Jobs / United States / Glaxosmithkline LLC
Master Data Specialist
Glaxosmithkline LLC · 🇺🇸 USA - Pennsylvania - Marietta
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- Employer is on a government sponsor recordThe US Department of Labor certified 39 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 15 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- What Glaxosmithkline LLC paid sponsored hires in similar roles1 certified filing for “Sr Manager - Oncology Commercial Analytics, Multiple Myeloma” (Data Scientists) in PA: $135k–$135k, median $135k. Most were filed at wage level III (100%) — 3 lottery entries, ≈46% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
- Confirmed live todayWhen a source last listed this job as open.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
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Sponsor Radar — Glaxosmithkline LLC
The US Department of Labor certified 39 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 15 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Glaxosmithkline LLC →
About the role
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.