For our client GSK, specialized in Consumer health products, localized in Nyon in Switzerland, we are looking for a :
QC Validation Scientist
1-year temporary mission
Your mission
Ensure the following of QC Validation project activities : Change Control, protocol/report, transfer In/Out. Manage project to ensure Timing, Quality.
Your responsibilities
- Provide expertise in all analytical equipment and method to help QC and production investigation
- Manage the investigation: Deviation, laboratory investigation (LAB) to facilitate solutions to complex challenges
- Utilize proactive thinking to generate creative solutions to complex technical problems
- Respect all GMP standards. GMP knowledge and experience to support the requirements expected by Swissmedic, European union agencies and other regulatory bodies to assure that our products meet all cGMP requirements together with our operations and documentation system
- Create SOP, protocol, report and working documentation for these activities
- Ensure the work in the respect of SSE rules
- Manage Change Control related to QC Validation activities
- Manage Transfer In/out : protocol/report, Timing, evaluation, impact, relationship
Your profile
- Bachelor or Master in Chemistry
- 10-year experience in pharmaceutical industry is preferred
- Previous experience in GMP
- Fluent in French, good level in English
Your application
Please apply on-line. For more information, contact Ms Sophie Darthenay
