Job ID: 37791134
Main Facts: Join the 220 employees of our Life Sciences & Chemicals division (ISO Certified)
Located in Woluwe-Saint-Pierre.
Technical skill 1: Validation procedures
Required level: 2/3
Technical skill 2: Validation documents
Technical skill 3: manage deviations
Required level: 3/3
Technical skill 4: validation IQ, OQ, PQ tests
Technical skill 5: know-how of standards FDA, EMA, ICH, ASTM E2500, GAMP
Soft skill 1: Innovation oriented
Soft skill 2: solutions oriented
Our company is a leader in innovation and high-tech engineering consulting. There are many programs to make your career thrive and grow here and abroad, and be coached by senior experts.
Keep learning was well with our Academy, seminars and Benchmark Expertise Project (BEP) sessions. And don’t forget to have fun: we are building a strong community of consultants thanks to internal social events!
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.