Quality Assurance Specialist

The Quality Specialist will be responsible for developing, implementing, and maintaining quality assurance processes to guarantee the delivery of top-notch products or services to our customers.

Main Responsibilities:

• Develop and implement quality assurance policies and procedures to ensure compliance with industry standards and regulations.
• Collaborate with cross-functional teams to establish and enforce quality control measures throughout the production process.
• Create and maintain comprehensive documentation related to quality standards, processes, and procedures.
• Generate detailed quality reports and performance metrics to track key indicators and trends.
• Communicate findings and recommendations to relevant stakeholders, ensuring transparency and accountability.
• Investigate and analyze quality issues, customer complaints, and non-conformances to determine root causes.
• Collaborate with relevant departments to implement corrective and preventive actions to address identified issues.
• Provide training to employees on quality control processes, standards, and best practices.

Qualifications & Requirements

• Bachelor’s degree in a related field (e.g., Quality Management, Engineering) or equivalent work experience.
• Proven experience in quality assurance in the medical device industry.
• Keen business approach to problem solving and decision making while effectively managing multiple priorities simultaneously.
• Strong knowledge of quality management systems and methodologies.
• Excellent analytical and problem-solving skills with a keen attention to detail.
• Effective communication and interpersonal skills, with the ability to work collaboratively across departments.
• Thorough understanding of and commitment to complying with all applicable laws regulations and industry standards.
• Proficient English level reading, writing and verbal skills.
• Certification in quality management (e.g., CQE) is a plus.