Jobs at GSK

Lead commercial growth and customer engagement across an assigned territory in India. Build relationships with healthcare professionals and institutional stakeholders, create territory business plans, conduct professional and educational visits, gather market insights, collaborate cross-functionally, and ensure compliance with company policies and regulations.

Lead commercial growth and customer engagement across Jaipur by building relationships with doctors, hospitals and pharmacists; create and execute territory business plans; conduct field visits and professional meetings; capture market and customer insights to improve performance; collaborate with commercial, medical and access teams; and record activities accurately using company systems while following local regulations.

This 12-month full-time internship offers university students the chance to work in Marketing at GSK, contributing to projects while gaining valuable experience.

Lead statistical strategy and execution for oncology clinical development across phases. Design and analyze trials using simulation, Bayesian and real-world data approaches; author protocols/SAPs; deliver timely, high-quality statistical outputs; influence asset and regulatory strategy; represent biostatistics externally and mentor project teams.

Le champion de l’amélioration continue dirige des initiatives Lean Six Sigma et d’excellence opérationnelle dans un environnement biopharmaceutique manufacturier. Il identifie les occasions d’amélioration, facilite les projets Kaizen et DMAIC, mobilise les équipes, soutient la résolution des problèmes et assure la durabilité des gains. Le poste comprend également des responsabilités liées à la qualité, aux CAPA, aux audits, à la conformité GMP, à la gestion des risques et à la formation des employés.

Leads GSK’s Northeast oncology sales region, translating enterprise and brand strategy into regional execution plans. Oversees sales performance, marketplace acceleration, account pull-through, business planning, launch acceleration, compliance, and talent development. Partners cross-functionally with Marketing, Medical, Market Access, Patient Services, and Sales Operations. Requires strong oncology and pharmaceutical commercial expertise, strategic thinking, data-driven decision-making, and regular domestic travel across the assigned territory.

Leads AI and technology adoption across pharmaceutical R&D programs. Develops change and adoption plans, assesses readiness and risks, coordinates stakeholders, supports implementation of AI tools and data platforms, tracks adoption and value measures, and delivers focused transformation projects. The role translates technology changes into process, role, behavior, and capability improvements while building sustainable internal capability and influencing senior technical and business stakeholders.

Leads quantitative systems pharmacology modeling for drug discovery and development. Builds mechanistic disease and drug models, integrates complex biological data, evaluates disease mechanisms and treatment modalities, supports preclinical study design, and informs target prioritization and clinical translation. Collaborates with multidisciplinary research teams, validates modeling methodologies, interprets results, and applies emerging approaches such as AI, machine learning, omics integration, and agentic AI.

Leads enterprise AI and technology adoption across pharmaceutical R&D, connecting behavior and process change to measurable business value. Builds an internal adoption capability, establishes a hub-and-spoke operating model, develops adoption roadmaps and measurement frameworks, and partners with technology programs to improve delivery and sustained usage. The role influences senior scientific and technology leaders, coordinates cross-functional transformation initiatives, and balances strategic leadership with hands-on execution.

Coordinates GMP quality processes in SAP, manages Method of Analysis documents and SOPs, and oversees related training. Evaluates purchased materials, spare parts, suppliers, and contractors; makes quality release or rejection decisions; manages complaints, OOS events, deviations, third-party incidents, and CAPAs. Assesses supplier performance and coordinates site Product Quality Reviews. Requires a relevant scientific degree, approximately three years of pharmaceutical QA compliance experience, cGMP knowledge, fluent English, and Microsoft Office skills.

Leads smart manufacturing transformation across U.S. pharmaceutical and vaccine manufacturing sites. Responsibilities include identifying and prioritizing opportunities, developing Industry 4.0 roadmaps, delivering MES and OT/IT integration solutions, applying analytics and AI, leading cross-functional teams, establishing validation and cybersecurity standards, and tracking benefits through operational handover. Requires experience with regulated manufacturing, complex transformation programs, and deployment of data-driven manufacturing solutions.

Drive specialty pharmaceutical sales strategy across assigned territories and accounts. Build relationships with healthcare professionals, execute business plans and promotional campaigns, gather market insights, support new launches, coordinate demand planning, and collaborate with market access teams. Maintain customer segmentation, analyze market and competitive data, ensure product availability, and comply with company policies and regulations. The role requires specialty portfolio experience, key account management, healthcare knowledge, Arabic and English fluency, and approximately 50% travel to remote areas.

Leads strategic technology transformation across pharmaceutical R&D programs. Partners with senior scientific, technology, and business leaders to shape strategy, roadmaps, investment decisions, operating models, partnerships, and business cases. Evaluates program progress, risks, value delivery, and build-versus-buy choices while identifying reusable capabilities and removing barriers. Requires significant pharmaceutical R&D or biotechnology experience, strong drug research knowledge, strategic project leadership, structured analysis, and executive-level influencing skills.

Promotes GSK prescription medicines in Odesa by meeting healthcare professionals, organizing presentations and conferences, building long-term partnerships, expanding customer networks, executing territory visit and promotional plans, maintaining product and competitor knowledge, presenting products ethically, negotiating, and completing reporting responsibilities.

Leads quality control activities for new vaccine projects, including analytical method development, validation, verification, transfer, equipment qualification, and testing. Coordinates with global QC and MSAT teams, ensures GMP and regulatory compliance, prepares validation plans and documentation, manages project budgets, and supports the transition from project to routine QC operations. Also drives knowledge transfer, training, laboratory quality systems, investigations, and continuous improvement.

Intern will support the Drug Product Development Process Engineering team in developing, optimizing, and validating Electrical Impedance Cytometry methods for pharmaceutical nanoparticle characterization. Responsibilities include laboratory experiments, sample preparation, instrument operation, data analysis in Excel or similar tools, method documentation, scientific reporting, cross-functional collaboration, and adherence to laboratory safety, data integrity, and quality standards.

Leads learning and development across a biopharmaceutical manufacturing site. Responsibilities include designing training curricula and competency frameworks, managing onboarding and role-transition training, evaluating training effectiveness, analyzing proficiency data, improving learning processes, and introducing innovative training methods. The role collaborates across departments, supports compliance, and leads training initiatives for employees at different job grades.

Two-year graduate program focused on pharmaceutical quality science and manufacturing. Participants rotate through quality laboratories and production facilities, gaining experience in analytical testing, quality systems, deviations, CAPA, change control, compliance, risk management, sustainability, and continuous improvement. The role involves cross-functional collaboration with manufacturing, quality, technical services, R&D, and supply chain teams while developing digital analytics and problem-solving skills.

Lead field sales for adult vaccines across Changhua by building relationships with healthcare professionals and public health partners. Provide evidence-based education, develop territory plans, use customer insights and data to improve patient access, collaborate cross-functionally on local initiatives, and maintain compliant CRM and budget records. The role is on-site, field-based, and requires regular territory travel.

Supports pharmaceutical product launches, technology transfers, lifecycle changes, and site impact assessments. Acts as a subject matter expert for manufacturing, packaging, equipment, systems, process optimization, validation, troubleshooting, material master data, and M-ERP maintenance. Coordinates cross-functional projects, supports GMP/GDP compliance and audits, investigates root causes, improves processes, and minimizes write-offs. Requires at least five years of pharmaceutical industry experience, scientific education, strong technical and project skills, and fluency in Japanese and English.