Software Engineer

• Design and implement technical solutions aligned with platform strategy.
• Support platform design and deployment, ensuring harmonization and quality across sites.
• Co-develop secondary processes and provide technical expertise during process transfers from R&D to manufacturing.
• Define strategies for new equipment and technologies, including benchmarking and validation.
• Coordinate technical expertise networks and foster knowledge sharing internally and externally.
• Lead or contribute to transversal projects and multidisciplinary workstreams.
• Provide troubleshooting support and manage knowledge systems for future process ownership.

Manager – Aseptic Process Engineering

Solutions Engineer

• Design, build and improve data integration and delivery solutions between automation systems and analytics platforms.
• Own technical implementation and maintenance of industrial data platforms, ensuring performance and availability.
• Define and apply data handling standards for storage, tagging and archival to protect data integrity and accessibility.
• Work with cross-functional teams to support system lifecycle activities: specification, commissioning, validation, and handover.
• Provide coaching, training and guidance to automation technicians and engineers on data connectivity and best practices.
• Assess system performance and recommend hardware, software or architecture improvements.
• Engagement with and periodic travel to sites within the global supply chain.

Automation Data Integration Engineer

Sales

• Lead your team in the development of performance driving key account plans
• Embed an omni-channel approach to engaging with customers
• Develop strong relationships with cross-functional partners to execute the strategic brand plan
• Drive a culture of leadership, sales excellence and continuous improvement
• Keep up to speed on developments in the respective therapeutic areas
• Build strong relationships with cross-functional partners; regulatory, medical, and market access

National Sales Manager – Biologics

Marketing

• Provide input to the strategic and operational business plan, develop and deliver global marketing campaigns built on key customer/consumer, competitive insights, ensuring full engagement with co create countries.
• Drive/support best-in-class launch readiness across all Geo Expansion LOCs
• Partner with key LOCs to ensure the global to local utilization rates are at the required standards, and campaigns are analyzed and track for quick course correction if needed.
• Have strong awareness and understanding of how to leverage promotional channels to support the desired business outcome in support of LOC decisions making.
• Work with Agency of record management/interactions for strategic and promotional initiatives that support brand strategy.
• Collaborate with the analytics Team to further develop data driven activities.
• Facilitate best practice sharing and implement key insights and course correction plan from different markets based on campaign insights/metrics.
• Present campaign progress as needed to Matrix colleagues and other relevant bodies for awareness and/or approvals.
• Perform risk management assessment identifying potential risks for the performance and trust pillars where required ensure impactful mitigation in place.
• Responsible for budget management ensuring clear overview of spend allotment and maximization of resources.

Global Marketing Manager – HCP, Vaccines

Director

• Lead the deployment and performance management processes in R&D DDS for Change Control, Deviation, CAPA, Risk Management, Management Monitoring, Quality Council and GMP training
• Responsible for leading a team that is accountable for deploying the standardized GSK quality business processes in R&D Quality and DDS, analyzing & interpreting quality system metrics and acting on the data analytics to propose process improvements and efficiencies to GBPOs
• Responsible for developing strong partnerships across R&D Quality and DDS Operational teams to ensure that compliance risks are appropriately identified, escalated, and mitigated
• Provide leadership and management of R&D SOPs associated with the quality processes to ensure the creation, implementation, and maintenance of harmonized and efficient procedures
• Ensure the continuous alignment of, compliance to, and effectiveness of R&D processes within the QMS framework and where assigned, provide capability build for R&D QMS content owners, QMS Champions and Local SMEs on phase appropriate QMS implementation
• Responsible for managing the materials required for quality council and engaging with key stakeholders across the company to prioritize support and risk mitigation
• Accountable for the content and alignment of the R&D QMS to the legislation, and supporting Pilot Plants during inspections and issue resolution
• Providing support for change management and capability build for the Pilot Plants and aligned SMEs related to our quality processes
• Supports and drives rapid resolution of technical issues escalated from R&D Quality and DDS teams which have a direct connection to one of our quality processes
• Works with Global and Regional / Local Regulatory to understand, translate and apply local regulations, being conversant with statutory obligations and GSK procedures for all regulatory requirements to enterprise quality processes
• Motivate, focus and develop the team of quality process owners, driving continuous improvement and inclusivity to ensure operational excellence

Quality Process and Data Director

Project Manager

• Manage a team of 6-8 Medical Project Managers supporting oncology early, late and launching assets.
• Establish clear performance expectations in collaboration with business partners.
• Monitor performance progress and track delivery against annual goals.
• Cultivate a culture of executional excellence by maintaining high standards in planning, delivery, and effective stakeholder management.
• Engage in Project Management Leadership Team meetings, collaborating to shape central team strategic priorities.
• Support capability-building initiatives by ensuring implementation of best practices across therapies.
• Drive operational excellence using project management tools and implementing performance dashboards.

Medical Project Management Director, Global Oncology

• Define and implement the vision and strategy to translate Quality standards into innovative, compliant, and efficient R&D Quality processes that drive operational excellence and value creation.
• Oversee, and optimize core Quality Processes, including Documentation, Change Control, Deviation, CAPA, GMP Training, phase appropriate QMS implementation, Quality Council, Data Management.
• Accountable for ensuring robust, simple and standardized quality processes, change management and deployment across R&D, including implementing digital data enhancements and foundations.
• Ensure quality management for validation and qualification of equipment, facilities and computerized systems in alignment with regulatory and company global requirements.
• Drive digital transformation initiatives, leveraging GPS principles to improve systems, governance, data analytics, and reporting capabilities.
• Establish and monitor key performance indicators (KPIs) for Quality Systems and Processes to ensure effective quality governance and continuous improvement across operations.
• Foster a culture of learning and capability development by sponsoring initiatives such as Learning Zone, Training Academy, and Competency-Based Learning models.
• Lead the development of the Quality R&D QS&D team by enhancing skills and competencies, managing individual and team performance, and fostering behaviors aligned with GSK’s culture and leadership expectations.
• Drive data management excellence, by promoting a culture of accountability through governance, training and awareness initiatives.
• Provide strategic guidance to ensure data-related projects uphold ALCOA principles and aligned with organizational objectives.
• Provide support during regulatory inspections, global audits, and internal audits, conduct site operations oversight through GEMBA walks or other effective methods to ensure compliance and operational excellence.

Senior Director, Quality Systems and Data

Program Manager

• Embed Agile Project Management Practices: Steer cross-functional project teams through all phases of agile software development lifecycle (SDLC);
• Enhance Team & Project Effectiveness: Collaborate with team leads to identify and address challenges hindering team and project performance;
• Drive Cross-Team Coordination & Collaboration: Deploy interventions that contribute to single view of each project and seamless integration of deliverables;
• Build Stakeholders & Partner Relationships: Work alongside engineering leads, Product Managers, and Quality Managers to implement project discipline across deliverables;
• Reduce Risk & Dependency Impact: Embed practices that enable risk and dependency identification, assessment, documentation, and monitoring;
• Measure Impact with Data & Insights: Contribute to establishing measurable objectives and key results (OKRs);
• Proactively Address Change: Integrate change management activities into project plans;

Program Manager II

Manager

• Create, update and review medical information content that is scientifically balanced, concise and evidence-based for healthcare and payer audiences.
• Maintain and improve the medical information database and launch readiness plans for assigned therapeutic areas.
• Provide clinical and scientific expertise for payer-directed materials and support payer engagement needs.
• Review and provide medical sign-off for promotional and scientific materials to ensure compliance with standards and regulations.
• Collaborate with cross-functional teams to produce reactive and proactive scientific presentations and responses for healthcare professionals.
• Share medical insights and contribute to continuous improvement of medical information practices and workstreams.

Medical Information Manager

• Own multiple National Commercial and Medicare Pharmacy Benefit Manager (PBM) contracts, serving as the expert on contract terms and conditions.
• Frequently collaborate with the Account Team, Contract Analytics, and Contract Operations to inform on contact language, share insights regarding stakeholder implications of contracting strategies, understand and implement contract changes, and ensure operational feasibility.
• Draft, review & redline contract language and rebate agreements.
• Interface directly with Zinc Health / CVS Caremark regarding contract negotiations and bid submissions.
• Mitigate revenue leakage through completing rebate payment reviews and approvals and initiating approval escalation.
• Understand Anti-Bribery & Corruption (ABAC), other GSK policies, and relevant pharmaceutical laws and regulations to ensure appropriate language is incorporated in relevant contracts to minimize legal, financial, operational and reputational risk to GSK.
• Partner with Legal on contract language updates.
• Ensure contract documentation is stored and properly organized in the required repositories in a timely manner.
• Partner with Business Risk and Compliance to support internal and external audits and to ensure risks are effectively monitored.
• Build and foster relationships with many cross-functional teams.
• Communicate key status updates to leadership and other stakeholders in a timely manner.
• Manage special projects to improve efficiency and effectiveness, simplify, and meet customer needs.
• Provide ad hoc support to leadership.

Contract Development Manager

• Responsible for the development and execution of the account plan for targeted accounts
• Generate a top down and bottom-up organization approach that leads to the achievement of all leading and lagging performance indicators across all functions.
• Demonstrate executive presentation skills and strong ability to interact with both C and D Suite within accounts.
• Demonstrate ability to lead matrix teams to deliver organizational impact.
• Ability to synthesize data into tailored engagement’s that forges on-going strategic partnerships.
• Improves ViiV’s reputation in the market through connecting multiple market stakeholders together for improved patient outcomes.
• Responsible for the coordination of executive exchanges that lead to success for both organizations.
• Achievement of product adoption goals for the ViiV portfolio
• Removal of non-clinical barriers resulting of faster adoption of ViiV products across the account.
• Local leader that drives a high accountability environment and achievement of ways or working goals.
• Aligning to and exemplifying ViiV’s core values with every interaction, both internal and external.

Director, Strategic Accounts, Central West

Designer

• Provide expertise in DNA cloning, in-vitro RNA transcription and cell-based assay characterization of RNA vaccine candidates
• Design and develop new assays and technologies to support RNA vaccine generation and evaluation
• Collaborate with cross-functional teams to support the translation of research findings into vaccine development
• Stay updated with the latest scientific advancements in the field of RNA vaccines
• Assist in the preparation of research findings for internal reports and publication in scientific journals
• Ensure compliance with all regulatory standards in the development and testing of RNA vaccines
• Contribute to a culture of teamwork and scientific excellence

Scientist, RNA Design and Biology

Community Manager

• Lead the execution of oncology portfolio strategy aligned to community oncology and specialty GPO networks.
• Translate customer insights and analytics into practical account plans and measurable KPIs.
• Coordinate cross-functional execution with Brand, Market Access, Medical Affairs, Field, and Commercial Operations.
• Guide pilots and test-and-learn initiatives to optimize account engagement and measure outcomes.
• Build senior stakeholder alignment and present account performance and recommendations to leaders.
• Support the development of team members and partners to strengthen account capabilities and ways of working.

Strategy Director – Community Oncology

• Lead statistical planning and delivery across clinical programs and contribute to clinical developments plans within oncology.
• Work closely with clinical, regulatory, safety, data science and commercial teams.
• Design robust clinical trials and analyses that shape development decisions and regulatory strategy.
• Drive methodological innovation and mentor colleagues.

Statistics Leader – Oncology Statistics

• Design and oversee interventional clinical studies, ensuring alignment with strategic objectives and evidence plans.
• Provide scientific oversight for study protocols, analysis plans, and interpretation of study data.
• Ensure patient safety and scientific integrity throughout study conduct, including medical governance and monitoring.
• Collaborate with cross-functional teams to ensure seamless execution and delivery of clinical programs.
• Prepare and present study results for scientific meetings, publications, and regulatory submissions.
• Engage with internal and external stakeholders, including investigators and thought leaders, to enhance study design and execution.