Responsibilities may include the following:

Provide day-to-day engineering support to manufacturing operations during 2nd shift activities.
Support production processes by investigating yield issues and implementing corrective actions.
Assist in engineering investigations related to nonconformances, product performance, and manufacturing deviations.
Participate in testing method development, troubleshooting, and validation support activities.
Support minor device redesigns and engineering changes to improve manufacturability and product performance.
Analyze customer returns and support root cause investigations and corrective/preventive actions.
Collaborate with suppliers and internal teams to support supplier-related changes and material evaluations.
Identify and implement cost optimization and process improvement opportunities.
Utilize statistical analysis and data trending tools to monitor manufacturing performance and support decision-making.
Support Lean Manufacturing and continuous improvement initiatives.
Prepare technical documentation, reports, and engineering records in compliance with company procedures and regulatory requirements.
Collaborate with Quality, Manufacturing, Supply Chain, and R&D teams to support operational goals.
Ensure compliance with GMP, quality systems, and applicable regulatory standards.
Other duties may be assigned.

Bachelor’s degree in Engineering.
1–3 years of experience in the medical device industry.
Strong analytical and problem-solving skills.
Knowledge of Lean Manufacturing and continuous improvement methodologies.
Yellow Belt or Green Belt knowledge preferred.
Ability to work in a team-oriented and fast-paced manufacturing environment.
Strong verbal and written communication skills in English and Spanish preferred.

Learn more about this Employer on their Career Site

Manufacturing Engineer I (2nd Shift)