Quality Specialist

A company is looking for a Specialist Manufacturing. Key Responsibilities Address and close quality records (Deviations, CAPAs, Supplier Event Notifications, and Change Control) ensuring compliance with regulatory requirements Monitor and investigate deviations, implementing corrective and preventive actions while partnering cross-functionally Build and present quality records summaries for Senior Management review and provide timely updates on processes and statuses Required Qualifications 3-5 years of hands-on experience managing deviations, change controls, and CAPAs Experience with quality records in biotech or medical device industries Basic project management skills Bachelor's degree preferred; associate degree holders with significant experience (10+ years) may be considered Strong grasp of root cause analysis and investigation review

Jun 19, 2025 - 17:50

A company is looking for a Specialist Manufacturing. Key Responsibilities Address and close quality records (Deviations, CAPAs, Supplier Event Notifications, and Change Control) ensuring compliance with regulatory requirements Monitor and investigate deviations, implementing corrective and preventive actions while partnering cross-functionally Build and present quality records summaries for Senior Management review and provide timely updates on processes and statuses Required Qualifications 3-5 years of hands-on experience managing deviations, change controls, and CAPAs Experience with quality records in biotech or medical device industries Basic project management skills Bachelor's degree preferred; associate degree holders with significant experience (10+ years) may be considered Strong grasp of root cause analysis and investigation review