Qualification Required

• Degree in Mechanical, Materials or Biomedical Engineering with years of experience

Roles And Responsibilities

• Manufacturing Engineering experience in Medical Devices.
• Hands on experience in Equipment/Process Validations IQ/OQ/PQ.
• Process improvements
• Sampling plan and Statistical Analysis.
• Vendor Coordination to source equipment.
• Fixture design, development, and verification.
• SOP (Standard Operating Procedure) create / update as needed.
• Manufacturing Procedure Documents
• Router Forms
• Experience on CAD (Solid works- Model & Drawings)
• Working independently with the internal and external stakeholders for execution.
• Provide leadership, training, and mentorship to less experienced team members.
• Demonstrated ability to manage and prioritize multiple tasks/projects with a strong problem-solving ability.
• Adhere to safety policy procedures.

Required Technical And Professional Expertise: IQ/OQ/PQ, Manufacturing, Medical Device, Process Validations, SOP, Vendor Coordination, Equipment Calibration