Our client is seeking a highly skilled and experienced Senior Quality Specialist to join our Quality Assurance team. The ideal candidate will possess a deep understanding of quality engineering principles, regulatory requirements, and risk management processes applicable to the medical device industry.
This role requires a proactive individual who is capable of leading quality initiatives, driving continuous improvement, and ensuring compliance with both internal and external standards across cross functional teams.
PRIMARY OBJECTIVES & AUTHORITY :
- Implement and maintain quality management systems (QMS) in accordance with ISO 13485, FDA regulations, and other applicable standards.
- Lead root cause analysis and corrective action / preventive action (CAPA) investigations for non-conformities and quality issues.
- Collaborate with cross-functional teams to ensure quality considerations are integrated into product development and manufacturing processes.
- Perform internal audits and support external audits, ensuring compliance with regulatory requirements and company policies.
- Participate in Change Control process.
- Analyze quality metrics and trends to identify areas for improvement and drive continuous quality improvement initiatives.
- Provide training and guidance to team members
SKILLS, KNOWLEDGE AND EXPERIENCE :
- 5- 10 years’ experience as a Quality Specialist with strong knowledge and understanding of the practical implementation of ISO13485 and FDA CFR 21 part 820
- Strong QMS auditing skills
- Working knowledge of Good Manufacturing Practice (GMP)
- High level skills in using Microsoft Office Suite
EDUCATION / QUALIFICATIONS
- Bachelor’s in engineering, or equivalent qualification in engineering or a related scientific discipline
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