Process Validation & Manufacturing Engineer

Job Title:

Location: Warsaw, IN

Required Skills & Qualifications

Experience with process validation and regulatory compliance in the medical device industry

Engineering Documentation-Manufacturing Engineering 4-7 years Experience

Strong analytical skills and ability to compile and analyze data effectively

Excellent communication skills, both written and verbal

Ability to collaborate cross-functionally with various teams

Familiarity with FDA (21 CFR 820), ISO 13485, and other relevant regulations

Experience in continuous improvement initiatives and managing change controls

Preferred Skills & Qualifications

Familiarity with FDA (21 CFR 820), ISO 13485, and other relevant regulations

Experience in continuous improvement initiatives and managing change controls

Knowledge of various processing applications such as machining, finishing, forging, and molding

For immediate consideration please click APPLY to begin the screening process with Alex.