Qc Coordinator 2

**Summary**Assist with the day-to-day operations associated with Control of Nonconforming Materials. Assist management to ensure that products, procedures, and processes comply with applicable regulations and standards.**Essential Duties and Responsibilities**- Perform physically quarantine nonconforming material.- Perform electronic inventory transactions to prevent unintended use.- Execute activities per approved material disposition- Facilitate NCMR processing in the electronic system- Monitor NCMR trending, follow-up NCMR status, and reporting- Maintain inventory under Quality Control through transactions and cycle counts.- Assist with the identification and organization of quality records associated with Nonconforming Material with cross department personnel- Support investigations into potential quality/compliance concerns.- Support routine walk-through activities- Perform other tasks as assigned to enable organizational and quality objectives to be met.**Required Qualifications**- Minimum 3 years working in the medical device, pharmaceutical, or other regulated industry in the Quality Assurance department.- Understanding of Quality Management Systems (QMS) as applied to medical devices- Proficiency with Microsoft Office, ERP System- Ability to communicate effectively and clearly.- Ability to work hands-on in a fast-paced environment- Must be able to flex schedule to work in different shifts to support commercial run.