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Key skills for this role
Under the direction of a supervisor, performs a variety of tasks and operations that are required to support and execute the production of medical devices. This role focuses on developing, optimizing, and documenting manufacturing processes while supporting a collaborative production environment. This position will also work closely with Quality, Production, Manufacturing, and Engineering teams to ensure product consistency and regulatory compliance. Adherence to established Standard Work Instructions (SWI’s), Standard Operating Procedures (SOP’s), Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Quality Management System (QMS) is essential.
Under the direction of a supervisor, performs a variety of tasks and operations that are required to support and execute the production of medical devices. This role focuses on developing, optimizing, and documenting manufacturing processes while supporting a collaborative production environment. This position will also work closely with Quality, Production, Manufacturing, and Engineering teams to ensure product consistency and regulatory compliance. Adherence to established Standard Work Instructions (SWI’s), Standard Operating Procedures (SOP’s), Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Quality Management System (QMS) is essential.
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Expertise in primary manufacturing processes, fixture design, and tooling development, with a strong track record of optimizing production processes.
Extensive experience in supporting and improving a production environment, with a deep understanding of the operational requirements.
Advanced proficiency in SolidWorks CAD software for designing, modeling, and creating detailed technical drawings and simulations.
Proficient in operating and troubleshooting 3D Printing equipment and software.
Advanced proficiency with Microsoft Office applications.
Advanced proficiency with industrial engineering practices, including time studies, lean manufacturing techniques, and continuous improvement methodologies (LEAN/Six Sigma).
Strong ability to create, review, and update SWI’s, SOP’s, CC’s, and visual aids.
Strong ability to perform Non-Conformance investigations and CAPA root cause analysis.
Strong familiarity with FDA regulations, ISO 13485 standards, and other quality control practices relevant to medical device manufacturing.
Expertise with ERP systems and job traveler execution.
Strong analytical and problem-solving skills, with the ability to tackle complex engineering challenges.
Proven leadership in establishing and maintaining effective working relationships across teams and departments.
Demonstrated ability to work independently with a strong sense of urgency, and effectively under pressure.
Excellent written and oral communication skills.
Ability to stand for prolonged periods of time.
Ability to lift a minimum of 40 lbs.
High School Diploma, GED or equivalent required.
Bachelor’s degree in Manufacturing Engineering, Industrial Engineering, Mechanical Engineering, or related field required.
5 years of experience in manufacturing engineering role within the medical device industry preferred.
Parent group profile
EXALTA is a privately held orthopedic medical-device contract design and manufacturing group serving MedTech OEMs globally.
Visit parent group websiteFull-time
Senior · 5+ years experience
Onsite
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