GSK · 9 hours ago
Project Manager
Marietta, PA
Full-time
Hybrid
Mid, Senior Level
3+ years expGSK is a global biopharma company that manufactures and supplies medicines and vaccines to improve patient health. The Project Manager will lead projects aimed at enhancing operational efficiency and customer service, ensuring that projects are completed on time, within budget, and to the required quality standards.
BiotechnologyHealth CarePharmaceutical
Responsibilities
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 but not limited to activities such as; 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 appropriate mitigation or contingencies
Deliver final report at project completion including 1) measurement of success of the project and deliverables defined in the project charter addressing timelines, scope and specifications 2) customer hand-over activities and recommendations for sustainability, 3) Project team AAR, and 4) 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
Qualification
Required
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
Preferred
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 in order to achieve deliverables and adhere to timelines and budgets
Ability to achieve effective execution of complex projects and programs
Driven by delivering 'On time, on cost, and on specification' through a team
Ability to communicate both verbally and in writing with all levels of the organization. The ability to communicate ideas and concepts in a clear, compelling way
Personally agile in a political situation, will not compromise objectivity, independence or project governance
Ability to make oral group presentations and facilitate team discussions to include persuading others, providing information, explaining concepts, and delivering business cases
Creates culture of openness and objectivity, so issues and risks are well managed
Executive capability and leadership to manage people and field projects teams
Must be able to provide leadership to generate options, resolve problems, prioritize solutions, select optimal solutions and implement decisions
Able to interact in multidisciplinary environment including engineering, facility operations, validation, production and QC\QA. Ability to work across functional disciplines
Ability to work in a highly complex matrix and multi-cultural environment
Ability to effectively influence across functions at all organizational levels
Stay current on developments in the field and GSK Vaccines Standards
Company
GSK
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10001+ employees
H1B Sponsorship
GSK has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (45)
2024 (56)
2023 (54)
2022 (53)
2021 (54)
2020 (72)
Funding
Current Stage
Public CompanyTotal Funding
$25.51MKey Investors
CARB-X
2021-03-02Grant· $18M
2020-09-23Grant· $7.51M
1978-01-13IPO
Leadership Team
Julie Brown
CFO
Mike Elmore
SVP & Chief Information Security Officer, GSK
Recent News
2026-02-03
2026-01-16
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