Job Description
Qualifications
Minimum Qualifications – (Education, Experience, Certification, & Licensure):
- Bachelor’s Degree in Technical Engineering or a related field.
- Minimum of 3 years of experience, preferably in manufacturing or after sales service environment.
- Exposure to a regulated manufacturing or medical device environment preferred.
- Basic proficiency in Microsoft Office applications.
- Exposure to CAD software; experience or training in SAP/Power BI preferred.
Knowledge, Skills, and Abilities:
- Foundational knowledge of manufacturing and/or after sales service processes within a technical or regulated environment.
- Basic understanding of quality system principles, including documentation control, standard work, and change management.
- Ability to create, update, and maintain work instructions (written and graphically) in compliance with controlled documentation requirements.
- Ability to assist in developing basic test methods and performing required testing to troubleshoot processes and confirm process stability.
- Awareness of Lean Manufacturing and continuous improvement principles, with the ability to support improvement initiatives.
- Understanding of how production and service processes impact medical device performance, product quality, and end user outcomes.
- Strong organizational skills and attention to detail when working in regulated processes.
- Effective written and verbal communication skills suitable for cross functional collaboration.
- Ability to work effectively as part of a team in a fast-paced Production and Service environment.
- Demonstrated adaptability and willingness to learn new systems, equipment, and technical tools.
