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 be responsible for maintaining accurate and compliant master data that enables safe, reliable, and uninterrupted supply to patients. This role supports material master data, production master data, production artwork management, and production line system data to ensure manufacturing and packaging operations can execute effectively. You will partner with local and global stakeholders across Operations, Quality, Supply Chain, Commercial, Technical Lifecycle Management (TLCM), and New Product Introduction (NPI) teams to support new material introductions, component changes, product launches, technology transfers, and lifecycle management initiatives. Success in this role requires strong attention to detail and deadlines, effective project coordination, ownership of data quality, and the ability to manage change in a regulated manufacturing environment. This role offers growth in technical skills, project experience, and impact on supply continuity as we unite science, technology, and talent to get ahead of disease together.
Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
Create and maintain material, production, and packaging master data within SAP and related manufacturing systems to support manufacturing, packaging, and distribution activities.
Coordinate new material introductions, product transfers, component changes, and lifecycle management activities with local and global stakeholders.
Support New Product Introductions (NPI), process optimization projects, regulatory labeling changes, and site performance improvement initiatives.
Create, review, and maintain packaging artwork and printed component data using artwork management systems, including project plans, impact assessments, artwork approvals, drawings, technical specifications, and supplier assignments for accuracy.
Partner with Technical Lifecycle Management (TLCM), Tech Transfer, Operations, Quality, Commercial, and Global Supply Chain teams to define and execute change-control strategies for material introductions and product changes.
Build and maintain strong relationships with Operations, QA, QC, Warehouse, Commercial teams, and global stakeholders to support successful project execution.
Support regulatory-driven changes and ensure alignment with regulatory filings, labeling updates, and market requirements.
Investigate and resolve master data, artwork, and system issues affecting manufacturing, packaging, or supply continuity.
Participate in change controls, deviations, CAPAs, audits, and continuous improvement activities as required.
Author, review, maintain, and improve SOPs, local procedures, and work instructions related to master data management, packaging artwork management, and manufacturing systems.
Perform all activities in accordance with GMP requirements, company policies, EHS standards, and applicable regulatory requirements.
Why You?
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
Bachelor’s degree in supply chain, business, engineering, life sciences, or equivalent experience may be considered.
2+ years of experience in master data, supply chain, or manufacturing support in a regulated environment.
Practical experience with ERP systems for material and production master data preferably SAP.
Preferred Qualification
If you have the following characteristics, it would be a plus:
Master's degree in business, supply chain, engineering, or life sciences
Experience with artwork management systems or similar packaging lifecycle platforms.
Experience with packaging line systems (Seavision preferred) or comparable manufacturing execution and packaging line applications.
Knowledge of GMP requirements, regulatory compliance, CAPAs, deviations, and change control processes.
Project management experience, including development of project plans, milestone tracking, risk management, and stakeholder coordination.
Experience working in a matrix environment with global and local stakeholders.
Proficiency with Microsoft Excel and other data analysis tools.
Demonstrated problem-solving skills with the ability to identify root causes and implement sustainable solutions.
Understanding of data governance, change control, and document management processes.
Strong attention to detail and commitment to maintaining accurate technical records and system data.
Ability to manage multiple priorities while meeting project timelines and business requirements.
Ability to work in a hybrid model, combining on-site presence with remote work as needed.
Clear written and verbal communication skills to work across teams.
What we value in you
You collaborate respectfully and communicate clearly across teams and functions. You take ownership of your work and demonstrate accountability for data accuracy and compliance. You are organized, adaptable, and capable of balancing operational priorities with project commitments. You continuously seek opportunities to improve processes, strengthen supply continuity, and support patients through reliable product delivery. You embrace different perspectives and contribute to an inclusive workplace where everyone can succeed.
Apply now
If this role matches your skills and ambitions, we would love to hear from you. Please submit your application and tell us how your experience will help strengthen master data and supply continuity.
#LI-GSK
#MariettaGSC
#GSKMarietta
Skills
Cold Chain, Customer-Focused, Customs Duties, Data Integrity, Digital Fluency, Financial Acumen, GxP Regulations, Lean Management, Logistics Management, New Product Introduction (NPI), Problem Solving, Product Knowledge, Risk Awareness, Strategic Alignment, Supply Chain Operations, Supply Chain Sustainability, Third Party Logistics Management, Transportation And Logistics, Warehouse Management
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 appropriate Recruitment Staff by emailing us at - usrecruitment.adjustments@gsk.com
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/