Quality Control Manager M/F - NEWCLIP TECHNICS
Integrated into the Industrial Department, you will work under the responsibility of the Quality and Regulatory Affairs Department, which defines the orientations, quality requirements, and functional priorities of your activity.
Your missions will be as follows:
Steering Quality Control Activities
- Guarantee the performance of quality controls in compliance with regulatory requirements and the Quality Management System (QMS) procedures.
- Provide technical support to teams in the analysis and processing of non-conformities.
- Identify production drifts, alert stakeholders, and contribute to the implementation of corrective and preventive actions.
- Participate in the industrialization of new products by defining appropriate control methods and means.
Metrology and Control Means
- Manage the measurement equipment fleet (qualification, maintenance, calibration, verification, and renewal).
- Guarantee equipment availability by ensuring stock management, verification subcontracting, and procurement.
- Develop and deploy new control methods and means.
- Ensure the adequacy of control means with industrial and quality needs.
- Lead continuous improvement initiatives for control methods.
Quality, Continuous Improvement, and Performance
- Ensure the update of QMS documentation related to quality control and metrology.
- Participate in Statistical Process Control (SPC) and the monitoring of quality indicators.
- Contribute to the continuous improvement of quality control processes and the overall performance of the activity.
Management and Coordination
- Participate in the preparation and monitoring of the Quality Control activity budget in collaboration with the Quality and Regulatory Affairs Department.
- Collaborate closely with the Production, Quality, Industrialization, and Regulatory Affairs teams to guarantee product compliance and satisfaction of regulatory requirements.
Management and Activity Steering
- Manage, support, and develop the skills of a team of 12 employees.
- Organize, plan, and coordinate the activities of the Quality Control teams according to production priorities.
- Monitor the department's performance indicators and implement necessary improvement actions.
With a Master 2, Engineer, or equivalent degree, you have at least 3 years of experience in production quality control, ideally in the field of medical devices or micromechanics.
You master non-conformity management methods and root cause analysis tools, as well as the deployment of corrective and preventive actions. You are familiar with the main continuous improvement tools and know how to implement them in an industrial environment. You master metrology principles, control means, sampling techniques, and Statistical Process Control (SPC). You have a good knowledge of QMS and applicable standards, notably ISO 9001 / 13485. You have professional English skills, both spoken and written.
Rigorous, organized, and endowed with an excellent analytical mind, you know how to manage complex subjects. A field manager, you unite your teams and promote their development in a demanding industrial environment. Recognized for your interpersonal skills, diplomacy, and decision-making ability, you demonstrate discernment and know how to defend your quality requirements while maintaining constructive relationships with different departments.
Ready to join us? Join our innovative ETI showing 20% annual growth and evolve within an international company!
Newclip is committed to promoting diversity and inclusion in its recruitment. As such, this position is open to everyone, without distinction.
Our recruitment process: - Telephone exchange with the Recruitment team; - First HR interview; - Second interview with your future N+1; - Final optional interview with the Group Executive Director.