About this role
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 legiblyUse 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