Industrialization and Engineer Transfer (H/F)

Stilla Technologies

Villejuif

Sur place

EUR 45 000 - 55 000

Plein temps

14 jours+

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Résumé du poste

A leading biotechnology company in Villejuif is seeking an Industrialization and Transfer Engineer to join their team. The role involves transferring and supporting product development, particularly the QX700™ machine, within a multi-disciplinary environment. Candidates should have a strong engineering background with at least 5-8 years of experience in relevant fields, project management skills, and the ability to communicate effectively in both French and English. Compensation ranges from 45,000 to 55,000 EUR based on experience.

Qualifications

5-8 years minimum in electrical, mechanical engineering within biotech, medtech, diagnostics, or microfluidics.
Experience in transfer activities is ideal.
Familiar with ISO 13485, GMP-like systems.

Responsabilités

Define industrial specifications and project framework.
Coordinate transfer phases and ensure product compliance.
Drive continuous improvement initiatives.

Connaissances

Strong engineering background

Advanced analytical expertise

Solid experience in Control design

Regulated environment expertise

Project management experience

External communication

Team spirit

Fluent in French

High-level English

Formation

Master’s degree / Engineer degree

Description du poste

Overview

Stilla Technologies is a Paris-based European biotechnology company that focuses on accelerating the development of next-generation genetic tests by providing biologists with tools for high-resolution genetic analysis. Stilla Technologies was founded in 2013 and is now part of Bio-Rad Laboratories as LSG-Paris entity. Since 2016, Stilla Technologies/Bio-Rad LSG-Paris provides research organizations specialized in molecular biology and genetic analysis. LSG-Paris has developed a range of digital PCR instruments (Naica®, Nio® and QX700™ systems), which, with microfluidic chips, dedicated reagents, and advanced data analysis software, enable analysis of many genetic biomarkers (multiplexing) with high sensitivity and precision. This technology supports new precision genetic tests in applications such as liquid biopsy, pre-natal testing, Gene Therapy, infectious disease, and GMO detection. Our multi-disciplinary teams in microfluidics, mechanical engineering, biology, and software build Life Science Products based on deep technological innovation. We aim to empower scientists with pioneering digital PCR solutions to advance genetic testing.

Position

We are currently looking for an Industrialization and Transfer Engineer to join the Transfer and Industrialization team (TnOP) within the Manufacturing Operations department. This role focuses on transferring and supporting external LSG-Paris products, especially the QX700™ machine and linked products. The role operates within a cross-functional and multi-disciplinary environment, requiring a comprehensive understanding of the entire system (machines, reagents, consumables).

Key Missions

Definition of industrial specifications and project framework
Establish a specifications document based on technical (R&D), marketing, quality and regulatory, and logistics requirements; evaluate and select suppliers or subcontractors according to Quality / Cost / Time / Reliability criteria
Establish the schedule and budget for the prototype-to-industrial-product transfer phase
Coordinate transfer phases
Plan the production of industrial batches, define sampling and control criteria (incoming, in-process, final, maintenance); ensure products meet industry standards and customer needs
Evaluate batch compliance and industrial performance (reproducibility, repeatability, etc.) and implement stability and transport studies
Qualify and validate production and/or subcontracting processes and ensure training for employees involved in the transfer (production staff, quality control, subcontractors, etc.)
Monitoring, Continuous Improvement and Optimization: analyze manufacturing and QC processes and product performance to identify areas for improvement and implement optimization strategies
Participate in the resolution process, working with cross-functional teams to address and mitigate potential problems
Drive continuous improvement initiatives, focusing on enhancing product performance and extending product lifecycles
Ensure the traceability of the project and product documentation
Establish quality documentation (instructions, forms, supporting documents, etc.) related to the product/process/changes
Record the traceability of changes and/or transfer steps in the quality process using a quality tracking software
Participate in the development and implementation of supply and quality processes

Qualifications

Strong engineering background — Master’s degree / Engineer degree with solid experience (5-8 years minimum) in electrical, mechanical engineering within biotech, medtech, diagnostics, or microfluidics systems. Ideally, experience in transfer activities.
Advanced analytical expertise — Solid experience with analyzing data and identifying trends to optimize product performance.
Solid experience in Control design and definition — Knowledge in determination of CQA, AQL, residual risk (customer/supplier), control method capability (CMC), and process capability (Cp/Cpk).
Regulated environment expertise — Comfortable working in regulated environments (ISO 13485, GMP-like systems).
Project management experience — Leader, autonomous, organized, proactive in project management.
External communication — Ability to negotiate with several teams, suppliers or subcontractors and support quality audits.
Team spirit — Easy and clear communication, intellectual curiosity with sharing spirit.
Languages — Fluent in French; high-level English suitable for regular professional use.