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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 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
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
- Perform Chemistry analysis of In process / Final product as per schedule and in accordance with regulatory requirements.
- Perform analysis on Stability samples from a wide range of products.
- Documenting all testing activities, results and raw data on time, accurately and legibly
- Use of laboratory IT systems including LIMS and Empower.
- Reviews and interprets test results.
- Adhering to all company standards in the areas of safety, housekeeping and quality, notifying management of any discrepancies.
- Ensure good housekeeping and good laboratory practices.
- Work with team, Supervisors, Quality Manager and Laboratory Manager to ensure compliance to Quality Management System.
- Good knowledge and understanding of Data Integrity from Laboratory perspective.
- 3rd Level Qualification in a Science Discipline, preferably Chemistry related.
- 1-2 Years’ experience working as an Analyst in a GMP/GLP environment.
- 1-2 Years’ experience of working with a range of Analytical Equipment specifically HPLC and GC and well as other laboratory techniques.
- Experience and good knowledge of Empower.
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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- Posted
- Feb 11, 2026
- Type
- Full-time
- Level
- Entry
- Location
- Westport
- Company
- AbbVie
Industries
Pharmaceutical Manufacturing
Biotechnology Research
Categories
Research
Analyst
Information Technology
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Pharmaceutical Manufacturing
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