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Analytical methods validation specialist (réserve de recrutement)

Ypres
Akkodis
Publiée le 17 janvier
Description de l'offre

Analytical Methods Validation Specialist (Réserve de recrutement)


About us:


Akkodis is an organization with more than 1,000 engineering, scientific and digital experts in Belgium. Our mission is clear: create a smarter future together! We are a one-stop-shop for engineering, IT, Life Science, and new technologies. Our combined passion for talent and technology allows us to look at the world differently.


With our 360° offer we support companies in all sectors in implementing Smart Industry solutions, from the up and reskilling of entire teams to the delivery of complete projects. Our added value? We make incredible happen!


What responsibilities will you have?


As Analytical Methods Validation Specialist, you are in charge to:

* Participate to the reflection of the validation design and the treatment of experimental data in collaboration with different stakeholders (QC technicians, test supervisor, QC manager and/or QA specialist).
* Write validation documents (Validation protocols/reports, Qualification protocols/reports, Rational documents, Comparability documents, etc.).
* Participate to the investigation phases in case of acceptance criteria unmet,
* Participate to the management of quality element (CAPA, eCC, Deviation, etc.) in relation to validation projects.
* Participate to transversal interactions with other teams in QC Department and different other stakeholders.
* Participate to the administrative tasks of the team (complete follow-up files, continuous improvement, etc.).
* Guarantee the application and maintenance of adequate cGMP rules in his work area.


What skills do you bring to the table?


* You are graduated as a master’s degree in pharmaceutical, bioengineering or chemistry, with a good expertise in biochemistry, analytical chemistry, or other related science.
* You have a good expertise in some physico-chemical methods, like UPLC-MS, GC-MS, LC-MS, etc.
* You have good knowledge in validation of analytical methods and cGMP environment.
* You are fluent in French, and you have good knowledges in English (written and spoken).
* You have advanced written and verbal communication skills.
* You enjoy meeting and speaking with people, presenting results, and advising costumers.
* You are proactive, solution-oriented, open-Minded, organized, and flexible.


What’s the offer you can’t refuse?


As an AKKODIS Team member, you will be:

* Onboarded in your position via a buddy process
* Supported in your career by your Business Manager
* Actor of your training plan and your personal and professional development
* Benefiting from a permanent contract
* Benefiting from a competitive salary package including several extra-legal benefits


Do you any questions? You can contact me at marie.defruit@akkodis.com

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