Sr. Manufacturing Engineer

Responsibilities

• Demonstrating a primary commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all other documented quality processes and procedures.
• Providing technical assistance and leadership required to plan and implement projects to develop, install, and qualify new products, and/or new processes for manufacturing new products or for improving existing processes according to business plan objectives.
• Providing engineering input in the design, fabrication, development, installation, validation, and qualification of equipment/processes, which may include conducting feasibility studies and/or preparing proper documentation for project justification and training to ensure proper operation of the equipment.
• Leading cause-identification and problem-resolution for various types of production or service-related issues that arise.
• Monitoring and controlling programs, identifying issues, and ensuring they are resolved.
• Ensuring proper documentation is prepared or corrected to reflect any changes implemented.
• Researching and implementing cost reduction projects, lines, extensions, and/or products.
• Providing assistance to production as required.
• Planning work schedules, expenditures, attending meetings, and preparing monthly reports as required, ensuring effective communication of ideas, information, and issues to appropriate stakeholders.
• Assigning, delegating, and assisting in the completion of engineering tasks or projects to lower-level engineers.

• Bachelor’s degree in Engineering, Scientific discipline, or technical field;
  Master’s degree preferred.
• Minimum of 6 years’ experience in manufacturing or process engineering, or 5+ years with a Master’s degree in engineering, science, or a related technical field.
• Proven expertise in acquisition, validation, and support of automated manufacturing equipment.
• Hands-on troubleshooting and coding skills with PLCs and HMIs.
• Strong understanding of PLC/HMI signals, circuitry, and automated process control.
• Experience supporting High Volume automated production lines (10,000+ units annually), including process and equipment validation (IQ/OQ/PQ).
• Background in highly regulated industries such as medical devices, aerospace, pharma, or defense, familiar with ISO 13485 or similar standards.
• NO C2C CANDIDATES

JBL Resources is an Equal Opportunity Employer and E-Verify Company