What are the responsibilities and job description for the Manufacturing Engineer position at Datrose?
Job Details
We are seeking a Manufacturing Engineer to support our production operations. This role involves addressing production issues, generating quality documentation to demonstrate compliance, and driving cost reduction and productivity improvements. This individual will report to the Manufacturing Engineering Supervisor and will play a vital role in the sustaining and improvement of the production lines.
Position Responsibilities:
- Provide technical support for resolving production (floor) issues on medical X-ray equipment assembly and test lines.
- Generate and maintain quality documentation to ensure compliance with industry standards.
- Identify and implement cost reduction initiatives and productivity improvements.
- Collaborate with cross-functional teams to support new product introductions and process improvements.
- Contribute to defect investigations by determining root cause and executing corrective actions.
- Support engineering change management activities including component obsolescence, annual reviews, and supplier change activities.
Required Skills & Education:
- Must be able to work without the need for a VISA sponsorship.
- Bachelor's degree in Electrical Engineering, Electrical Engineering Technology, or similar
- Must have 3 years of experience in a manufacturing environment.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills.
- Ability to work collaboratively in a team environment.
- Proficiency with electrical test equipment and tools.
- Knowledge of typical quality expectations and compliance requirements.
- Ability to manage multiple tasks and prioritize effectively.
Position Expectations:
- This is a full-time, in-person role with typical hours from 7am - 4pm.
- The expectation is that this individual will be available while production is running.
Desired Skills:
- Experience with Lean Manufacturing and Six Sigma methodologies.
- Familiarity with industry standards and regulations (e.g., MDSAP, ISO, UL, CE).
- Comfortable navigating quality management in a medically regulated facility.
- Experience with engineering change management.
- Knowledge of cost reduction and productivity improvement techniques.
- Proficiency in MS Office Suite as well as Visio and Project.
- Experience with Design for Manufacturing (DFM) and Failure Mode and Effects Analysis (FMEA).
Work Environment:
- Manufacturing and office environments.
- Collaborative team setting focused on continuous improvement.
Physical Requirements:
- Ability to walk and stand for extended periods.
- Ability to lift up to 30 pounds.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
