Quality Technical jobs

The Design Quality Engineering will be responsible for product and service quality planning, evaluation and control. Works cross-functionally in the development and implementation of prevention-based methodologies used in design, manufacturer, test, sustainability and correction of products and services.

Opportunity to join a fun company with cutting-edge products! This Supplier Quality group is growing rapidly as product lines grow - this is your chance to get in at the ground floor and make an immediate impact as a leader on the team!

The Quality Assurance Manager will be responsible for managing the Quality Management System to further continuous quality improvement. The Quality Manager will serve as the main point of contact for the quality team,

Michael Page is currently recruiting for a Sr. Quality Systems Manager to join a global pharmaceutical company located in Orange County.

Our client's Quality division is expanding and they're in need of a Quality Engineer with direct experiences within general quality functions - Quality Assurance/Quality Control, Quality Auditing, Quality Systems Management, all within the medical device industry. Not only will the right candidate have the ability to work on a highly unique product, but competitive compensation, a structured growth plan, and great benefits are also offered.

The Director of Quality - Aerospace will be responsible for supporting quality engineering requirements for new product development activities, customer quality approvals, production support and continuous improvement efforts ensuring continued certification to AS9100 Rev. D, ISO9001:2008, applicable Federal Aviation Administration (FAA) Regulations, and Department of Defense (DOD) Regulations.

The Quality Engineer is responsible for understanding customer quality related requirements, driving internal efforts for root cause and quality improvement, while supporting our high standards of precision and quality products in the inspection of medical parts.

Serving in a lead role, the Senior Manager, Regulatory Affairs -Medical Device will lead regulatory affairs submissions for product development globally. As the company sells products in new countries/regions and there are regulatory issues to navigate across the globe such as MDR requirements in Europe- which will be led by this person.

The Quality Engineer collects and processes data for quality improvement by identifying and implementing testing methods and statistical process control techniques. This individual is able to assess product reliability and process quality risks and make recommendations for design enhancements based on data in a collaborative environment.

The Quality Assurance Engineer will manage the CAPA (Corrective Action Preventive Action) process, as well as maintain high quality standards expected by customers in a rapidly growing market. Additional responsibility to lead ISO9001 Audits when necessary.

The Senior Quality Engineer is responsible for assuring manufacturing processes are in compliance with ISO Quality Management System to produce a consistent quality product. The Senior Quality Engineer will work day-to-day within the production environment to identify opportunities, support improvements, and reduce variation in our manufacturing processes resulting in improved product quality, delivery, and productivity.

A competitive candidate for this position would have working knowledge of quality systems, experience with AS9100, and someone who can be hands on within the manufacturing environment.

The Quality Manager is responsible for, but not limited to, ensuring that incoming and outgoing product quality meets the quality requirements as established by the division with its suppliers and its customer.

The Sr. Design Quality Engineering will be responsible for product and service quality planning, evaluation and control. Will oversee risk management processes and support new product development line.