Mechanical Manufacturing Engineer I (3104)

MEVION MEDICAL SYSTEMS INC•Littleton, MA

3d•$85,000 - $95,000•Onsite

About The Position

Mechanical Manufacturing Engineer I supports manufacturing operations by sustaining, implementing, and improving production processes for mechanical components and assemblies. This entry-level role focuses on process execution, documentation, troubleshooting, and continuous improvement while building foundational manufacturing engineering skills.

Requirements

Bachelor of Science degree in Mechanical Engineering (or equivalent). Advanced degree is desirable.
2+ years of experience as a Manufacturing Engineer (or equivalent) with regulated environment experience preferred.

Nice To Haves

Familiarity with manufacturing and continuous improvement tools (e.g., Six Sigma, SPC).
Strong analytical and problem-solving skills.
Working knowledge of quality systems, NCR processes, and root cause analysis methods (e.g., 5 Whys, Fishbone).
Ability to read and interpret mechanical drawings; basic understanding of GD&T.
Experience with common manufacturing processes, including fabrication, machining, and mechanical assembly.
Familiarity with CAD software (e.g., SolidWorks).
Knowledge of tooling and mechanical assembly techniques for multi-component systems.
Ability to work effectively in cross-functional teams with strong written and verbal communication skills.

Responsibilities

Support existing manufacturing processes to ensure safe, efficient, and quality production.
Maintain and update manufacturing documentation, including work instructions, process flows, Bills of Material, inspection criteria, and other controlled documents.
Support investigation, documentation, and timely processing of Non-Conformance Reports (NCRs), including data collection, review of drawings/specifications, and coordination with Quality and Engineering.
Assist in troubleshooting production issues and participate in root cause analysis and corrective action activities related to manufacturing and NCR findings.
Support implementation of Engineering Change Orders (ECOs) and controlled document updates.
Collaborate with production, quality, and supply chain teams to resolve routine manufacturing challenges.
Participate in data collection and basic analysis to support process monitoring and improvement efforts.
Support prototype builds, pilot runs, and validation activities as assigned.
Assist with non-conformance investigations and corrective action activities.
Follow established safety, quality, and regulatory requirements.
Perform other related duties as assigned.