Maintain inventory of stability materials, reserve samples and reference standards, placing them into their assigned environmentally controlled locations as well as purging these materials from inventory per retention schedules.
Maintain environmentally controlled chambers, dispensing laboratories and own work space in a continuous orderly audit-ready state.
Performance and/or verification of physical inspections of reserve samples in support of product complaints, investigations or annual reviews.
Maintain accurate, legible, contemporaneous and thorough documentation of recordable stability, reserve sample and reference standard activities.
Function as a Controlled Drug Analyst
Minimum of High school graduate; Bachelor's degree or Associate degree desired.
2+ years of overall experience in Manufacturing, Quality or Engineering. Knowledge of GMP regulations and standards affecting pharmaceutical products.
Must be able to achieve goals in a compliance regulated and performance driven environment.
Some analytical or visual inspection experience with evidence of strong attention to detail.
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
Support the Stability Program to assure studies are place in chambers and that samples are dispensed accurately and in a timely manner. Support the Reference Standard Program to ensure standards are stored, inventoried and dispensed in an accurate and timely manner. Ship samples domestically and international following requirements for shipping dangerous goods and/or controlled substances. Accurately, legibly and contemporaneously document these activities following current Good Manufacturing Practice guidelines and applicable procedures. Perform and verify visual inspections of reserve samples as part of complaint investigations, annual product reviews or other exception events. Maintain a neat and orderly work environment in a continuously audit ready.
Abbvie · North Chicago, IL