Qualification / Validation Engineer (M/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

Integrated as a consultant within our clients’ project teams, you work on equipment, facility, and/or process qualification projects in compliance with GxP / GMP requirements.
You are involved both in upstream analysis and hands-on execution, working closely with project, production, quality, and validation teams.
You are not on your own: exchanges are regular, straightforward, and focused on both your projects and your professional development.

Your day-to-day

Depending on the context and challenges, you may notably contribute to:

• defining qualification strategies,
• drafting and executing IQ / OQ / PQ protocols and reports,
• performing or leading on-site testing activities,
• identifying, analyzing, and addressing deviations and non-conformities,
• coordinating with project, production, quality, and validation teams,
• ensuring documentation traceability and regulatory compliance.

Projects are selected for their technical level, their alignment with your background, and their potential for skills development.

Your profile

You come from an engineering background or equivalent (industrial engineering, process engineering, quality, mechanics, chemistry, etc.) and have at least 3 to 5 years of experience in qualification / validation within a pharmaceutical, biotech, or medical device environment.
Senior profiles are welcome.
You have a strong command of GxP / GMP requirements and are comfortable working in demanding technical environments where documentary rigor and operational precision are essential.
Beyond technical skills, we place particular importance on rigor, analytical thinking, autonomy, and a strong sense of teamwork.
At made., commitment, curiosity, and continuous development matter as much as expertise.
We believe in careers built for the long term.

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.