
Program Manager
- Mexicali, B.C.
- Permanente
- Tiempo completo
- Develop and manage long term goals and translate them into shorter projects to achieve the success of the programs.
- Prepares justification for the programs being managed, such as budget, ROI, etc., to achieve buy in from top management.
- Plan, organize track and lead execution of high scope/impact projects.
- Identify potential risks and develop
- Lead and organize project reviews affecting the Mexicali site.
- Prepares status reports for the projects and programs being lead and present at an executive level.
- Develop and maintain budget estimates/control for programs and projects.
- Ensure proper documentation is prepared and updated to meet standards and regulations as required in a medical device environment (FDA/ISO).
- Have the ability to influence others to perform needed tasks to ensure project completion on time and within budget.
- May require coaching other engineers in project management tools.
- Ability to lead cross functional, multisite and multicultural (both US and MX) teams.
- Performs other duties as required.
- Travel: Position may require 10-30% travel depending on the project, primarily within U.S
- Be of high character and energy with regard for detail.
- Schedule oriented and demonstrate results based on such schedules (Plans / Gantt charts)
- Highly organized with his/her tasks and tasks related to his/her programs.
- Excellent communication skills, both written and verbal. Able to communicate eloquently up, down, and sideways within the company.
- Possess strong communication skills to interact with suppliers and other departments within the company (product development, planning, purchasing, regulatory, quality, etc.).
- Demonstrate strong leadership skills to coordinate cross functional and/or multisite/multicultural teams for his/her program.
- Demonstrate sites bring up and sites transfer knowledge and experience.
- Minimum 4 years in a Project/Program Manager role or an engineering leading role.
- Minimum 6 years mechanical, manufacturing or process engineering experience with Mid/high volume complex mechanism manufacturing.
- BS degree in Industrial/Mechanical/Electrical/Electronic Engineering or equivalent.
- High English Level (+ 90 %).
- None
- MS in an engineering or administration discipline.
- Project Management Certification.
- Prior demonstrated responsibility for product, process or equipment validation / verification.
- Prior experience with automated equipment, complex manufacturing mechanisms or robotics.
- Experience in Just-In-Time, Demand Flow Technology, and Lean Manufacturing techniques.
- Prior experience working in an FDA/ISO regulated environment.