SITE TECHNICAL OPERATIONS MANAGER

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We are searching for the best talent for Site Technical Operations Manager to be in Juarez, a (Independencia) Responsible for managing all engineering functions for the manufacturing site.
Site primary products are Sutures and General Surgical Devices.
You will be responsible for.
Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position is responsible for the following.
· Create and institute career development programs, goals and objectives of subordinates in the engineering team · Plans, conducts and directs engineering project or studies including complete projects requiring advanced knowledge of a specialized field.
· Applies comprehensive and diverse knowledge of engineering principles and practices within broad assignment areas.
· Tracks and trends data identifies and implements process improvements to improve business measures.
· Develops engineering department goals and objectives and ensures targets are met.
· Ensure adherence to Quality System Regulation (QSR) and compliance to the quality policy in all activities.
· Ensure all OSHA and J& J Machine guarding requirements are met for new equipment and equipment changes as part of validation activities.
· Develops long and short-term strategic plans for the engineering organization and ensures adherence to plan · Ensure effective cost management of engineering operations · Manages the Capital budget and spending for the site.
· Support and promote the safety and industrial hygiene objectives of the plant · Pro-actively mitigates risks in processes and equipment.
· Responsible for validation and change control execution to meet associated procedures.
· Support diversity & inclusion · Collaborate and share best practices with Ethicon global engineering network, Technical Operations, PM, LCM, Ethicon sites, etc Qualifications · Strong PC experience required · Must have experience with process automation · Eight to ten years’ experience in manufacturing /design engineering · A minimum of BS, MS, or PhD in Engineering · P.
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License Desirable · BS, MS, or PhD in engineering discipline with experience or equivalent knowledge and skills to perform the position responsibilities.
· P.
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License Desirable · Position required excellent communications skills plus the ability to function in a team-based manufacturing environment.
· Must demonstrate a mastery of the analytical skills and professional judgment required to resolve major technical issues.
· Capable of creating effective management level presentations, writing formal reports dealing with both technical and business implications, and preparing project plans while identifying and understanding the interrelationships of related disciplines and key activities.
· Knowledge of working and supervising in an FDA /medical device regulated industry