Description We are offering a contract to permanent employment opportunity for a Senior Engineer, Process Engineering in the Medical Devices industry based in Portage, Michigan, United States. The role involves a blend of technical expertise and project management, with a focus on PLC programming and validation work within a complex network of stakeholders.

Responsibilities:

• Provide engineering support for product transfers, ensuring all activities are completed and documented in compliance with the latest procedures.

• Determine the technical objectives of engineering assignments and make decisions that guide the direction and results of the assignment.

• Monitor and control progress of work, ensuring the sound application of engineering principles and appropriate use of policies and procedures.

• Analyze equipment to establish operating data, conduct experimental tests, and analyze results.

• May lead or act as an independent reviewer in process review meetings.

• Coach and mentor others on functionally related topics.

• Ensure quality of process and product as defined in the appropriate operation and material specifications.

• Select components and equipment based on analysis of specifications, reliability, and regulatory requirements.

• Work with quality engineers to develop component-specific testing and inspection protocols.

• Participate in the generation of internal process qualifications associated with product transfers, such as PFMEA, Control Plan, SOP, PPAP.

• Ensure adherence to safety procedures.

• Review and approve of validation documentation.

• Perform all other duties as assigned. Requirements • Must have strong management skills to oversee operations and project execution

• Proficient in creating and maintaining documentation related to system design, policies, and procedures

• Ability to plan, coordinate, and execute complex engineering projects

• Familiar with payroll systems and process in a large organization

• Demonstrated experience in quality review and assurance processes

• Exceptional design skills, especially in the context of process engineering in the medical devices industry

• Ability to troubleshoot issues, identify root causes and implement corrective actions

• Strong understanding of engineering principles and ability to apply them in a practical setting

• Excellent communication skills, both verbal and written, for effective interaction with stakeholders and partners

• Ability to collaborate effectively with cross-functional teams to achieve project objectives

• Proven experience in process improvement and optimization in a manufacturing environment

• Familiarity with component selection and specification in the context of medical devices

• Experience in developing and following engineering protocols

• Ability to prioritize tasks effectively to meet project timelines and quality standards. Technology Doesn't Change the World, People Do.®

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