Qualification/Validation Engineer

Barrington James Limited; Dijon; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A pioneering medical device company is seeking an Operational Quality Technician in Dijon, France. In this full-time, on-site role, you'll contribute to quality operations by overseeing production quality control, managing non-conformities, and collaborating with various departments. Ideal candidates should have at least 3 years of experience and a 2-year degree in a relevant field. Competitive environmental opportunities for career growth await you.

Qualifications

• Minimum 3 years of experience in Operational Quality.
• Strong interpersonal skills to communicate with various stakeholders.
• Organized, precise, and rigorous.

Responsabilités

• Perform or supervise in-process inspections and sampling.
• Lead problem-solving and continuous improvement meetings.
• Ensure monitoring and analysis of laboratory test results.

Connaissances

Production Quality Control

Problem Solving

Statistical Data Analysis

Interpersonal Skills

Formation

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

Description du poste

Overview

Barrington James is partnering with a pioneering medical device company in the sports medicine space. This collaboration offers a high-growth, innovation-led environment at the forefront of cutting-edge Class III medical advancements. The client is seeking an on-site Operational Quality Technician in Dijon, France. This is a full-time, on-site role contributing to quality operations and the company’s continued success.

Responsibilities

• Production Quality Control: Perform or supervise in-process inspections, sampling, and identification;
• Participate in product release activities to support the continuity of QARA service operations;
• 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;
• React to issues and lead problem-solving processes;
• 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;
• Supervise maintenance activities related to the Management of Material Resources.

Hierarchical / Project / Team Leadership Responsibilities

Lead meetings for problem-solving, continuous improvement, and change control.

Internal / External Working Relationships

• Internal: Collaboration with Production, R&D, and Quality/Regulatory departments;
• External: Suppliers, service providers, auditors, and consultants (non-exhaustive list).

Profile Requirements

• 2-year degree (Associate level or higher) in Process Control, Industrial Engineering, or Quality;
• Minimum 3 years of experience in Operational Quality;
• Confidentiality;
• Strong interpersonal skills to communicate with various stakeholders;
• Organized, precise, and rigorous;
• Autonomous;
• Adaptability.

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]