GSK · 3 hours ago
Supply Chain Program Manager
Marietta, PA
Full-time
Hybrid
Senior Level
5+ years expGSK is a global biopharma company committed to manufacturing and supplying high-quality medicines and vaccines. The Supply Chain Program Manager will support the Site Logistics Director in managing projects that drive continuous improvement and ensure compliance with safety and quality standards in the supply chain.
BiotechnologyHealth CarePharmaceutical
Responsibilities
Develop yearly Safety Plan as fundamental for a safe work environment
Responsible for timely completion of deliverables
Identification of projects and initiatives that drive continues improvement in a constant changing environment
Managing and executing projects in collaboration with involved stakeholder
Frequent reporting to Site Logistics Director about progress, risk and opportunities
Support other local and global projects as directed
Development, management and adherence of Capital Expenditure Budget
Frequent reporting as defined
Perform evaluation to ensure site compliance with regulatory and internal standards for procedures management, change management and deviation investigation
Manage regulatory compliance with GMP, OSHA, FDA, EPA, DOT & EU
Controlled substances are tightly controlled and monitored
Act as business owner for improvements of business processes and SAP utilization for WMS, PP-PI, and SCM modules
Interact with global teams to share best practices and influence improvements
Accountable for transportation management in Marietta
This includes technical assessments of service providers (trucking companies, airports, harbors, etc.…), route approval, and the completion of tripartite business reviews and inspections
Act as the site Technical Expert for all questions and issues related to Cold Chain
Key contact regarding subjects for other sites and outside contacts, receive the information and distribute to appropriate members of the site
Become the site leader in the technology – attend conferences, develop technical expertise, conduct onsite training, etc
Act as the site consultant for each area of technical expertise when issues arise
Assist with deviation and investigation handling for areas of expertise, lead investigations when appropriate
Assist with project definition during design of projects that involve area of expertise including support of IQ/OQ/PQ
Be site review participant for GSOP development in their area of expertise to provide key review output from Marietta to assure the site needs are being addressed and improve our standing with GQA
Provide functional expertise to exchange best practices with site
Establish and maintain recurrent process to identify departmental risks
Together with risk owner identify appropriate mitigations
Facilitate regular risk meeting for in-depth reporting
Qualification
Required
Bachelor's degree in supply chain, engineering, business, or related field in Pharmaceutical Manufacturing or Quality Assurance
5+ years' experience with exposure to Warehouse/Supply Chain Processes, within a multinational manufacturing environment
Experience leading cross-functional teams and multiple stakeholders
Experience with project management tools and structured methodologies
Experienced communicating with all levels within an organization
Preferred
Full understanding of GMP's, DOT, OSHA, EPA and other applicable regulatory agency requirements with demonstrated success in application
Excellent organizational skills and attention to detail, ability to function in an atmosphere of constant change with detailed accuracy
Demonstrated interpersonal skills. The ability to function within team-based organization
Ability to establish and maintain working relationships locally and globally and the ability to analyze data and implement changes
Ability to lead the process to generate the exchange of ideas to resolve problems, prioritize solutions, select optimal solutions and implement decisions
The ability to communicate effectively, both verbally and in writing, to all levels within the organization as well as the skills to communicate site operations to outside agencies
Advanced computer skills in Microsoft Office applications and the ability to quickly and easily learn new applications
Able to interact with peers, subordinate and senior personnel in multidisciplinary environment including engineering, facility operations, validation, production and QC. Ability to work in a high complex matrix environment
Able to prioritize and decide appropriate course of actions and to effectively implement decisions
Capable of working without direct supervision
Familiarity with Good Manufacturing Practices and NIH guidelines
Sense of urgency, flexibility and accountability
Ability to follow written procedures and document results in a neat and precise manner
Stay current on developments in the field and GSK Standards
Work within a multi-skilled team
Demonstrate a serious commitment to accuracy and quality while meeting goals or deadlines
Maintain a high level of integrity while balancing multiple priorities and responsibilities
Company
GSK
We are uniting science, technology and talent to get ahead of disease together. Our community guidelines: https://gsk.to/socialmedia
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
2026-01-16
2026-01-13
South China Morning Post
2026-01-08
Company data provided by crunchbase