QC QA Validation Coordinator

One of our clients, a multinational company in the pharmaceutical industry currently requires a QA QC Validation Coordinator for Analytical Methods Validation

Start: 4/11/13
Length: 12 months
Location: Wavre

KEY RESPONSIBILITIES:

* Produce analytical methods validation documents for Biochemical methods:
- Establish strategy for methods to validate in collaboration with supervisor in charge of the method
- Translate strategy into validation protocol and experimental plan andcommunicate with supervisor and lab technicians in charge of the method
- Follow-up of experiments related to validations with laboratories and collect data
- Redaction of validation reports and submission to Validation Manager and QA

PREREQUISITES:

Education:

* Scientific degree

Knowledge:

- Fluent in French/English, written compentencies in English
- Good communication skills
- Ability to work under pressure due to the requested flexibility and reactivity of the activities
- Autonomous
- Hands-on mentality
- Ability to work in project teams in a multidisciplinary environmentand a matricial organization

Experience:

- Min 4 years' experience in pharma & with GMPs
- Experience in biochemical techniques (ELISA, MSD-HPLC, gel electrophoresis) is required.
- Confirmed experience in analytical method validation is highly recommended

Tags: Validation, QA, QC, Analytical Methods, chemistry, Pharmaceutical, Pharmaceutique, GMP