Junior Quality Manager - Regulatory Specialist
Yesterday
Description
• Lead the development and maintenance of Quality Management System (QMS). • Ensure compliance with regulatory requirements and standards such as ISO 13485 and FDA. • Manage relationships with partners for compliance and prepare regulatory submissions. • Provide training on quality-related topics across the organization. • Integrate QMS into the overall business strategy.
Requirements
• Bachelor's degree in engineering, science, or regulatory affairs. • Strong oral and written communication skills. • Ability to work independently and as part of a team. • Experience in quality management and regulatory affairs for medical devices is a plus.
Benefits
• The opportunity to impact the outcome of the company. • Interesting and challenging work. • Flexible working hours and minimal meeting culture. • A competitive remuneration.
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