Project Manager at GSK

Marietta, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

20 Feb, 26

Salary

0.0

Posted On

22 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Management, cGMP Compliance, Stakeholder Engagement, Vendor Management, Budget Management, Data Analysis, Change Management, Operational Readiness, Cross-Functional Team Leadership, Regulatory Compliance, Communication, Problem Solving, Agile Methodologies, Documentation, Risk Management, Scheduling

Industry

Pharmaceutical Manufacturing

Description

Site Name: USA - Pennsylvania - Marietta Posted Date: Nov 21 2025 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 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. 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. The Project Manager will be responsible for the complete lifecycle management of projects that will consist of: 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. Responsibilities: Create clear project charters, schedules and success criteria. Coordinate procurement, equipment installations, testing and operational readiness activities when required. Ensure projects meet quality standards and applicable regulatory or safety requirements. Use data and customer insight to inform project decisions and improvements. Support change adoption through stakeholder engagement and training plans. Maintain accurate documentation and final project reports. Why You? Basic Qualification: We are seeking professionals with the following required skills and qualifications to help us achieve our goals: 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 Qualification: If you have the following characteristics, it would be a plus: 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. Working arrangement: 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 during the hiring process. What we value We create a welcoming work environment where people can do their best work. We commit to inclusion and to helping colleagues grow. We want people who work with integrity, show respect, and who learn and adapt. If you are ready to take ownership of meaningful projects and help us improve how we serve patients and customers, we would like to hear from you. Ready to take the next step? Apply now to join our team and help deliver projects that make a real difference. #LI-GSK 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/

Responsibilities

The Project Manager will lead projects to improve operations and customer service, ensuring they are completed on time, within budget, and to quality standards. Responsibilities include managing project scope, resources, finances, schedules, and stakeholder communication.