Summary: The QA Inspector III role at a medical equipment manufacturer involves ensuring product quality through daily inspections, monitoring production lines, and enforcing compliance with quality standards. The position requires adaptability to operate during Shift 3 hours, focusing on precision in product handling. The successful candidate will be responsible for documenting compliance and aiding in rework protocols as necessary. This role demands a strong understanding of quality assurance processes and adherence to Good Manufacturing Practices (GMP).

Key Responsibilities:

• Daily inspection of production lines documenting compliance on Daily Inspection Reports (DIR).
• Enforcing line clearance by inspecting work areas before use.
• In-process monitoring and sampling of finished products to assess quality.
• Aiding in rework protocols execution as needed with precise documentation review prior to QA release team submittal.

Key Skills:

• Mastery over overseeing ongoing processes within a live-production environment.
• Proficiently conducting Acceptable Quality Limit inspections.
• Strong ability using Laboratory Management Systems for logging samples or trials data crucial for process verification.
• Understanding GMP principles ensures adherence throughout testing phases to SOP's (Written instructions).

Salary (Rate): 60000

City: Nyack

Country: United States

Working Arrangements: undetermined

IR35 Status: undetermined

Seniority Level: undetermined

Industry: Other