Quality Control Analyst

  • AbbVie, Inc
  • Edmonton, Kentucky
  • Full Time

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

We are recruiting Quality Control Analyst (12 months) to join our diverse team in Cork. ( Shift Position)

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  • Execute analysis of raw materials, in-process material, and finished product in compliance with schedule.
  • Complete analysis in accordance with SOP and standard methods.
  • Execute analysis of water, cleaning samples etc as required.
  • Execute calibrations and PM of equipment as required to ensure equipment is appropriate for use for analysis.
  • Co-ordinate maintenance schedules with external suppliers to ensure compliance with schedule and in house procedures.
  • Preparation of all solutions, reagents etc. associated with analysis.
  • Execute stock control on laboratory consumables including reagents, solvents to ensure there is adequate supply to execute tasks. Complete purchase orders as required and manage materials on receipt.
  • Participate in the preparation of QC documents including SOPs, specifications, methods.
  • Participate in training and development activities to ensure that new technologies are applied and that skill level is developed.
  • Execute validation studies and transfer studies to ensure equipment, methods and personnel are appropriately qualified.
  • Participation in QC and site projects by representing QC so as to provide an appropriate service to other departments
  • Ensure QC activities are executed in line in in-house procedures and in compliance with requirements of cGMP.
  • Ensure QC activities are executed in line with safety requirements and good laboratory practice.
  • Keep work area clean and tidy.
  • Keep up to date on regulatory development and standards by accessing in house library, accessing current Pharmacopoeias etc.
  • Participation in investigations into failures, out of trends and out of specifications as required.

Qualifications

  • Degree in an analytical science/biochemistry/toxicology is preferred
  • Previous experience in a laboratory environment and direct experience of HPLC analysis would be an advantage
  • Analytical approach to tasks. Good organisation skills. Technical skills in analysis are important. Microsoft office suite ( excel / word)

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.

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Salary:

Job ID: 486285637
Originally Posted on: 7/22/2025

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