Jobs / United States / Abbott Laboratories

QC Applications & Data Specialist

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 roles5 certified filings for “SENIOR SPECIALIST QUALITY ASSURANCE” (Industrial Engineers) in IL: $105k–$142k, median $112k. Most were filed at wage level III (40%) — 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 — Abbott Laboratories

73 H-1B filings certified since Oct 2025

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: Position Overview: The QC Applications & Data Specialist will lead and/or participate in a variety of Quality Control functions relating to the automation and applications in use, including but not limited to, the Electronic Form Database (EFD), Data Trending, QC Analysis workbooks, Liquid Handling Automation Method Scripts, and quality documentation generation.  The position is responsible for implementation, tracking, trending, and reporting on these processes.    Essential Duties: Include but are not limited to the following: • Support of EFD processes, form development, and expansion for Quality Control. Subject Matter Expert in new, or updates to, test method EFD forms and their implementation. • Leads or supports project activities associated with Quality Control Applications and Automation, which may include leading the creation and/or implementation of liquid handling method scripts. • Utilize basic knowledge of statistics and interpretation of analyses to draw conclusions from data summaries. • Support or lead the development, validation, implementation, and improvements of test method specific QC Analysis Workbooks for data evaluation and disposition using SAS JMP Statistical Software, or similar software. • Participates in Deviation report generation and CAPA efforts pertaining to QC Applications used.  • Lead and/or mentor individuals to complete essential tasks relating to the QC applications and automation. • Draft and execute protocols for quality system software or analysis workbook Validation efforts in accordance with internal procedures, cGMPs, FDA, and ICH guidelines. • Write, update, and review of quality documents, including but not limited to, Standard Operating Procedures and Test Methods that are compliant with cGMP/GLP guidelines.  • Provide support in cross functional teams, as required. • Support and comply with the company's safety and environmental procedures. • Support the Operations department in other non-laboratory functions, as determined by Operations management. • Perform other related duties as assigned by management. • Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. • Support and comply with the company’s Quality Management System policies and procedures. • Ability to develop and follow procedures or experimental plans. • Ability to interface and work effectively within team and department, as well as all levels of the organization, vendors, customers, etc. • Ability to effectively work on many complex and varied projects at one time, with frequent changing priorities. • Ability to act with an inclusion mindset and model these behaviors for the organization. • Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 100% of a typical working day. • Ability to work on a computer and phone simultaneously. • Ability to use a telephone through a headset. • Ability to lift up to 40 pounds. • Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height. • Ability to comply with any applicable personal protective equipment requirements. • Ability and means to travel 10% between local Madison, WI locations. • Ability to travel 5 % of working time away from work location, may include overnight/weekend travel. Minimum Qualifications: • Bachelor’s d

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Source: Employer career site (Workday) First seen: 2026-10-08 Last confirmed: 2026-10-08 How our data works → Report this job

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