Highland Park, IL Candidates need to be able to work in the City or State specified – Temporary, Full-Time
Title: Compliance Specialist
Location: Highland Park IL USA
Job Reference #:US33YESC_BH1421618
Work Type: Full Time
Employment Type: Temporary/Contract
Career Level: Experienced (Non-Manager)
DO YOU HAVE COMPLIANCE SPECIALIST EXPERIENCE IN THE PHARMACEUTICAL INDUSTRY AND LOOKING FOR A GREAT OPPORTUNITY TO START ASAP?
This Contract position is something you will not want to miss!
Quality Documentation Duties
Responsible for reviewing all data and documentation reported from the ANDA Report and investigating any identified discrepancies.
Facilitates data or documentation corrections with analysts to ensure the ANDA Reports and related records are complete and appropriate references are made.
Interacts closely with Management and all team members to identify and aid in the execution of investigations and implementation of corrective/preventive actions.
Interacts routinely with departments such as Production, QA, RA, R&D, Validation
Compliance Specialist Requirements
Knowledge of the global regulatory and quality requirements for the manufacture and testing of drugs, medical devices and veterinary products.
Knowledge of quality systems, manufacturing and testing processes in a pharmaceutical industry.
Thorough understanding of the CAPA methodology.
5-7 years lab experience in the pharmaceutical/ biotech industry
Compliance Specialist Additional Information
8:00am -5:00pm with 2-3 days working remote
Auditing , Manufacturing , Lab & Technology , Pharmaceutical
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