Cross-Functional, Detail Oriented, Document Management, Documentation, Documentation Review, Electricity, Engineering, Maintain Compliance, Manufacturing, Manufacturing Engineering, Manufacturing Systems, Mechanical Engineering, Medical Equipment, Process Flow, Process Validation, Risk Analysis, Risk Management, Standard Operating Procedures (SOP), System Integration (SI), Systems Engineering, Technical Writing, Writing Skills
Job Title: Manufacturing Engineer II
Location: Saint Paul, MN
Duration: 06+ Months
Shift Timings: Mon Friday 8:00am to 5:00pm
We are looking for a Manufacturing Engineer II to support quality system integration and manufacturing documentation activities for a leading medical device company.
Key Responsibilities:
- Review and update manufacturing procedures, SOPs, and qualification documents
- Support integration of legacy quality systems
- Maintain controlled process documentation, risk assessments, control plans, and process flow documents
- Execute and support equipment qualifications (IQ/OQ/PQ)
- Assist with line transfers, line duplication, or equipment moves
- Work cross-functionally with engineering and quality teams to ensure compliance and smooth execution
Required Skills:
- Strong documentation review and technical writing skills
- High attention to detail
- Experience with IQ/OQ/PQ documentation and execution
- General mechanical/manufacturing engineering knowledge
- Ability to work independently after training
- Prior experience with system integration projects
- Experience in medical device or regulated manufacturing environments
- Exposure to line moves, equipment transfer, or duplication projects
- Bachelor's Degree in Mechanical, Electrical, Software, or related Engineering field
- 3 5 years of relevant engineering experience preferred