Jobs / United States / Abbvie INC
Senior Analyst, Quality Control
Abbvie INC · 🇺🇸 Sligo, IE
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 177 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 94 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 Abbvie INC paid sponsored hires in similar roles2 certified filings for “Senior Associate/Analyst, Regulatory Affairs Info Mgmt” (Regulatory Affairs Specialists) in IL: $98k–$105k, median $102k. 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 — Abbvie INC
The US Department of Labor certified 177 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 94 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 Abbvie INC →
About the role
What you do, is what we need. Making a difference begins here. And takes all of us. Welcome to AbbVie! We are a global, research-based biopharmaceutical company that combines the focus and passion of leading-edge biotech with the expertise and capability of an established pharmaceutical leader. Redefining what is possible is our business and our passion. Our goal is to help patients live healthier lives and we are proud to be a Great Place to Work. We are recruiting a Senior QC Analyst to join our QC team on site in Ballytivnan, Sligo on a perm contract. This is a day shift role. Some of your responsibilities will include: • Ensuring Analytical Laboratory Documentation and Computerized Systems compliance with Data Integrity policies and regulatory requirements. • Understanding Regulations and business processes required to maintain Laboratory Data Integrity. • Ensuring timely completion of all laboratory analysis assigned to shift. • Ensuring that analysts working in the assigned cell or team are performing to the best of their ability, coaching and providing guidance where issues occur such as poor set-up or test execution performance. • Improving the overall efficiency and velocity within the assigned team. • Identifying and implementing improvements in analytical practice using ‘Zero, Believe it, Achieve it’ • Ensuring that the agreed test schedule is adhered to and identifying recovery paths to bring test schedules back into alignment with plant requirements. • Identifying weaknesses in laboratory performance and working with the laboratory management to rectify. • Supporting & initiating analytical OOS issues as they arise in a timely manner both through practical work and through the quality system. • Ensuring 5S excellence is maintained across the Laboratory. • Executing and / or supporting projects through the Lab Management team. • Maintaining up-to-date, complete and precise records of all tests performed. • Developing expertise and understanding of current and future analytical techniques. • Developing and updating of in-house laboratory procedures as appropriate. • Carrying out verification of testing records & generation of Final CoA as necessary. • Positively contribute to departmental programs such as e-ACHIEVEs, and iCANs • Lead the transfer and validation of NPI analytical test methods to the QC Laboratory. • Lead validation of equipment for the QC Laboratory. • Adhere to and support all EHS & E standards, procedures and policies. • Development of training material and the training of QC analysts. • Lead and support any lab-related investigations. What you will need: • 3rd level qualification in the relevant science discipline • 4-5 years’ experience in a similar role within the pharmaceutical industry • Proven track record in an analytical role AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html