Key Responsibilities:
- Develop, implement, and maintain the company's quality management system in accordance with
relevant quality standards and regulations.
- Establish and monitor quality assurance procedures and processes to ensure product quality and
compliance with customer requirements.
- Manage and conduct inspections, tests, and audits to verify product quality and identify areas for
improvement.
- Collaborate with cross-functional teams, including production, engineering, and procurement, to
resolve quality issues and implement corrective and preventive actions.
- Conduct risk assessments and develop risk management strategies to mitigate quality-related risks
and ensure product safety and reliability.
- Drive continuous improvement initiatives to enhance quality performance, increase efficiency, and
reduce costs throughout the organisation.
- Monitor customer feedback and complaints to identify trends and opportunities for improvement and
implement measures to enhance customer satisfaction.
- Ensure compliance with relevant quality standards and regulations, such as ISO standards, FDA
regulations, and industry-specific requirements.
- Provide training and support to employees on quality assurance principles, techniques, and tools to
promote a culture of quality and excellence.
Qualifications:
- Minimum of 3 years of experience in quality management or a related role, preferably in the medical,
life science, or electromechanical manufacturing sectors.
- Strong knowledge of quality management principles, standards, and methodologies
(e.g., ISO13485, Six Sigma, Lean Manufacturing).
- Strong analytical and problem-solving abilities.
- Proven track record of driving continuous improvement and achieving results.