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Senior NPI Compliance Specialist

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Sligo, SO

  1. Operations
  2. Hybrid
  1. Full-time
R00142983
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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 internal audits and external regulatory inspections.

Qualifications

  • Third-level qualification in science, quality, or a related discipline.
  • Minimum of 5 years’ experience in a quality role supporting new product introductions.
  • Preferred: QP eligible, or actively working toward QP eligibility, with an interest in pursuing Qualified Person status in the future.
  • Strong knowledge of regulatory requirements.
  • Excellent attention to detail, problem-solving, and decision-making skills.
  • Strong communication, interpersonal, and collaboration skills.

Additional Information

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

Recruitment Fraud Alert

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If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately.


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