When you join the team at Cordis, you become part of an inspiring mission to save lives, impacting millions of people and broadening access to life-saving cardiovascular and endovascular technology. As a global leader for over 60 years, we are dedicated to being the heart of innovation to transform cardiovascular care.

At Cordis, we're teammates, not just employees. We embrace an empowered and one-team culture where teammates are inspired to unleash their full potential. With diverse teams on a global scale, we believe the richness of our experiences and backgrounds enhances the careers of our teammates, the service to our customers, and ultimately, the lives of our patients.

If you love a challenge and are ready to have a direct, transformative and positive impact on the lives of millions, then Cordis is just the place for you.

We are the people behind the people who keep saving lives.

Summary

Adds value to the organization through expertise in process engineering and validation engineering, focused on implementing and managing changes derived from business and supplier needs. Responsible for planning, executing, and documenting tests to ensure that products, processes, and components comply with established technical, regulatory, and quality requirements.

• Evaluate and validate materials, components, and suppliers, ensuring technical and design compatibility.
• Develop and execute validation protocols to ensure compliance with internal and regulatory standards.
• Provide agile technical support to operations in areas such as problem resolution, directional changes, manufacturing scalability, process/product development, and material replacement.
• Manage and lead projects within their area or with external suppliers, ensuring a continuous supply of components for assembly lines
• Meet requirements related to quality, cost, delivery, and functionality, aligned with business objectives.

Responsibilities

• You should know and follow the policies and procedures of the company where he works related work activities in their area of ​​responsibility and ensure that subordinates know and follow company policies and procedures related to their work activities and area of ​​responsibility.
• Complete training in ​​responsibility within the allotted period. Training is required for changes and implementations of policies and procedures, new features, etc. Complete retraining required in areas such as safety and the environment.
• Follow all safety policies of the enterprise and safety precautions within the work area. Promote safety to all partners entering the work area.
• Responsible leadership and execution of projects focused on reducing the variation caused by process and / or product design to positively influence metrical business, strategic directions and financial results.
• Keep updated work plans for projects throughout the year as design changes in the core business (product line extension) products, process changes and cost improvement projects
• Identify and implement cost improvement projects to support the objectives of supply chain manufacturing and / or suppliers
• Managing technical projects at its manufacturing site and / or suppliers to improve the process of capacity, maintenance, instrument assembly capacity and performance of the instruments produced
• Provide technical support for the approval and validation of changes and process improvements in its manufacturing site and / or the supplier.
• Provide technical support for solving problems Quality of components
• Potentially coordinate monitoring activities in technical areas of MEST (Manufacturing Engineering Science and Technology) (RMI / CAD / BOM)
• Maintain the continuity of the supply chain qualifying and validating tools through the approval procedures of the components
• Secure closure of non-conformities of the problems of the components, in addition to their timely correction, in addition to the approval of plans of control within your area or suppliers.
• Those positions with supervisory responsibilities, will need to ensure his direct reports follows the company guidelines related to health, safety and environmental activities, and that the required resources to fulfill them are available and suitable for use. Responsible of purchasing and design equipment that complies with the safety and environmental requirements.

• It can serve as the lead engineer Operations in the development or review of a product of moderate complexity or have responsibility for multiple components or manufacturing process significant complexity in the development or review of a product. You can contribute with critical experience across multiple product lines. It may be responsible for the management and development of their technical support team.

  Plans, conducts and directs engineering projects or studies including complete projects that require an advanced level of knowledge in a specialized field. Apply a deep and diverse of engineering principles and practices within their assigned areas knowledge. You can coordinate and direct support activities and may be responsible for the technical development of the group assigned.

Required Qualifications

• Requires Engineering Bachelors Degree plus 5+ years of relevant experience.
• 4 to 6 years of experience in a validation environment, component evaluation, and/or manufacturing, or equivalent experience.
• Experience in the medical device industry is preferred.