Sr. Engineer I - Interim Assignment in Maryland

Job Summary

This position will be located temporarily on-site in Elkton, Maryland for 18-24 months, then transferred to Ann Arbor, Michigan. This position is responsible for investigating, planning, and implementing complex improvements in and/or additions to current products and manufacturing processes that directly affect safety, quality, regulatory compliance, and productivity. Involved with leading projects requiring engineering team effort or a multidiscipline team effort.

Responsibilities

• In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
• Provide 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.
• Provide engineering input in the design, fabrication, development, installation, validation, and qualification of equipment / processes which may include feasibility studies and/or proper documentation for justification of project and training to ensure proper operation of the equipment.
• Lead cause-identification and problem-resolution for various types of production or service-related issues that arise.
• Monitor and control programs, identify issues and ensure they are resolved.
• Ensure proper documentation is prepared or corrected to reflect any changes implemented.
• Research and implement cost reduction projects, lines, extensions, and/or products.
• Provides assistance to production as required.
• Plan work schedules, expenditures, attend meetings, and prepare monthly reports as required, ensuring effective communication of ideas, information, and issues to appropriate stakeholders.
• Assign, delegate, and assist in the completion of engineering tasks or projects to lower level engineers.
• Perform other duties as assigned.

Qualifications

• Requires a four-year college degree in an engineering, scientific, or technical discipline and a minimum of six years of experience within a engineering environment or a Master's degree in an engineering, scientific, or technical discipline and a minimum of five years of experience in an engineering environment.
• Intermediate computer software skills, i.e. Microsoft Office.
• Experience in medical device industry preferred.
• Minimum three years experience in the acquisition, validation and support of Automated Manufacturing Equipment.
• Ability to edit and troubleshoot PLC and HMI code.
• Experience with Omron systems preferred.

Benefits

• 401(k) with 6% matching
• Paid time off
• Company paid holidays
• Medical, dental, vision insurance
• Flexible spending account
• Health savings account
• Company paid life insurance
• Employee assistance program
• Parental leave
• Tuition reimbursement