Description
As a Systems Engineer Co-Op at Bayer Pharmaceuticals in Indianola, Pennsylvania, you will support product development projects within the Radiology Device R&D organisation.
Your tasks and responsibilities will include:
- Supporting systems engineering activities throughout the product lifecycle
- Assisting with requirements development, review, traceability, and change management activities
- Contributing to verification and validation planning, execution, data collection, and reporting
- Participating in engineering investigations and root cause analysis activities
- Assisting with risk management activities, including hazard identification, risk analysis, and risk control verification
- Contributing to human factors and usability engineering activities, including test preparation and analysis
- Analyzing test data and preparing engineering summaries and technical reports
- Supporting design reviews and cross-functional project meetings
- Working in laboratory and office environments to develop practical solutions to engineering challenges
- Supporting continuous improvement initiatives within the Systems Engineering organisation
- Assisting with technical documentation required for regulated medical device development
To be considered, you should:
- Be currently enrolled in an accredited bachelor's or master's degree program in Systems Engineering, Mechanical Engineering, Electrical Engineering, Biomedical Engineering, Chemical Engineering, Materials Science Engineering, or a related engineering discipline
- Have completed your sophomore year or higher
- Be able to work full-time during the Co-op assignment
- Possess strong analytical and problem-solving skills
- Be able to work effectively in a team environment
- Have effective written and verbal communication skills
- Be proficient with Microsoft Office applications, including Word, Excel, PowerPoint, and Teams
- Be able to organise and manage multiple assignments simultaneously
Preferred qualifications include:
- Laboratory or engineering project experience
- Coursework in medical device development
- Exposure to verification, validation, quality, reliability, or risk management concepts
- Familiarity with regulatory environments or standards-based development
In terms of compensation, employees can expect an hourly rate of approximately between $24.00 to $45.50, with additional compensation possibly including a bonus or commission, as well as benefits such as health care, vision, dental, retirement, PTO, and sick leave.
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