FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.

Quality Inspector, 2nd Shift
HuFriedyGroup. Conduct component and assembly incoming, in-process, and final product inspections to appropriate standards using blueprints and inspection measurement equipment .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in conducting quality inspections and product testing in compliance with ISO 9001, ISO 13485, and FDA standards. Proficient in reading blueprints, generating documentation, and collaborating on problem-solving initiatives.
Highest-signal resume keywords
Quality InspectionBlueprint InterpretationDocumentation GenerationISO 9001 ComplianceFDA 21 CFR Part 820/211
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Quality InspectionProduct TestingBlueprint InterpretationDocumentation GenerationData EntryNonconformance ReportingCalibration Record ReviewProblem-SolvingAttention to DetailTechnical Analysis
Soft Skills
Good Communication SkillsTeam CollaborationAnalytical ThinkingDetail OrientationWritten Instruction Interpretation
Tools & Technologies
Inspection Measurement EquipmentProduction Qualification EquipmentLocal and Global Systems
Industry Keywords
ISO 13485MDSAPEU MDRFDA StandardsManufacturing EnvironmentQuality Experience
Tech Stack
Tools & technologiesAssembly
About the role
Key responsibilities & impact- Conduct component and assembly incoming, in-process, and final product inspections to appropriate standards using blueprints and inspection measurement equipment
- Perform product testing using various production qualification equipment
- Identify, segregate, and document rejected components and materials
- Participate on a Material Review Board to review and process nonconformance reports
- Enter and retrieve inspection and nonconformance data from local and global systems
- Review related quality documentation such as DHRs and calibration records
- Support local problem-solving activities and identify opportunities for improvement
- Complete other duties as assigned
Requirements
What you’ll need- 1-2 years' experience in a manufacturing environment and/or Quality experience
- Ability to read and interpret blueprints
- Ability to generate detailed, high-quality documentation
- Ability to work with others in analyzing and solving technical problems
- Attention to detail and ability to interpret written instructions
- Good communication skills (written and verbal) when working with others
- Must be able to perform quality inspection work under applicable ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, and EU MDR standards
Benefits
Comp & perks- Competitive salaries
- Comprehensive healthcare benefits
- Tuition assistance
- Generous paid time off
- Holidays
- Matching 401(k)
- Annual merit and incentive plans
- Vision
- Dental
- Quarterly bonuses
- 401K Match
- PTO
- Company Holidays