Quality Inspector

Integrated Resources Inc.; Littleton (CO); On-site; USD 50,000 - 75,000; Full time

Job summary

A premier staffing firm is seeking a Quality Inspector for a key role in ensuring compliance and quality standards within a regulatory environment. The ideal candidate will possess strong technical skills, experience in FDA/ISO settings, and the ability to lead and train others. This long-term position offers the opportunity to contribute significantly to quality assurance in a dynamic organization.

Qualifications

• Experience working in regulatory/FDA or ISO manufacturing settings.
• Certification in PCBA Inspection preferred.
• Proficiency in using calipers, microscopes, and pin gauges.

Responsibilities

• Ensure compliance with FDA and ISO/MDD regulations.
• Provide training and coaching for inspectors or production employees.
• Perform data collection and continuous improvement initiatives.

Skills

Proficiency in measuring and testing devices

Strong working knowledge of mechanical and electromechanical assemblies

Education

2-year Associate's Degree in a Technical Field

PCBA Inspection certification

Job description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-state area's most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy, and Nursing.

Job Description

Job Title: Quality Inspector – (2nd Shift - 1:00pm - 9:00pm)

Location: Littleton, MA

Duration: 2 Years

Position Description:

Uses a variety of technical precision measuring instruments to ensure acceptance and/or performance of components or finished devices according to established engineering instructions or quality practice standards. May provide training or job coaching to inspectors or production employees and works with independence of action and minimal supervision.

Responsibilities:

• Please note: Contractors are required to bring their own safety shoes.
• Follow all Quality System Practices and SOPs as defined by policies, practices, and procedures to ensure that FDA and ISO/MDD regulations are met.
• Participate within both departmental and cross-functional teams to assure compliance with regulatory and quality systems, including internal and external audits.
• Recommend and develop process, inspection testing, and procedural initiatives to support production and Quality Systems.
• Provide leadership and coaching to inspectors or production employees for inspecting and testing parts, finished goods, or re-worked items according to established specifications and testing methods; provide training as necessary.
• Ensure documentation of results, approve/reject items according to established standards.
• Ensure the accuracy of Quality Records for traceability according to established practices.
• Perform data collection, interpret and analyze information, and provide recommendations for solutions and continuous improvement.
• Demonstrate leadership and a service attitude throughout the organization.
• Identify and recommend training needs within manufacturing related to quality.
• Work within the framework of the Quality System.
• Collaborate with multifunctional teams, QA, or production.
• Comply with environmental, health, and safety site rules, policies, and governmental regulations.
• Perform other duties as assigned.
• Travel requirement: Less than 10%.

Qualifications

• Experience working in regulatory/FDA or ISO manufacturing settings.
• Proficiency in measuring and testing devices including calipers, microscopes, pin gages.
• 2-year Associate's Degree in a Technical Field or equivalent.
• PCBA Inspection certification (current or expired).
• Strong working knowledge of mechanical and electromechanical assemblies.