דרושים ת.א.ג. כלים רפואיים בע"מ

1. Quality system Compliance: Ensure compliance with global regulatory requirements and standards for medical devices, including FDA QSR, ISO 13485, EU MDR, and others as applicable.
2. Design Control & Risk Management: Participate in design control activities, ensuring quality considerations are integrated into product development processes. Lead risk management activities (FMEA, risk analysis) to identify and mitigate potential issues.
3. Process Validation and Verification: Oversee the validation and verification of design and manufacturing processes. Ensure robust testing methodologies are applied to prove that designs meet all requirements and regulations.
4. Documentation and Records: Write and Maintain comprehensive documentation that meets regulatory and company requirements throughout the product development lifecycle. Ensure traceability and accessibility

Manufacturing engineer roll description:
1. Engineering POC for all production difficulties and improvements
2. Investigation of root cause for production problems
3. Design and manufacture production jigs.
4. Definition and improvement of the following:
i. Production process
ii. Assembly stages
iii. Packaging process
iv. Processing times
5. Process validation

Required Regulatory Affairs Specialist.