AbbVie
Onsite
Full Time Mid-Level Posted 3 days ago
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powertofly approved What AbbVie Has to Offer:

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.

Job Details


Company Description

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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.


Job Description

AbbVie Biologics Ballytivnan in Sligo invites applications for the Incoming Quality Assurance Supervisor role in our Quality Assurance department. Reporting to the Quality Operations Manager, this position is pivotal in ensuring materials released for both marketed and investigational drug products meet stringent AbbVie standards. You will oversee the IQA process, lead investigations, support continuous improvement, and collaborate across teams to drive quality, safety, and compliance.

Responsibilities

  • Oversee and ensure timely, compliant release of all incoming materials for manufacturing
  • Manage and provide guidance on sampling requirements, especially for aseptic processes
  • Lead IQA-related investigations and coordinate with contract laboratories
  • Review, audit, and author material release records, specifications, and SOPs
  • Act as site SME for SAP inspection plans and material management; support internal and regulatory audits
  • Drive process simplification and improvements
  • Guide cross-functional and cost improvement initiatives, championing quality in new product introductions
  • Supervise up to 5 team members, fostering collaboration and maintaining a high standard of work
  • Promote and uphold EHS policies, supporting a culture of safety excellence

Qualifications

  • Bachelor’s degree or above in science, quality, or engineering
  • At least 3 years of experience in GMP-regulated quality or operations roles in pharma or biopharma industries
  • Desired:  Previous people supervision
  • Strong regulatory knowledge, attention to detail, and effective problem-solving skills
  • Proven cross-functional collaboration, leadership ability, and solid communication 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

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Incoming Quality Assurance Supervisor
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