Product Manufacturing Engineer - On the Job Training

Qualifications and Experience:  

• Bachelor’s degree in Industrial Engineering, Mechanical Engineering, Manufacturing Engineering, or Mechatronics (or related field).
• 0–2 years of experience in manufacturing, quality, or product engineering environments.
• Basic understanding of manufacturing processes (assembly, injection molding, PCB integration, etc.).
• Familiarity with quality control concepts (IQC, in-process QC, final QC).
• Exposure to or willingness to learn PLM & QMS systems (preferably Arena).
• Strong attention to detail with ability to manage documentation and traceability.
• Good problem-solving skills with structured approach to issue investigation and root-cause analysis.
• Ability to work cross-functionally with engineering, suppliers, and quality teams.
• Interest in medical devices, wearable technology, and regulated product development.

Language Requirements

• English (fluent written and verbal) – Mandatory
• Arabic (fluent written and verbal) – Mandatory

This role owns the execution and management of Arena PLM & QMS systems, oversees manufacturing processes and quality control, and works closely with the NEXA Senior Product Engineer to monitor and guide manufacturers.

 The role also ensures that all manufacturing and quality activities align with medical regulatory requirements, maintaining full traceability, compliance, and product reliability.

• Review and validate manufacturers’ assembly, testing, and inspection processes to ensure alignment with NEXA requirements.
• Support manufacturing execution across DVT, PVT, and production, ensuring processes are followed and issues are tracked and resolved.
• Implement and maintain Arena PLM & QMS, ensuring accurate documentation, traceability, and control of product and quality data.
• Define and monitor IQC, in-process QC, and final QC, ensuring proper execution by manufacturers.
• Review manufacturing and validation test results from suppliers, ensuring accuracy, completeness, and compliance with NEXA requirements.
• Support root-cause analysis and CAPA activities, ensuring issues are properly investigated, resolved, and documented.
• Ensure all manufacturing and quality documentation (work instructions, process flows, inspection records, reports) are accurate and aligned with product revisions.
• Work closely with the NEXA Senior Product Engineer to identify manufacturing risks and support decision-making.
• Collaborate with the medical regulations team to ensure manufacturing and quality processes meet regulatory requirements.
• Communicate manufacturing and quality feedback to the product team to improve design, manufacturability, and reliability.