Jobs / United States / Glaxosmithkline LLC
Equipment Engineer (MDPI)
Glaxosmithkline LLC · 🇺🇸 USA - North Carolina - Zebulon
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 “Software Engineer - AI/ML Services” (Software Developers) in CA: $184k–$184k, median $184k. 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 serve as the MDPI Equipment Engineer, providing mechanical and automation expertise to support safe, reliable manufacturing. You will work closely with Production, Engineering, Maintenance, Quality, Facilities, Automation and EHS to deliver continuous capital projects and day-to-day production support. We value practical problem solvers who collaborate clearly, act with integrity, and drive improvements that make a real difference to patients. This role offers chances to grow technically, lead projects, and contribute to a mission that unites 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: • Provide hands-on mechanical, instrumentation and controls troubleshooting on production equipment and peripheral systems. • Lead design, installation, commissioning, qualification and continuous improvement activities for equipment and automation. • Partner with cross-functional teams and external contractors to deliver projects on time, within scope and compliant with regulations. • Support investigations, root cause analysis and corrective actions for equipment and process issues. • Mentor technicians and junior engineers, share best practice, and support capability development. • Contribute to equipment lifecycle documentation including FAT, SAT, commissioning records and validation deliverables. Why You? Work arrangement This position is on-site in the United States. Hybrid or remote work is not available for this role. Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals: • Bachelor’s degree and 5+ years' experience in mechanical, electrical, automation, chemical engineering or related technical discipline; or equivalent practical experience supporting production equipment, automation or controls in a Pharma or Medical Devices regulated manufacturing environment -or- • AAS degree in Technical field (i.e. Industrial Automation, Electronics, Robotics) and 10+ years' experience supporting production equipment, automation or controls in a Pharma or Medical Devices regulated manufacturing environment. • Experience with mechanical and automation troubleshooting on production equipment. • Experience delivering equipment projects, installations or upgrades from design to handover. Preferred Qualification If you have the following characteristics, it would be a plus: • Experience in pharmaceutical, biologics or other highly regulated industries. • Knowledge of automation systems such as PLC, HMI, SCADA and MES and familiarity with related wiring, networking and instrumentation. • Understanding of qualification and validation activities including FAT, SAT, commissioni