Quality Engineer

Capstan Medical, Inc.•Santa Cruz, CA

32d•Onsite

About The Position

The Product Quality Engineer is responsible for providing quality engineering support to the manufacturing line and supporting finished goods release for structural heart implant, delivery, and robotic devices. This role involves ensuring product quality throughout all stages of production in a cleanroom manufacturing environment, leading investigations into nonconforming materials and products, and ensuring compliance with regulatory requirements.

Requirements

Bachelor's degree in Engineering or a related technical field.
Knowledge of FDA regulations, ISO 13485, and other relevant quality standards for medical devices.
Experience working in a cleanroom manufacturing environment.
Experience with nonconforming material investigations and implementing effective CAPAs.

Nice To Haves

Master's degree is a plus.

Responsibilities

Provide quality engineering support to the manufacturing line and support finished goods release for structural heart implant, delivery, and robotic devices.
Collaborate with R&D and Regulatory Affairs teams to ensure that biocompatibility requirements are met for medical devices.
Provide guidance on sterilization processes and validations to ensure product safety and compliance.
Facilitate sterilization activities including batch release, sterilization validation, and coordination with third party sterilizers.
Oversee packaging validation activities to ensure product integrity and stability during storage and transportation.
Participate in finished goods release processes, ensuring compliance with release criteria and applicable regulatory requirements.
Oversee product quality during all stages of production in a cleanroom manufacturing environment.
Lead and support investigations into nonconforming materials and products (NCRs), working closely with cross-functional teams including Manufacturing and Engineering, identifying root causes, ensuring timely resolution, and implementing effective corrective and preventive actions (CAPAs) to prevent recurrence.
Participate in materials decision making as a member of Material Review Board.
Collaborate with cross-functional teams, including Manufacturing and Engineering, to resolve quality issues and identify opportunities for process improvement and efficiency gains within the manufacturing environment.
Perform audits of manufacturing processes, including inspections, testing, and documentation, to identify areas for improvement and ensure adherence to quality standards.
Maintain accurate and up-to-date documentation related to quality control processes, inspection results, metrology records, nonconformance reports, and corrective actions.
Ensure compliance with relevant regulatory requirements, such as FDA QSR and ISO 13485 standards.
Support internal and external audits, including preparation of documentation, participation in audits, and implementation of audit findings.