AbbVie CAPA Investigator (m/f) in Palatinate, Germany

Your Responsibilities: * Investigation of exception events (root cause analysis) * Investigation of Product Complaints for the AbbVie Ludwigshafen site * Compilation, review and approval of Exception Reports (NCR, pNCR, LIR) * Scheduling and tracking/trending of Corrective Actions and Preventive Actions via the Soltraqs data base * Support of the head of Quality Assurance Operations in the implementation of intersite QA measures of GMP exception events and their prevention * Coordination of the GMP system and CAPA activities at AbbVie Ludwigshafen (e.g. sam-ple shipment, responsibility for equipment etc.) * Contact for the departments regarding GxP related questions connected to exception events/CAPAs * Data administration in the Soltraqs exception management system * Support of the Quality Control regarding CAPA, process optimization, communication with contractors * Verification of internal/external environmental and safety guidelines * Verification of the GMP status of the laboratory * Contribution to the testing of medicinal products, APIs, excipients and packaging

Your Profile: * Degree in pharmacy (state examination/German Approbation) * Doctoral degree in pharmacy/pharmaceutical science * Knowledge of regulatory and legal requirements for medicinal products (e.g. AMG, AMWHV) * Knowledge in pharmaceutical analytics * Experience in the evaluation of analytical results and methods * Fluent english skills

We are looking forward to your online application and ask that you state your salary and your earliest start date or notice period in your personal statement. AbbVie is characterized by diversity and internationality. We therefore welcome diversity among our applicants, in particular also chronically ill and severely disabled people.

Job Classification: Experienced
Primary Location: Germany-Rhinland-Palatinate-Ludwigshafen
Organization: Operations
Schedule: Full-time
Shift: Not required
Travel: No
Req ID: 1607209