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Senior Safety Health

3 months ago

Stanmore, Greater London, United Kingdom Cpl Full time

CPL are seeking a dedicated, experienced and hands on Quality Lead to join a Medical Devices organisation in Sunbury. Reporting to the Head of Quality and Regulatory Affairs, the Quality Lead will be responsible for the implementation of all aspects of the company's quality management system to ensure compliance with industry standards, regulatory requirements, and customer specifications. The successful candidate will have a proven track record of implementing and maintaining effective quality assurance processes and driving continuous improvement initiatives.

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 organization.


• 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:


• Bachelor's degree in a relevant field (e.g., Quality Management, Engineering, or related discipline).


• 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).


• Experience in developing and implementing quality management systems and processes.


• Excellent communication, and interpersonal skills.


• Strong analytical and problem-solving abilities.


• Proven track record of driving continuous improvement and achieving results.


• Certification in quality management (e.g., Certified Quality Manager, Six Sigma Black Belt) is a plus.

Benefits:


• Competitive Salary + 5% annual bonus


• 6% Pension, EAP. Medical top up scheme, Income Protection Policy, Group Life assurance


• 25 days holiday pa + Bank holidays