GMP QA Inspector - Medical Devices (Entry-Level)

Millenniumsoft; San Jose (CA); In loco; USD 28.000 - 34.000; Part-time

Descrizione del lavoro

Millenniumsoft in San Jose, CA is seeking an Entry-Level Quality Assurance Inspector for a 3-month contract on a W2 basis. The role focuses on visual and dimensional inspection of components and finished products within the QA group, with documentation verification and SAP recordkeeping.

You will work 40 hours per week on first shift, earning $20–$25 per hour. Requires US citizen or GC holder. GMP/ISO familiarization and attention to detail are essential.

Competenze

• Experience performing QA inspection and documentation review.
• Familiarity with GMP, FDA or ISO 9000 environments.
• Ability to read engineering drawings and specs.
• Knowledge of Good Documentation Practices.
• Ability to work under general supervision and in team settings.
• Strong verbal and written communication skills.

Mansioni

• Perform documentation verification and visual/dimensional inspection of materials and finished products.
• Assess dimensional accuracy using appropriate measurement tools and methods.
• Review documentation for completeness and compliance with standards.
• Record inspection results in forms or SAP, communicating issues to engineers.
• Follow SOPs and contribute to continuous improvement initiatives.
• Maintain a safe work environment and adhere to EH&S policies.

Conoscenze

First Article Inspection

Detail oriented

Read drawings

GMP/ISO 9000 awareness

Documentation review

Problem solving

Team oriented

Formazione

High School Diploma or equivalent

Strumenti

SAP

Minitab

MS Windows

Descrizione del lavoro

Millenniumsoft in San Jose, CA is seeking an Entry-Level Quality Assurance Inspector for a 3-month contract on a W2 basis. The role focuses on visual and dimensional inspection of components and finished products within the QA group, with documentation verification and SAP recordkeeping.

You will work 40 hours per week on first shift, earning $20–$25 per hour. Requires US citizen or GC holder. GMP/ISO familiarization and attention to detail are essential.