Quality Manager [Medical device]

  • Pulau Pinang
  • Permanent
  • Full-time
  • 29 days ago
We are currently looking for a Quality Manager for a leading player in the Medical Device Manufacturing Industry with a legacy of more than 40 years in the world. This position requires your urgent attention. Reporting to: Quality Director Based in Penang Attractive remuneration and benefits package the job Leads and develops a high-performing Quality Engineering team, ensuring alignment with customer needs, compliance standards, product quality goals, and risk mitigation strategies. Holds independent decision-making authority for product quality matters, including the disposition of non-conforming products. Drives functional and technical excellence, managing or supporting quality deliverables across product and process development initiatives. Participates in customer complaint investigations, ensuring timely and thorough resolution within their area of responsibility. Acts as a subject matter expert in QSR, ISO, and MDD standards, guiding quality-related decisions and promoting best industry practices. Leads quality planning and execution for major segments of complex projects, ensuring regulatory and organizational requirements are met. Approves and reviews validation, test, and operational data to define technical specifications and ensure consistent product performance. Champions continuous improvement by implementing new quality initiatives and enhancing the Quality Management System at the site and corporate levels. Mentors and develops staff, facilitating the adoption and understanding of quality initiatives and fostering a motivated, high-performance team culture. Collaborates cross-functionally on budget planning, EHS initiatives, and internal audits to support regulatory compliance and sustainability goals. the experience Bachelor of Science in Biomedical Science, Engineering, or a related field, or equivalent degree. At least 10 years of experience in a medical device production environment, including a minimum of 3 years leading a team. In-depth knowledge of ISO 13485 and 21 CFR 820 regulatory requirements. Strong skills in people management, problem-solving, risk management, and deviation/excursion handling. Familiarity with statistical methods and a basic understanding of financial principles is a plus. Show more Show less

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