Director Of Quality Jobs

Director of Quality - Medical Device Contract Manufacturing (Metal Specialization)

Job Summary:

We are seeking an experienced Director of Quality to lead our Quality Assurance and Quality Control functions for medical device contract manufacturing with a specialization in metals. The successful candidate will be responsible for ensuring the quality of our products, processes, and systems, as well as ensuring compliance with all applicable regulations and standards. They will manage a team of quality professionals and work closely with other departments to ensure a high level of quality throughout the organization.

Responsibilities:

• Establish and maintain relationships with customers, suppliers, and regulatory agencies to ensure compliance with all applicable regulations and standards.
• Monitor and analyze quality metrics to identify trends and opportunities for improvement.
• Develop and implement quality policies, procedures, and standards to ensure that all products meet or exceed customer expectations and regulatory requirements.
• Provide leadership and guidance to the quality team, ensuring that they have the necessary resources and training to perform their duties effectively.
• Work closely with the sales and marketing teams to ensure that customer requirements are fully understood and incorporated into the quality management system.
• Collaborate with the engineering and production teams to ensure that quality is built into all products and processes.
• Provide regular reports to senior management on the state of the quality management system and any quality-related issues or concerns.
• Conduct regular audits and inspections to identify areas for improvement and ensure that corrective actions are taken promptly.

Requirements:

• At least 10 years of experience in quality assurance and quality control in the medical device industry, with a specialization in metal manufacturing.
• In-depth knowledge of quality management systems and regulatory requirements, including ISO 13485, FDA QSR, and MDR.
• Ability to work effectively in a fast-paced, dynamic environment.
• Proven experience in managing and leading a team of quality professionals.
• Excellent communication and interpersonal skills, with the ability to interact effectively with customers, suppliers, and regulatory agencies.
• Strong analytical skills and attention to detail.
• Bachelor's degree in engineering, quality assurance, or a related field; a Master's degree is preferred.

If you are a motivated and experienced quality professional with a passion for excellence and a desire to make a difference in the medical device industry, we encourage you to apply for this exciting opportunity.

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