Project Manager, Data Science Manager, Operations Manager

Overview

Site Name: USA - Pennsylvania - Marietta
Posted Date: Feb 4 2026
Job Title: Project Manager

Business Introduction:
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is vital to bringing our innovations to patients quickly, efficiently and effectively.

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 smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.

Position Summary: You will lead projects that improve how we work and how we serve customers. You will plan, deliver and close projects on time, on budget and to agreed quality. You will work with teams across functions and with external partners. We value people who are organized, clear communicators, and who solve problems with practical, simple solutions. This role offers strong growth, visible impact and the chance to contribute to our mission of uniting science, technology and talent to get ahead of disease together.

• Define and determine project scope (In-and out-of-scope), charter, areas of responsibilities, and identify stakeholders in collaboration with GSK Marietta and/or global resources.
• Demonstrated familiarity and compliance with cGMP's, EHS procedures and regulations, facility regulatory guidelines, and standard operating procedures.
• Decide project resource requirements and resourcing strategy for project team as well as recruit team. Influence key stakeholders for embedded local resources. Establish team roles and responsibilities and time commitments for all team members.
• Manage project finances, contracts and vendors in accordance with budget and ensure adherence to government reporting requirements, if applicable.
• Develop detailed project schedules, including URS development, RFPs, vendor selection and management, equipment delivery and installation, raw material provisioning, master data changes, QC test method transfer, IQ/OQ/PQs, validation protocols/reports/VMP, automation modifications, LSOP/batch record revisions and approvals, Change Control, engineering runs, hand-over/training local operational team, and support for regulatory filing/submission.
• Execute project according to plan and maintain critical path. Monitor and communicate progress and ensure project outcomes meet project objectives. Proactively identify project risk areas or production impact and recommend mitigation or contingencies.
• Deliver final report at project completion including measurement of success, customer handover activities and recommendations for sustainability, project team after-action review, and lessons learned.
• Manage additional local projects as appropriate, and other duties as assigned.
• Manage and present project stage-gate reviews across project lifecycle, ensuring readiness criteria are met and decisions are clearly documented.
• Prepare, consolidate and deliver monthly project performance reporting to the PMO and governance forums, highlighting status, risks, issues, dependencies and recommended actions.

• Bachelor's degree OR Project Management certifications and 3+ years' experience in project management in a regulated industry.
• 3+ years project management experience in a regulated or complex industry.
• Proven experience managing cross-functional teams and stakeholder engagement.
• Experience managing vendors, contracts and project budgets.
• Knowledge of cGMP regulatory compliance standards and regulatory filings.
• Proficient in MS Project, Excel, Word, PowerPoint.

• Post graduate degree or related discipline and experience
• Project Management Professional (PMP) or similar certification.
• Experience in biotechnology, pharmaceutical, manufacturing, or highly regulated environments.
• Familiarity with Good Manufacturing Practice (GMP) principles and facility validation.
• Experience delivering multi-year or multi-million-dollar projects.
• Strong data analysis skills and ability to translate insight into action.
• Experience with change management and operational readiness activities.
• Ability to manage multiple projects and priorities simultaneously to meet deliverables within timelines and budgets.
• Ability to communicate effectively across all levels of the organization.
• Ability to work in a complex matrix and multi-cultural environment.
• Stay current on developments in the field and GSK Vaccines Standards.

This role is based in the United States and is on-site or hybrid depending on location and business needs. Specific working pattern will be discussed…