Mechanical Engineer I

About the role

• Mechanical Engineer I
• Westborough, MA, USA, 01581
• 02/27/2017 to 02/25/2018 $28.37/hr on w2

Role Summary

A Mechanical Engineer 3 improves product design or designs new product using engineering principles and achieves expertise in mechanical engineering. The Mechanical Engineer 3 is responsible for running design controls and designing Mechanical product/subsystem release solutions.

Duties include (but are not limited to)

• Designing new products and/or supporting product quality improvement for disposable products for bioprocessing application.
• Executes design to engineering standards. Write design verification/validation plan, perform testing and write verification/validation report.
• Works within a team to deliver technical solutions.
• Works with technical leadership and cross functional team to ensure that the technical deliverables meet the product specification.
• Seeks mentoring to learn and solve problems
• Leading design visualization efforts with 3D CAD models and essential component and assembly details to explore multiple design options
• Developing engineering design concepts for components and disposable systems that have demanding requirements for regulatory compliance, reliability and cost
• Engaging in all phases of product redesign for improvement or new product development, including concept, prototype build, test, documentation, supplier interfaces, manufacturing introduction.
• Conducting analysis of existing and new product reliability using FMEA, risk management and DFR.
• Developing innovative designs to meet all requirements for performance, reliability, cost and manufacturability.
• Maintain and develop competence required for the job

Qualifications

• BS in Mechanical Engineering, Plastics, or Biomedical Engineering
• Knowledge in structural engineering, plastics molding, analysis, and verification of mechanical structures.
• Understanding in theories, concepts and techniques in structural and/or dynamics analysis
• Knowledge of industry and/or academic practices and standards related to structural analysis, finite element analysis, and structural verification testing, bioprocessing.
• Knowledge in statistics analysis, risk management and FMEA.

Quality Specific Goals

• Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position.
• Complete all planned Quality & Compliance training within the defined deadlines.
• Identify and report any quality or compliance concerns and take immediate corrective action as required

Characteristics

• Master’s degree in Mechanical Engineering, Biomedical Engineering or Plastics and 2 years relevant work experience
• Demonstrated design verification and validation and product design experience.
• Self-starter, energizing, results oriented, and able to multi-task
• Excellent teamwork, coordination and communication skills
• Ability to meet aggressive reliability, performance, cost, serviceability, and delivery targets
• Effective oral and written communication skills
• Global project experience

• Sandra Taylor
• Additional Information: Sandra Taylor