Operational Quality Technician

Barrington James; Dijon; Sur place; EUR 40 000 - 50 000; Plein temps

Résumé du poste

A global leader in sports medicine in Dijon is seeking an Operational Quality Technician to contribute to quality operations and compliance with standards in a full-time role. You'll manage quality control activities, oversee validation processes, and work closely with various departments to ensure adherence to regulations. The ideal candidate has a technical degree, at least 3 years of experience in medical devices, and is fluent in French and English.

Qualifications

• 2-year degree (Associate level or higher) in Process Control, Industrial Engineering, or Quality.
• Minimum 3 years of experience in Operational Quality within Medical Devices.
• Fluency in French and English.

Responsabilités

• Perform or supervise in-process inspections, sampling, and identification.
• Prepare and oversee validation batch execution with the Production department.
• Lead the definition and implementation of information supply processes.

Connaissances

Interpersonal communication

Autonomy

Bilingual - French and English

Formation

2-year degree in Process Control, Industrial Engineering, or Quality

Description du poste

Barrington James is delighted to be partnering with a pioneering medical device company that is rapidly emerging as a global leader in the sports medicine space. This collaboration presents a unique opportunity to be part of a high-growth, innovation-led environment at the forefront of cutting-edge Class III medical advancements.

Our client is currently seeking a skilled Operational Quality Technician to join their team onsite in Dijon, France. This is a full-time, onsite role, offering the chance to contribute directly to the company’s quality operations and continued success.

General Mission / Purpose of the Position:

Your mission will be to contribute to Operational Quality activities to ensure compliance with applicable standards (Regulation 2017/745, ISO 13485, etc.).

Description of Activities:

• Production Quality Control: Perform or supervise in-process inspections, sampling, and identification;
• Prepare and oversee validation batch execution with the Production department;
• Lead the definition and implementation of information supply processes (Label printing, Instructions for Use);
• Lead the metrology monitoring activities of equipment;
• Manage non-conformities and the implementation of corrective and preventive actions (CAPA) related to products;
• Ensure monitoring and analysis of laboratory test results and participate in statistical data analysis;
• Participate in Supplier Quality activities related to the manufacturing of medical devices with relevant departments: Specifications, Approval, Integration, and Supplier performance monitoring, Non-conformity management;

Profile Requirements:

• 2-year degree (Associate level or higher) in Process Control, Industrial Engineering, or Quality;
• Minimum 3 years of experience in Operational Quality within Medical Devices
• Strong interpersonal skills to communicate with various stakeholders;
• Autonomous;
• Fluency in French and English

If this opportunity is of interest and aligns with your skills, please apply or send a copy of your up to date CV to [e-mail]