Sr Manufacturing Engineer

Grove Technical Resources, Inc.; Warsaw (IN); On-site; USD 95,000 - 135,000; Full time

Job summary

Grove Technical Resources, Inc. seeks a Sr. Manufacturing Engineer / Project Manager to lead EU MDR implementation activities at a manufacturing site in Warsaw, Indiana.

As the key liaison between Program Leadership and site teams, you will drive regulatory and manufacturing initiatives to successful completion. The role requires deep manufacturing experience, cross-functional leadership, and a focus on compliance and efficiency within a medical device environment.

Qualifications

• 7+ years of relevant experience in manufacturing engineering or a related field.
• Experience leading regulatory and change-control activities in manufacturing settings.
• Strong program/project management skills in a manufacturing environment.
• Cross-functional leadership across Quality, Engineering, Supply Chain and Operations.
• Regulatory compliance and risk management experience.
• Manufacturing readiness, documentation and system updates expertise.
• Master data management and process improvement exposure.
• Medical device industry experience preferred.

Skills

Project management

EU MDR

Change Control

ECO/MCO Implementation

Manufacturing Processes

Cross-functional leadership

Regulatory compliance

Master Data Management

Education

Bachelor's Degree in Engineering

Job description

Hiring: Sr Manufacturing Engineer (EU MDR Site Lead / Project Manager)

Location: Warsaw, Indiana

Duration: 12+ Months Contract

Type: W2 contract

Industry: Medical Device / Manufacturing

We are seeking an experienced Sr. Manufacturing Engineer / Project Manager to lead EU MDR implementation activities at a manufacturing site. This role will serve as the key liaison between Program Leadership and site teams, ensuring successful execution of regulatory and manufacturing initiatives.

Key Skills Required:

• Project / Program Management in Manufacturing Environment
• EU MDR, Change Control, ECO/MCO Implementation
• Manufacturing Processes & Operations Support
• Cross-Functional Leadership (Quality, Engineering, Supply Chain, Operations)
• Regulatory Compliance & Risk Management
• Manufacturing Readiness, Documentation & System Updates
• Master Data Management & Process Improvement
• Medical Device Industry Experience Preferred.

Requirements:

• Bachelor's Degree in Engineering
• 7+ years of relevant experience
• 5+ years in Project Management or Site Leadership roles
• Strong experience managing regulated manufacturing changes and meeting critical timelines.