Ingénieur Qualité Système - Pharma (H/F)
Build a career that matters.
At made., we have built a model that allows consultants to commit to demanding projects without sacrificing either their work-life balance or their professional trajectory.
We see engineering consulting as a true profession, practiced at the heart of our clients’ projects.
We support healthcare industrial players in their most critical quality projects, within demanding regulated environments: pharmaceutical, biotech, medical devices.
Above all, we have chosen to break down silos and unlock career paths by putting people back at the center of consulting.
Here, you work on projects that matter, within a socially committed framework, with a trajectory designed for the long term.
Your role
As part of a strategic project within a major pharmaceutical site, you will contribute to the evolution and strengthening of the quality management system in a demanding GMP environment.
En tant qu’Expert Qualité Système, vous jouez un rôle clé dans la structuration, la conformité et l’amélioration continue du QMS, en lien étroit avec les équipes qualité, production et support.
Votre expertise contribue à sécuriser la conformité réglementaire du site et à renforcer la performance du système qualité.
Your day-to-day
You will contribute in particular to:
the evaluation and continuous improvement of the site's quality management system.
the management and continuous improvement of quality documentation.
leading or supporting deviation management, CAPA implementation and change control activities.
the preparation and support for internal audits and regulatory inspections.
the harmonization and continuous improvement of quality processes.
supporting operational teams in the implementation of GMP requirements.
contributing to continuous improvement initiatives within the QMS.
Your profile
You have a scientific background (Pharmacist, Engineer or equivalent) and significant experience in quality systems within the pharmaceutical industry.
You have a strong knowledge of GMP standards and experience working in highly regulated environments.
You are recognized for:
your rigor and expertise in quality.
your ability to structure and enhance quality systems.
your ability to work effectively in cross-functional environments,
your ability to communicate with diverse stakeholders (Quality, Production, Engineering).
At made., commitment, curiosity and personal growth matter just as much as expertise.
Why join made.?
Joining made. means:
• practicing consulting as a true profession,
• working on structuring projects, not opportunistic assignments,
• growing through the diversity and complexity of client projects,
• being supported in your development through a simple, direct relationship,
• building a coherent and evolving professional trajectory.
Want to learn more?
We take the time to talk.
Send us your application in complete confidentiality.