manufacturing of medical prescription lenses. The QA Manager will work closely with cross-functional teams to promote continuous... judgment and decision-making abilities. Knowledge and experience in process validation (IQ, OQ, PQ, TMV). Certified...
manufacturing of medical prescription lenses. The QA Manager will work closely with cross-functional teams to promote continuous... judgment and decision-making abilities. Knowledge and experience in process validation (IQ, OQ, PQ, TMV). Certified...
experience on medical devices preferred. Experience in similar position (SQA) Visa Laser Demonstrate effective... control (SPC). Process Validation Activities skills (IQ/OQ/PQ), preferred. Strong working knowledge of Quality System...
of medical devices. This role drives continuous improvement initiatives using Six Sigma methodologies, establishes equipment... and execute equipment qualification protocols (IQ/OQ/PQ). Perform advanced troubleshooting and root cause analysis for complex...
leveling) in addition to high-energy short-form clips. Platform IQ: A deep understanding of the technical differences... & Context: High-level English comprehension to ensure captions are 100% accurate and medical/professional context is preserved...
About Convatec Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical...://www.convatecgroup.com Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical...
Qualtrics dashboards for various stakeholders ​Program Qualtrics Text iQ text analytics models to aide in both analysis... or veteran status, status as a victim of domestic violence, sexual assault or stalking, medical condition, genetic information...
About Convatec Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical.... Support on review IQ, OQ and PQ validations of test equipment validation. Safety, Health, and Environment Responsibilities...
using IQ/OQ/PQ Methodology by writing and developing Protocol Validations. Develop and maintain work instructions, quality.... Knowledge of medical device regulations/standards, including 21 CFR 820 (QSR) and ISO - 13485:2016 Experience - (Years...
such as Supplier pFMEA, FAIR, IQ/OQ/PQ validations, inspection reports, Gage R&R, and process capability analysis. Lead cross.... Experience in high-volume medical device manufacturing is a plus. Proficient in interpreting mechanical drawings (GD&T...