What are the responsibilities and job description for the Manufacturing Engineer II position at Grove Technical Resources, INC?
Job Title: Manufacturing Engineer II – Medical Device
Type: W2 Contract
Location: Onsite – Plymouth, MN
Summary:
Looking for a Manufacturing Engineer with 1–5 years of experience to support production operations, perform investigations, and ensure compliance in a medical device environment.
Key Skills:
• Root Cause Analysis & Investigations
• Technical Writing & Documentation
• Process Validation & Computer System Validation (CSV)
• Production Support & NCMR/CAPA Handling
• Strong Communication & Critical Thinking.
Nice to Have:
• Validation & performance analysis (MSA, IQ/OQ/PQ, TMV).
Responsibilities:
• Provide daily support on the production floor and resolve manufacturing issues
• Perform investigations, root cause analysis, and implement corrective actions (CAPA)
• Handle NCMR processing and ensure product quality compliance
• Develop and optimize manufacturing processes, layouts, and procedures
• Support validation activities and ensure adherence to regulatory standards
• Collaborate with cross-functional teams to improve efficiency and product performance
• Works independently with general supervision on moderately complex projects
• Contributes to process improvements and project milestones
• May mentor junior team members and support cross-functional initiatives.