description du poste
We are looking for a Validation Equipment Specialist to support our validation activities for production equipment of a pharmaceutical environment. The ideal candidate will have hands-on experience with equipment validation.
Your qualifications:
- Perform validation activities on production equipment such as reactors, autoclaves, water systems, filling lines, etc.
- Prepare, execute, and review validation documentation (URS, DQ, IQ, OQ, PQ) in compliance with GMP regulations.
- Use Kneat for authoring, reviewing, and managing validation deliverables in a fully digital format.
- Collaborate with cross-functional teams including engineering, production, QA, and maintenance.
- Participate in risk assessments and define validation strategies for new and existing equipment.
- Manage deviations, CAPAs, and change controls related to equipment validation.
- Contribute to continuous improvement initiatives within the validation framework.
Your profile:
- Scientific or engineering background (pharmacy, biotechnology, industrial engineering, or similar).
- Strong understanding of GMP guidelines and GAMP 5 principles.
- Proficient in using Kneat for validation lifecycle management (mandatory).
- Familiarity with equipment validation : process, cleaning, lab, ...
- Detail-oriented, well-organized, with strong communication and teamwork skills.
- Comfortable working in both French and English (written and spoken).
-You master Microsoft Office Suite (especially, Excel).
-You already have experience using SAP, Veeva, and/or Kneat.
-You have knowledge in reporting/data management tools.
What we offer you:
- A full time, permanent AKKODIS contract with an attractive salary package including a company car, insurances, meal vouchers, etc.
- A position where you can grow and develop your career
- A super nice work environment & atmosphere within an international group
- A nice work/life balance with hybrid working model (on site + remote)
Interested? Send your resume to me via: Roufaidaa.EL-AMERI@akkodis.com