Entry-Level QA Inspector: First Article (Med Device)

MillenniumSoft Inc; San Jose (CA); On-site; USD 28,000 - 34,000; Part time

Benefits offered by this job

Job summary

MillenniumSoft Inc is seeking a Quality Assurance Inspector (First Article Inspection) in San Jose, CA for a 6-month contract. The role focuses on visual and dimensional inspection of materials and products within the QA group, with emphasis on data entry, documentation accuracy, and adherence to SOPs.

The candidate should have 1–2 years of QA experience, familiarity with FAI, GMP/ISO 9000 standards, and strong attention to detail to ensure quality and compliance in a medical device context.

Qualifications

• 1-2 years of QA Inspector experience required or equivalent.
• Experience with First Article Inspection is required.
• Understanding of engineering change order processes.
• Good Manufacturing Practices (GMP) knowledge expected.
• Strong organizational and prioritization abilities.
• Detail oriented with ability to follow procedures precisely.

Responsibilities

• Perform visual and dimensional inspections per established criteria.
• Assess dimensional accuracy against drawings and specs with appropriate tools.
• Document review and data entry, ensure Good Documentation Practices.
• Record inspection results in SAP and communicate issues to engineers.
• Follow SOPs and contribute to continuous improvement.

Skills

Attention to detail

Communication skills

Problem solving

Multi-tasking

Organizational skills

Team oriented

Adaptable / Collaborative

GMP knowledge

Education

High School Diploma

Tools

SAP

Minitab

Blue Mountain Regulatory Management

Microsoft Office

Job description

MillenniumSoft Inc is seeking a Quality Assurance Inspector (First Article Inspection) in San Jose, CA for a 6-month contract. The role focuses on visual and dimensional inspection of materials and products within the QA group, with emphasis on data entry, documentation accuracy, and adherence to SOPs.

The candidate should have 1–2 years of QA experience, familiarity with FAI, GMP/ISO 9000 standards, and strong attention to detail to ensure quality and compliance in a medical device context.