This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Looking to join a growing industrial company through an international development program? Interested in contributing to projects across several of our sites worldwide, building strong operational experience, developing your skills quickly, and following a personalized career pathway? Join Nemera’s NextGen Engineering Program ! In a context of strong international growth and the development of new projects across our various sites, Nemera is strengthening its commitment to training and supporting young engineers through its NextGen Engineering Program. This international permanent-contract program offers a structured pathway that enables participants to contribute to major Group projects while developing their skills in a stimulating technical environment. Participants will complete several successive assignments across different Nemera sites in order to gain solid, varied experience with strong exposure to industrial innovation. At the end of the program, they will join our teams on a long-term basis with a highly structured international pathway, dense and diversified operational experience, and reinforced mastery of our standards and project practices.
Job Responsibility:
Be integrated into project teams and participate in meetings as the primary point of contact for all quality-related aspects
Ensure project quality oversight by informing the Project Manager and the Project Quality Manager of progress and any events that may impact product quality
Identify quality control and monitoring requirements for new products based on specifications and customer expectations
Develop general and product-specific quality instructions for new products
Participate in or lead regulatory submission dossiers as needed
Train quality control, production, and quality support teams on the inspection of new products
Release the first production batches under the authority of the Project/Product Quality Manager
Transfer all quality-related information and instructions to the Operational Quality Manager
Build validation teams, manage validation files, and monitor the progress of equipment and process validation activities
Act as the quality contact for equipment suppliers subject to validation
Monitor product and process changes throughout the entire lifecycle
Conduct periodic reviews (monthly or annual) and analyze the results
Act as the quality interface for customers during industrialization and over the product’s entire lifecycle
Contribute to the success of customer, regulatory, supplier, and internal audits
Requirements:
Engineering degree in quality, industrial engineering, materials, biomedical engineering, or a related field
Knowledge of European and U.S. regulatory frameworks applicable to medical devices or other regulated environments
Good command of GMP and quality tools (FMEA, risk management, validation, etc.)
Strong communication skills and ability to work with varied stakeholders (internal teams, customers, suppliers, auditors)
Strong analytical mindset, rigor, organization, and reliability
Cross-functional leadership and ability to manage multiple topics simultaneously
Excellent level of English is essential
A strong appetite for international exposure is key, as it is at the heart of the program’s DNA
What we offer:
Permanent contract (CDI equivalent) from the start of the program
The program is structured around three successive assignments of approximately two years each, designed to progressively build technical, operational and leadership skills
First assignment on one of our sites (France / Germany / Poland / USA / Brazil), followed by assignments on other Group sites
Ongoing HR support and dedicated mentorship throughout the program
A structured career pathway offering rapid skill development and strong exposure to a wide range of industrial and strategic projects within the Group