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You will participate in selecting and qualifying suppliers and ensure that they deliver quality parts, components, and materials. You will also be evaluating suppliers' internal functions.
In this role you will be in charge of overseeing and managing quality control processes related to product design. You will ensure compliance with regulatory standards, conducting risk assessments, and leading cross-functional teams in the development and implementation of quality management systems.
In this role you will focus on maintaining and improving product quality within the manufacturing process. Responsibilities include assisting in developing and implementing quality management systems, conducting risk assessments, and collaborating with cross-functional teams to address quality issues and drive continuous improvement.
In this role you will be overseeing and implementing quality control processes to ensure compliance with regulatory standards and maintain product excellence. Responsibilities include developing and implementing quality management systems, conducting risk assessments, and collaborating with cross-functional teams to address quality issues and drive continuous improvement.
The Quality Engineer 3 position with my client involves ensuring adherence to quality standards and regulatory requirements in the production of medical devices and pharmaceutical products. Responsibilities include conducting quality assessments, implementing corrective actions, and collaborating cross-functionally to drive continuous improvement in product quality and reliability.
The Design Quality Engineer role involves ensuring the quality and compliance of medical device designs, particularly in organ preservation and transplantation. Candidates will apply expertise in quality management systems and regulatory standards to drive product safety and efficacy in this critical healthcare field.
The Senior Quality Engineer will enhance awareness, visibility, and communication regarding quality initiatives while supporting departmental, functional, and corporate quality goals within a medical device manufacturing space. The ideal candidate will possess a robust understanding of FDA/ISO 13485 Quality System requirements, GxP standards, and other pertinent regulations.
Step into the role of Senior Quality Assurance Specialist, where you'll leverage your extensive experience to ensure adherence to the highest quality standards and regulatory compliance within the dynamic field of medical devices. As a key player, you'll spearhead initiatives aimed at driving innovation and advancing patient care through meticulous attention to detail and a commitment to excellence.
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