Senior Quality Incoming/Process Supervisor

PowerToFly; France; Sur place; EUR 55 000 - 75 000; Plein temps

Résumé du poste

PowerToFly is seeking a Quality Control Manager in France who will lead quality control teams responsible for inspections and validations. The ideal candidate will ensure compliance with quality regulations and manage daily operations across manufacturing shifts.

Applicants should have a Bachelor's degree in Engineering and a minimum of 5 years of relevant experience, along with advanced proficiency in English and Spanish.

Qualifications

• Minimum 5 years of experience in Quality Engineering, Quality Control, or Quality Assurance.
• Minimum 2 years of experience leading or supervising quality personnel.
• Experience with corrective and preventive actions.

Responsabilités

• Lead and supervise Quality Control teams.
• Manage daily quality operations across shifts.
• Review and approve quality records and inspection results.

Connaissances

Strong knowledge of Quality Management System Regulations

Advanced English proficiency

Advanced Spanish proficiency

Experience in Quality Engineering

Formation

Bachelor’s degree in Engineering or a related technical field

Description du poste

What You Will Do

• Lead and supervise Quality Control teams responsible for incoming, in-process, and finished product inspections, document review, and validation testing.
• Manage daily quality operations across shifts to support manufacturing goals, product release timelines, and regulatory compliance.
• Review and approve quality records, inspection results, and batch documentation in accordance with established procedures.
• Coordinate product holds, product disposition activities, nonconformance investigations, and corrective action implementation.
• Monitor quality metrics and nonconformance trends to identify risks, drive process improvements, and support data-based decision making.
• Develop, train, and evaluate Quality Control personnel to ensure consistent execution of quality processes and procedures.
• Partner with Engineering, Manufacturing, and other functions to communicate quality requirements, provide training, and support product and process improvements.
• Support internal and external audits and maintain compliance with applicable quality system and regulatory requirements.

What You Will Need

Required Qualifications

• Bachelor’s degree in Engineering or a related technical field.
• Minimum 5 years of experience in Quality Engineering, Quality Control, or Quality Assurance within a regulated manufacturing environment.
• Minimum 2 years of experience leading or supervising quality personnel.
• Strong knowledge of Quality Management System Regulations, ISO 13485, and the Medical Device Single Audit Program (MDSAP).
• Advanced English proficiency, written and verbal.
• Advanced Spanish proficiency, written and verbal.

Preferred Qualifications

• Experience with corrective and preventive actions, nonconformance investigations, and root cause analysis methodologies.
• Experience supporting internal and external quality audits.