Supply Chain Program 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; its 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

The Supply Chain Program Manager is a cross functional role within the Supply Chain department. The position supports to meet customer expectations for Safety Quality Supply and Cost in alignment with all applicable external and internal standard and policies.

The position supports the Site Logistics Director in identifying and leading projects that drive continues improvement as well as managing annual budget.

Responsibilities:
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• EHS Safety Plan

  • Develop yearly Safety Plan as fundamental for a safe work environment.

  • Responsible for timely completion of deliverables

• Supply Chain Project Management

  • 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.

• Accountable for Capital Expenditure Budget

  • development management and adherence

  • 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.

• Risk Management

  • establish and maintain recurrent process to identify departmental risks.

  • together with risk owner identify appropriate mitigations.

  • facilitate regular risk meeting for in-depth reporting.

Why You
This role is hybrid with regular time on-site in the United States and flexible remote work. You will join a team that values collaboration curiosity and continuous learning. You will be supported to grow your skills through coaching and practical stretch assignments. We welcome people who bring different perspectives and lived experience. You will be contributing to work that matters and seeing tangible results.

Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals

• Bachelors 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 Qualification
If you have the following characteristics it would be a plus

• Full understanding of GMPs 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.

#LI-GSK

How to apply
If this role matches your experience and ambitions we encourage you to apply. We look forward to learning how you can help us advance our supply chain capabilities and make a meaningful impact.

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 were 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.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at where you can also request a call.

Please note should your inquiry not relate to adjustments we will not be able to support you through these channels. However we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive

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 GSKs 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 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 GSKs compliance to all federal and state US Transparency requirements. For more information please visit the Centers for Medicare and Medicaid Services (CMS) website at Experience:

Manager