QC Inspector

QC Inspector

12 Nov 2026
Florida, Pontevedra, 32081 Pontevedra USA

QC Inspector

POSITION SUMMARYWe're seeking a detail-oriented Quality Control (QC) Inspector to join our dedicated team, working within our additive manufacturing operation. The successful candidate will be integral in ensuring that all operations within these areas adhere to our rigorous standards, as defined by current Good Manufacturing Practices (cGMP).This role demands precision, a strong commitment to quality, and a keen understanding of the vital processes and procedures associated with cleanroom environments. A passion for patient safety and value are critical for success.The candidate must possess the ability to work cross-functionally to support rapid growth and continuous improvement. This position will interact with many functions and levels of the business.PRIMARY DUTIES & RESPONSIBILITIES:Inspection of work-in-progress, finished parts and assemblies, kits and completion of associated paperwork for final release of productAssemble non-sterile product into kits for final release into the fieldVisually and dimensionally inspect products to ensure that they meet quality specifications.Participate in the establishment of future inspection procedures.Review device history records to ensure that they are complete and accurate.Identify and author any product nonconformances, working closely with Operations to resolve.Participate in the setup, calibration, and maintenance of inspection equipment.Engage in various manufacturing operations, ensuring all activities align with our established standards and cGMP protocols.Adhere to safety protocols and contribute to the continuous enhancement of product quality through meticulous attention to detail.Perform post-processing monitoring to ensure conformance to quality standards.Work in tandem with the Manufacturing management team and manufacturing associates ensuring seamless operations and effective communication.Diligently follow all documented policies and procedures including the company’s Compliance Program, FDA regulations and guidance, work schedules, breaks, and general attendance policies.Provide feedback and suggestions on potential areas of improvement within manufacturing and QC processes.

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