Jobs / Ireland / Abbvie US LLC

Abbvie US LLC

Documentation and Compliance Specialist

Westport, MO, IE Posted today

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Skills this job asks for

ComplianceSAPSupply chain

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Sponsorship verdict

No sponsorship evidence yet

No government record and no wording either way. Not a refusal: ask the recruiter.

  • No government sponsor record hereNo government sponsor record covers this employer in this country.
  • The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
  • Can’t check pay against the visa rulesNo salary stated. Ireland Critical Skills Employment Permit needs at least €40,904 a year (General Employment Permit: €36,605).
  • Confirmed live todayWhen a source last listed this job as open.
Details and sources
Can’t check pay against the visa rules
No salary stated. Ireland Critical Skills Employment Permit needs at least €40,904 a year (General Employment Permit: €36,605). Source: https://enterprise.gov.ie/en/what-we-do/workplace-and-skills/employment-permits/permit-types/critical-skills-employment-permit/, rules effective 2026-03-01.

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Before you apply

Sponsorship unknown

No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.

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About the role

• Issue production batch records, worksheets, packaging records, and related controlled documents using approved systems and current effective versions. • Assign and verify batch numbers, process order numbers, and document revisions prior to issuance.  • Ensure only current, approved documentation is issued for manufacturing use. • Print, prepare, stamp, and control manufacturing documentation according to site procedures.  • Maintain document accountability, issuance logs, and controlled records. • Support Manufacturing, Planning, Quality Assurance, and Process Sciences by preparing records for scheduled production activities. • Process requests for additional pages, replacement documentation, and document revisions while maintaining traceability. • Verify issued documentation is complete, legible, accurate, and attributable to the correct batch.  • Maintain compliance with GMP, GDP, Data Integrity, and document control requirements. • Support investigations, audits, inspections, and document retrieval requests as required. (The procedures establish controlled-document accountability and retention activities.)  Typical Systems Used • SAP • Electronic Document Management Systems (eDMS/Vault) • POMSnet / MES (where applicable) • Batch record tracking and issuance tools  • Knowledge of GMP documentation practices. • Strong attention to detail and accuracy. • Experience with document control and records management. • Ability to work with Manufacturing, QA, Planning, and Supply Chain teams. • Proficiency with SAP and document management systems. • Strong organizational and compliance mindset. 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

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