li>Quality Culture and Employee Development: Champion a strong quality culture throughout the site by promoting quality awareness, accountability, and continuous improvement. Develop and mentor quality personnel to build a pipeline of talented quality professionals capable of supporting the site's current and future needs.</li></ul>Leadership Competencies:<ul><li>Patient Focus: Lead with a patient-centric approach in all quality-related decisions and actions.</li><li>Integrity: Uphold the highest ethical standards, ensuring transparency and honesty in all operations.</li><li>Respect for People: Foster an inclusive environment that values diversity and encourages collaboration and innovation.</li><li>Do the right thing: Demonstrate the courage to make tough decisions and challenge the status quo in the best interest of patients and the company.</li></ul>Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals:<ul><li>Bachelor's Degree with 10 plus years of experience in pharmaceutical OR biological production environments</li><li>Experiencewith FDA/EU/ICH/CDN/AUS guidelines</li><li>Leading First & Second Line Managers</li><li>Experience working with Site Leadership Team</li><li>Experience with patient safety and product quality</li></ul> Preferred Qualifications: If you have the following characteristics, it would be a plus:<ul><li>Experience in leading cross-functional teams and driving organizational change</li><li>Excellent interpersonal and communication skills, with the ability to engage effectively with stakeholders at all levels</li><li>Strong knowledge of good manufacturing practices and data integrity</li><li>Demonstrated ability to challenge the status quo and drive continuous improvement</li><li>Ability to make risk-based and autonomous decisions</li></ul>This position is located onsite in Rockville, MD. #LI-GSK The annual base salary for new hires in this position ranges from $201,300 to $335,500 taking 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. Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Site Quality Director

Site Name: Upper Merion Posted Date: Sep 23 2025 GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centered on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems. Our diverse portfolio consists of vaccines, specialty medicines, and general medicines. Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges. This role is an exciting opportunity to lead procurement activities at one of our U.S. sites. You'll work closely with cross-functional teams to ensure the site has the goods and services needed to operate efficiently. We value candidates who are proactive, collaborative, and passionate about driving value while maintaining strong supplier relationships. Responsibilities - Develop and execute procurement strategies to meet site needs and align with company goals. - Manage supplier relationships to ensure quality, cost-effectiveness, and timely delivery. - Collaborate with site teams to understand requirements and provide procurement solutions. - Monitor and report on procurement performance, identifying opportunities for improvement. - Ensure compliance with company policies and regulatory requirements. - Support sustainability initiatives by sourcing responsibly and reducing environmental impact. Basic Qualifications: - Bachelor's degree in business, supply chain, or a related field. - 5+ years of procurement experience, preferably in a manufacturing or operations environment. - Experience analyzing data and making informed decisions. - Experience using procurement systems and tools - Must be able to work on-site at the designated location 2-3 days per week. Preferred Qualifications: - Master's degree or professional certification in procurement or supply chain (e.g., CPSM, CIPS). - Experience in the pharmaceutical or healthcare industry. - Knowledge of sustainability practices in procurement. - Proven track record of delivering cost savings and process improvements. - Familiarity with ERP systems like SAP or Oracle. #LI-GSK Please visit GSK US Benefits Summary t o 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. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. 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