Linkedprime
Confidential

Jr Projects and Process Engineer

Posted: 13 hours ago

Job Description

Contributes with the definition, implementation and execution of the tactical tasks defined by the Global Operations Support Group about the Global Molding strategy and will support the drafting of technical validation documents for software or equipment to be installed in the sites of the Medical Devices Group.Essential Duties/ Responsibilities and Tasks:Participate of projects definition at a broad level beginning with a business case to assure that the project is feasible. If the approval is obtained, project charter or project initiation documents must be issued where the purpose and requirements of the project are expressed.Understand the scope of the project and the goals that will be achieved as part of the project implementation.Help to develop a project management plan that includes the identification of costs, quality and resources, and the project timeline.Understand the risk associated with the implementation and the action plan for mitigation actions to countermeasure the potential impacts. The knowledge of the product and process system allows an effective risk identification.Execute the communication plan for internal and external stakeholders.Lead the periodic project meetings.Provide report outs at least once a month.Develop, write, and support validation documents for new or actual equipment and/or software in collaboration with cross functional teams by design and writing engineering studies, validation protocols and test cases.Asure compliance with FDA Quality System Regulation and Moog’s standards related to good documentation practices.Review and approval of technical content within the Moog’s document management system.Supporting global cross-functional development and/or sustaining projects.Identify compliance gaps and work with Engineering to resolve compliance issues.Support cross-functional projects to improve and maintain compliant, effective, and efficient quality processes.Maintain up-to-date knowledge of regulatory requirements, international standards, and company QMS procedures for areas of responsibility.Education and/or experience:BS in Mechatronics, Electronics or a closely related discipline from an accredited university.

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