MPE-Inc
Quality Inspector- $20-25/hour
At MPE we are dedicated to making a difference in the world through cutting-edge medical technology. Our mission is to be the global leader in design, engineering, and manufacturing solutions for the medical and technology industries. We are committed to creating impactful solutions that improve lives and fostering an environment where our team members can thrive, grow, and contribute to groundbreaking advancements in the medical field.
A better career for you. Creating medical technology for all.
We are seeking a dedicated Qualitynspector to join our team.
In this vital role, you will be responsible for ensuring products meet quality standards during the assembly process. Inspects products, documents findings, reviews production records, and works to identify and resolve any issues that arise during assembly.
If you enjoy working in a fast-paced environment where precision and teamwork matter, we’d love to hear from you!
Shift Available: Second Shift 2:30pm-11:00pm Monday-Friday
Key Responsibilities:
Conduct assembly line audits to verify proper equipment set-ups, availability of calibrated tools, and adherence to approved work instructions.
Reinforce Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) to production personnel.
Review each production records (DHR) for completeness, accuracy, and legibility; ensure all records are scanned or otherwise archived per Quality System requirements.
Execute product release — including completion of independent final inspections, sign-offs, and system transactions to authorize shipment of conforming assemblies.
Evaluate nonconforming material, coordinate disposition activities, and document investigations/dispositions per Quality System requirements.
Participate in assembly line validations by collecting objective evidence and documenting results for approval.
Maintain operator training records and ensure personnel are qualified prior to performing assembly tasks.
Issue quality alerts to production personnel for complaints and nonconformances to prevent recurrence.
Document process deviations and in-process changes for applicable approvals
Provide Process Engineering information on work instruction and process gaps for continuous improvement
Support evaluation and documentation of rework for assemblies (including product returns) per Quality System requirements.
Qualifications
Education:
High school diploma or equivalent required.
Experience and Training:
1-2 years of experience in a manufacturing environment (preferably device assembly)
Blueprint reading
Use of measurement tools
Material Review Board (MRB) and Nonconformance management
Intermediate-level Geometric Dimensioning & Tolerancing (GD&T)
Familiarity with Good Documentation Practices and production record review
Proficiency with Microsoft Outlook and Microsoft Excel
Broad understanding of materials, manufacturing technologies and processes preferred
Proficiency with electronic ERP systems and inspection management systems preferred
Physical and Mental Demands:
Regularly required to visually inspect parts, use computers, problem solving and troubleshooting
Must be able to read blueprints
Specific abilities include close vision, colored vision
Why Join Us?
Mission-Driven Work: Help deliver medical products that change lives.
Growth Opportunities: We support career development and internal promotions.
Comprehensive Benefits:
Medical (HSA-qualified and traditional plans), dental, and vision—coverage starts the first of the month after hire.
401(k) with company match.
Nine paid holidays and vacation time from day one.
If you're detail-oriented, team-driven, and ready to contribute to life-changing medical technology, apply today and grow your career at MPE.
No relocation or sponsorship available for this role.
At MPE we are dedicated to making a difference in the world through cutting-edge medical technology. Our mission is to be the global leader in design, engineering, and manufacturing solutions for the medical and technology industries. We are committed to creating impactful solutions that improve lives and fostering an environment where our team members can thrive, grow, and contribute to groundbreaking advancements in the medical field.
A better career for you. Creating medical technology for all.
We are seeking a dedicated Qualitynspector to join our team.
In this vital role, you will be responsible for ensuring products meet quality standards during the assembly process. Inspects products, documents findings, reviews production records, and works to identify and resolve any issues that arise during assembly.
If you enjoy working in a fast-paced environment where precision and teamwork matter, we’d love to hear from you!
Shift Available: Second Shift 2:30pm-11:00pm Monday-Friday
Key Responsibilities:
Conduct assembly line audits to verify proper equipment set-ups, availability of calibrated tools, and adherence to approved work instructions.
Reinforce Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) to production personnel.
Review each production records (DHR) for completeness, accuracy, and legibility; ensure all records are scanned or otherwise archived per Quality System requirements.
Execute product release — including completion of independent final inspections, sign-offs, and system transactions to authorize shipment of conforming assemblies.
Evaluate nonconforming material, coordinate disposition activities, and document investigations/dispositions per Quality System requirements.
Participate in assembly line validations by collecting objective evidence and documenting results for approval.
Maintain operator training records and ensure personnel are qualified prior to performing assembly tasks.
Issue quality alerts to production personnel for complaints and nonconformances to prevent recurrence.
Document process deviations and in-process changes for applicable approvals
Provide Process Engineering information on work instruction and process gaps for continuous improvement
Support evaluation and documentation of rework for assemblies (including product returns) per Quality System requirements.
Qualifications
Education:
High school diploma or equivalent required.
Experience and Training:
1-2 years of experience in a manufacturing environment (preferably device assembly)
Blueprint reading
Use of measurement tools
Material Review Board (MRB) and Nonconformance management
Intermediate-level Geometric Dimensioning & Tolerancing (GD&T)
Familiarity with Good Documentation Practices and production record review
Proficiency with Microsoft Outlook and Microsoft Excel
Broad understanding of materials, manufacturing technologies and processes preferred
Proficiency with electronic ERP systems and inspection management systems preferred
Physical and Mental Demands:
Regularly required to visually inspect parts, use computers, problem solving and troubleshooting
Must be able to read blueprints
Specific abilities include close vision, colored vision
Why Join Us?
Mission-Driven Work: Help deliver medical products that change lives.
Growth Opportunities: We support career development and internal promotions.
Comprehensive Benefits:
Medical (HSA-qualified and traditional plans), dental, and vision—coverage starts the first of the month after hire.
401(k) with company match.
Nine paid holidays and vacation time from day one.
If you're detail-oriented, team-driven, and ready to contribute to life-changing medical technology, apply today and grow your career at MPE.
No relocation or sponsorship available for this role.