QA-RA Specialist at UPSJob SummaryThis position monitors the overall Quality System status of the distribution center, acting in compliance with drug, medical device, and local regulations. It ensures quality processes are maintained through the implementation of procedures, training, and regular inspections.ResponsibilitiesEnsures all staff is trained in their respective job functions, including GMP.Writes and revises Standard Operating Procedures as required.Conducts regular inspections of the facility and recordkeeping, including summarization and reporting of findings; coordinates or assists with corrective actions and preventative measures.Communicates with clients and provides information during external audits.Liaises with Health Canada officials during regulatory audits.Provides feedback and assistance to Customer/Client QA related questions and concerns.Monitors the processes and systems within the Department to ensure regulatory compliance and effective operation.Investigates discrepancies and problems, and advises the appropriate individuals of the findings.Assists in development of proactive strategies as a pre‐emptive measure against potential future problems with systems or processes.Completes NCR reports and change control requests and provides necessary follow‐up.Performs maintenance, support, and continuous improvements of Quality Systems.QPIC designation duties.QualificationsPharmaceutical, healthcare, or food industry experience - PreferredQuality Assurance Experience - PreferredBachelor's Degree in Pharmacy or Chemistry and Pharmaceutical Technology or similar for technical direction (GDP Responsible person/back up)Contract TypePermanentTime TypeFull timeLocationSomagliaEmployee TypePermanentUPS is committed to providing a workplace free of discrimination, harassment, and retaliation.Seniority LevelEntry levelEmployment TypeContractJob FunctionQuality AssuranceIndustries: Truck Transportation
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