Jobs / United States / Abbott Laboratories
Engineer, Manufacturing
Abbott Laboratories · 🇺🇸 United States > Madison : 650 Forward Dr
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 73 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 28 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 Abbott Laboratories paid sponsored hires in similar roles2 certified filings for “Senior Manufacturing Process Engineer” (Industrial Engineers) in TX: $91k–$130k, median $110k. Most were filed at wage level II (100%) — 2 lottery entries, ≈31% 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 — Abbott Laboratories
The US Department of Labor certified 73 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 28 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 Abbott Laboratories →
About the role
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries. JOB DESCRIPTION: Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: • Career development with an international company where you can grow the career you dream of. • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. • An excellent retirement savings plan with a high employer contribution. • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity This position works out of our Madison, WI location in the Cancer Diagnostics Division. The Manufacturing Engineer will support cross-functional engineering activities within Operations under the guidance of senior engineers and functional leaders. This role will contribute to the design, development, transfer, and improvement of manufacturing processes and capabilities for reagent and collection kits, packaging components, and automation-related projects. The role will also support Supply Chain and internal stakeholders by helping coordinate technical activities with external Contract Manufacturing Organizations (CMOs), assisting with troubleshooting, maintaining documentation, and supporting continuous improvement efforts to help ensure product quality and compliance with internal specifications. Essential Duties Include, but are not limited to, the following: • Support technical projects and cross-functional initiatives with guidance from senior engineers, project managers, and functional leadership. • Provide engineering support on assigned projects by gathering data, documenting findings, and helping coordinate technical activities with project teams. • Assist with specification, procurement, implementation, and modification of engineering controls and manufacturing solutions to support process improvements, volume growth, and new product introduction. • Help identify process efficiency, cost savings, and quality improvement opportunities and support execution of related project tasks. • Support the design, development, testing, and documentation of reagent and collection kit components, packaging solutions, and related manufacturing processes. • Assist with collecting, organizing, and summarizing project data to support cross-functional decision-making and stakeholder understanding of cost, schedule, quality, and risk trade-offs. • Create, revise, and maintain documentation such as standard operating procedures, user requirements, design specifications, component specifications, commissioning protocols, test records, and engineering reports with appropriate review and approval. • Participate in investigations and troubleshooting activities related to manufacturing processes, internal reviews, CAPA, audits, or complaints. • Demonstrate strong documentation practices, attention to detail, and willingness to learn within a GMP-regulated environment. • Uphold company