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Senior NPI Compliance Specialist

AbbVie Inc. - Sligo, SO, Ireland

Posted Jun 10, 2026

Benefits

Parental leave
12 weeks From the posting source
Non-birth-parent leave
12 weeks From the posting source
Family-building benefits
  • Fertility benefits: Not verified
  • Adoption assistance: Not verified
  • Surrogacy assistance: Not verified
Mental health support
Not verified
Relocation assistance
Not verified
Childcare support
Not verified
Learning budget
Not verified
Verification
Source-linked checked May 7, 2026
Salary
Not verified
401(k) match
Reported from DOL Form 5500 industry filing (not employer-specific)

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Market context

U.S. role benchmark (BLS OEWS)
$106,409 U.S. median for this role
Projected growth (BLS Employment Projections)
+7.7% - Faster than average

Matched to SOC 13-2011 - Finance aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function
Finance From the posting source
Seniority
Senior From the posting source

Schedule

Shift type
Not verified
Weekend work
Not verified

Company

Equity
Offered Verified - SEC 10-K source

Application

Cover letter
Not verified
Assessment
Not verified
Deadline
Not stated

Where they hire

State eligibility is not yet verified.

About this role

Senior NPI Compliance Specialist Sligo, SO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: AbbVie is seeking a Senior NPI Compliance Specialist to support the compliant transfer of new products to AbbVie Sligo for a fixed-term contract of 12 months. The role ensures products are manufactured in line with regulatory requirements, AbbVie procedures, and quality standards, working closely with cross-functional teams from development through commercialisation. Responsibilities Maintain the effectiveness of the new product integration within the NPI quality system. Ensure new products meet applicable regulatory requirements and AbbVie policies. Support product transfers from development through commercialisation, including quality risk assessment and mitigation. Manage vendor evaluation and approval, including technical agreements. Review and approve NPI-related analytical test method transfers and/or validation. Collaborate with CMC QA, R&D, S&T, and other functions on quality issues and compliance inputs. Coordinate review of product-related material specifications, including API, drug product, raw material, excipient, and intermediate specifications. Support exception documentation and CAPA actions to prevent recurrence. Prepare product transfer documentation for stage gate reviews. Act as a subject matter expert during

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