Job Description

Job Responsibilities:

• May assist with validation or troubleshooting of testing methods.
• • Routine assignments with limited judgment
• • Acquires job skills and follows company procedures
• • Works under close supervision
• Essential Duties and Responsibilities
• • Maintain and promote a safe work environment
• • Conduct inspections of in-process and finished goods
• • Record and maintain quality control documentation
• • Support investigations into non-conforming products
• • Support process audits for SOP and WI adherence
• • Initiate Non-Conforming Events (NCEs)
• • Review device history records and sales orders
• • Participate in Kaizen and continuous improvement initiatives
• • Complete training requirements and maintain records
• • Regular, punctual attendance and ability to work overtime
• • Exposure to mechanical parts, vibration, moderate noise
• • Safety shoes required in designated areas
• • May work with high voltage electronics, radiation, clean rooms, controlled environments, or dark rooms

Skills:

• • Basic Microsoft Office (Excel, Word, SharePoint, OneDrive)
• • Ability to follow written procedures
• • Effective written and verbal communication
• • Teamwork and independent work capability
• • High attention to detail
• • Use of QC tools (calipers, micrometers, gauges, microscopes, etc.)
• • Ability to read schematics and blueprints
• • Familiarity with GMP and GDP

Education/Experience:

• • Minimum: High School Diploma or GED
• • Associate Degree preferred
• Experience
• • 0–1 years preferred
• • Quality assurance or manufacturing experience beneficial
• • Experience in FDA-regulated medical device environment beneficial
• • Familiarity with Oracle ERP or Agile PLM beneficial

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