Manufacturing Engineer

Company Description

Incipio Devices is an orthopedic device company focused on solution‑driven approaches to contract manufacturing, and contract development. The organization partners with customers to design and produce high‑quality orthopedic devices that meet stringent performance and regulatory expectations. Team members work in a collaborative environment that values innovation, precision, and reliability in medical device manufacturing. Applicants can expect to contribute to products that support better outcomes for patients and healthcare providers.

Additional information about the company and its product portfolio is available on the Incipio Devices website.

The Manufacturing Engineer is a full‑time, on‑site role based in Huntington, IN. This role is responsible for developing, improving, and supporting manufacturing processes for orthopedic devices, with a focus on safety, quality, and efficiency. Day‑to‑day activities include designing and optimizing process flows, creating and maintaining work instructions, and collaborating with engineering, production, and quality teams to resolve manufacturing issues. The Manufacturing Engineer will analyze production data, implement continuous improvement initiatives, and support cost‑reduction and yield‑improvement projects.

Additional responsibilities include evaluating and specifying equipment and tooling, supporting validation and qualification activities, and ensuring compliance with applicable medical device manufacturing standards and regulations.

• Strong foundation in Manufacturing Engineering and Manufacturing Processes, with experience developing and optimizing production methods.
• Background in Mechanical Engineering and Industrial Engineering, with the ability to apply engineering principles to process design and problem solving.
• Hands‑on experience with Machining and related manufacturing techniques, including understanding of tooling, setup, and process parameters.
• Bachelor’s degree in Mechanical, Manufacturing, Industrial Engineering, or a related technical field (or equivalent practical experience).
• Experience in medical device or other regulated manufacturing environments is preferred.
• Proficiency with CAD and basic design interpretation (e.g., GD&T, drawings, specifications).
• Demonstrated skills in root cause analysis, continuous improvement, and lean or similar methodologies.
• Effective communication and teamwork skills, with the ability to collaborate across production, quality, and engineering teams.
• Strong organizational skills, attention to detail, and the ability to manage multiple projects and priorities in a fast‑paced environment.