Provides consistent and thorough exception documents and timely resolution of investigations based on CAPA requirements
Coordinates the exception document process and creates exception documents
Promotes culture of continuous improvement by identifying problems, conducting root cause analysis and confirming appropriate implementation of corrections, corrective and preventive actions
Ensures all investigations are written according to corporate and site requirements
Participates in implementation and maintenance of the Quality System to meet all applicable regulatory requirements
Effectively collaborates/partners with other Quality areas and departments within the plant
Bachelor's degree required.
Preferably in one of the following areas: Biology, Chemistry or Engineering.
4+ years of experience in the pharmaceutical industry in Manufacturing, Quality or Engineering.
Ability to problem solve and utilize analytical skills.
Knowledge of Quality/Compliance management, Regulations and Standards.
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
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:
Dental insuranceVision insurance401(k)Paid time offPerformance bonus
Additional Information
Performs root cause investigations for exceptions/nonconformities/deviations to required procedures and/or specifications for drug product manufacturing and packaging.