QA Specialist, Implantable Medical Devices

Science; Paris; On-site; EUR 45,000 - 65,000; Full time

Job summary

Science is a clinical stage, vertically integrated technology company focused on neuroscience and unmet medical needs. The Quality Assurance Specialist will support the quality and conformity of implantable products throughout manufacturing, blending routine inspections with investigations to resolve non-conformances in a dynamic production environment.

Responsibilities include performing inspections, documenting in the QMS, CAPA involvement, and collaboration with audits and regulatory

Qualifications

• 2+ year diploma in quality, industrial processes or related field.
• 2+ years of quality control experience in medical devices or pharma manufacturing.
• Professional proficiency in English and French.

Responsibilities

• Perform incoming, in-process, and final inspections of medical device components and finished products.
• Conduct dimensional, visual, and functional testing using appropriate measurement equipment.
• Document inspection and test results in the Quality Management System.
• Identify and report non-conforming products and initiate corrective actions.
• Manage the Materials Review Board (MRB).
• Inspect product returns.
• Follow GMP and quality procedures.
• Participate in internal audits and support regulatory inspections.
• Ensure traceability of materials and products.
• Contribute to CAPA investigations and quality improvements.

Skills

Quality control

Documentation

Problem solving

English

French

Education

BTS/DUT Quality/Industrial Processes

Job description

Science is a clinical stage, vertically integrated technology company focused on neuroscience and unmet medical needs. The Quality Assurance Specialist will support the quality and conformity of implantable products throughout manufacturing, blending routine inspections with investigations to resolve non-conformances in a dynamic production environment.

Responsibilities include performing inspections, documenting in the QMS, CAPA involvement, and collaboration with audits and regulatory