LIFE SCIENCES VALIDATION ENGINEER

Job description

Altran ranks as the undisputed global leader in Engineering and R&D services (ER&D), following its acquisition of Aricent. The company offers clients an unmatched value proposition to address their transformation and innovation needs. Altran works alongside its clients, from initial concept through industrialization, to invent the products and services of tomorrow. For over 30 years, the company has provided expertise in aerospace, automotive, defense, energy, finance, life sciences, railway and telecommunications. The Aricent acquisition extends this leadership to semiconductors, digital experience and design innovation. Combined, Altran and Aricent generated revenues of €2.9 billion in 2017, with some 45,000 employees in more than 30 countries.
As Validation Engineer:
- You will help define and support the Validation Approach,
- You will establish procedures for Validation in accordance with international standards (FDA, EMA, ICH, ASTM E2500, GAMP),
- You will write Validation documents (protocols, reports, SOPs, Critical Impact Assessments, …)
- You will manage deviations,
- You will coordinate and execute validation (IQ, OQ, PQ) tests,
- You will perform risk assessments,
- You will work in close collaboration with production, engineering, maintenance, QC, QA…
- You will ensure handover with final users.
Your profile
- Master degree in engineering or related scientific domains,
- Native level of French or Dutch and fluent in English,
- Relevant experience in Validation in a GMP environment is definite advantage
- Knowledge of management (project/team management)
Our offer
We’re not just offering you a job; we’re inviting you to be part of our community. We will provide you trainings, tools and grounds to work for top notch companies and engineer the career you like.