About this role

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, FacebookInstagramX and YouTube.

Job Description

  • Conduct chemical and physical laboratory tests and analyze excipients, cleaning samples, raw materials, intermediates, and final products including protocol testing in a timely manner to ensure compliance with standards and production targets.
  • Recognize and report to immediate supervisor any issues or deviations from accepted standards.
  • Provide status updates on own activities and productivity challenges according to defined procedures
  • Maintain data integrity and ensure compliance with FDA, GLP, QSR and cGMP regulations, as well as with company SOPs and specifications.
  • Complete and conform to all training requirements for job role, including company-required and job role-specific training.
  • Observe all safety and compliance procedures and actively highlighting any safety concerns to help drive the reduction of accidents or near misses.
  • Conforming to the safety culture on site on Zero, Believe it, Achieve it.
  • Participate in the 6S activities within the QC Laboratory.
  • Positively contribute to departmental goals and programs such as Right First Time

Qualifications

  • A third level qualification in Chemistry or related Science, preferably a Bachelor’s Degree
  • Graduate with a third level qualification in Chemistry or related Science.
  • Demonstrate knowledge of cGMP requirements and practices including knowledge of the USP and FDA
  • Guidance Documents relating to the pharmaceutical Quality Control Laboratory.
  • Demonstrate knowledge of common analytical instrumentation e.g. HPLC, Dissolution, GC, FTIR, Electro Chemistry (DME), UV/Vis and other USP instrumental and Wet chemistry technologies used in pharmaceutical Quality Control Laboratory.

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

Frequently Asked Questions

Is the salary disclosed for the Analyst, Quality Control position at abbvie?
The salary for this Analyst, Quality Control role at abbvie is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Analyst, Quality Control position at abbvie located?
This Analyst, Quality Control role at abbvie is based in County Dublin, Dublin, Dublin, County Dublin, Ireland, ie. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Analyst, Quality Control role at abbvie full-time or part-time?
This is listed as a Full time position. It is posted as a Analyst, Quality Control role at abbvie.
How do I apply for the Analyst, Quality Control position at abbvie?
Click the "Apply Now" button on this page. You will be redirected to abbvie's official application portal hosted on smartrecruiters where you can submit your application directly.
When was the Analyst, Quality Control job at abbvie posted?
This Analyst, Quality Control position at abbvie was posted on Aug 28, 2026. Apply as soon as possible — early applications are often reviewed first.
Analyst, Quality Control
abbvie
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