Manufacturing Engineer

Job Title: Manufacturing Engineer II – Medical Device

Type: W2 contract

Job Location: Plymouth, Minnesota (Fully onsite)

Duration: 6 months

We are hiring a Manufacturing Engineer to support production operations in a regulated medical device environment. This role focuses on process validation, root cause analysis, and production floor support to ensure product quality and compliance.

Key Skills Required:

Root Cause Analysis & Investigations

Process Validation (IQ/OQ/PQ) & CSV

Technical Writing & Documentation

Strong Communication & Organizational Skills

Production Support & Critical Thinking

Key Responsibilities:

Provide daily production floor support

Handle NCMR & CAPA investigations

Perform root cause analysis and implement corrective actions

Support process & computer system validations

Ensure compliance with quality and regulatory standards

Collaborate with cross-functional teams to improve manufacturing processes

Experience Required

1–5 years in manufacturing/medical device industry

Experience in validation and production support preferred