Qa System Validation Supervisor (Tamil Nadu)

Qa System Validation Supervisor (Tamil Nadu)

01 Aug
|
UPS
|
Tamil Nadu

01 Aug

UPS

Tamil Nadu

Before you apply to a job select your language preference from the options available at the top right of this page Explore your next opportunity at a Fortune Global 500 organization Envision cutting-edge possibilities experience our rewarding culture and work with talented teams that help you become better every day We know what it takes to lead UPS into tomorrow people with a unique combination of skill passion If you have the qualities and drive to lead yourself or teams there are roles ready to cultivate your skills and take you to the next level Job Summary The Healthcare Quality Assurance QA System Validation Supervisor provides guidance to UPS Supply Chain Solutions SCS Information Technology IT department to maintain validation of warehouse and or support systems utilized for healthcare applications This position assesses systems being evaluated for use in healthcare applications and provides training and subject matter expertise to achieve and maintain validated status He She identifies systems requiring validation elevates validation issues appropriately and provides validation expertise This position manages validation documents determines applicable regulations and reviews and approves testing of changes to validated systems Knowledgeable in 21 CFR Part 11 Annex 11 and GAMP 5 Updates validation procedures including change control training and audits to ensure the maintenance of system validation Writes and reviews technical validation documents e g validation plan URS FRS Risk Assessment Traceability Matrix IQ OQ PQ OPQ protocol report etc Assists in system validation project activities e g writing protocols reviewing approving test scripts drafting validation reports etc Review and approve Change Control requests and assesses the impact on system validation status Review and approve procedures forms and manuals Perform audit trail reviews and document results Perform system validation status evaluations and complete reports Assist with supplier qualification assessment data gathering Investigate review approve and perform corrective actions for deviations i e nonconformances and CAPAs and audit findings Maintains the document management system for healthcare facilities and distribution centers to ensure required documents and data are available for regulatory agency audits and inspections Supports internal and external audits Supports validation project status reports to communicate project goals contingency plans and issue resolutions to project teams and clients Supervise direct reports as appropriate Lead cross functional groups Flexible to work in different time zones Mandatory Skills Proficient with Microsoft Office applications Word Excel and PowerPoint Qualifications Bachelor s degree in a relevant field e g Information Technology Computer Science Data Science or related discipline Overall 7 years of experience with 2 years of experience in quality assurance manufacturing or compliance within a GMP-regulated industry Knowledgeable in 21 CFR Part 11 Annex 11 and GAMP 5 Must be an effective collaborator and communicator Must be well organized Must have proficiency with Microsoft Excel word and PowerPoint Knowledge of Process Analysis Continuous Improvement are required Tasks identified Provides guidance to UPS Supply Chain Solutions SCS Information Technology IT and Engineering departments to maintain validation of warehouse and or support systems utilized for healthcare applications Identify systems used in healthcare that require validation and assess and evaluate the applications for system validation requirements Consults with internal groups e g Operations Business Development IT etc and investigates and resolves healthcare issues to ensure compliance with rules and regulations Employee Type Permanent UPS is committed to providing a workplace free of discrimination harassment and retaliation

📌 Qa System Validation Supervisor (Tamil Nadu)
🏢 UPS
📍 Tamil Nadu

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