Qualified Person 2001/83 / EU (m / w)
Posted By: Merck Group
Call: 49 (0) 6151 72-
Number of Vacancies
Not Disclosed
Career Level
Experienced (Non-Managerial)
Skill/Keywords
Comprehensive knowledge in GMP / quality assurance Long-term experience in pharmaceutical production, quality control / assurance and / or development Knowledge of regulatory requirements in the field of drug licensing
Job Description
As a Qualified Person, you ensure that Merck KGaA medicinal products are manufactured according to the requirements of the German Medicinal Products Act (AMG) as well as the EC GMP Guideline or other regulations and checked for the required quality or compliance Are released. In addition, you are involved in the development, development, mediation and updating of quality standards. They pursue, analyze and interpret national / international legal requirements and guidelines and assess the compliance of processes and documents in your area of ??responsibility. You are a team member in local or global projects.
Extra Information/Requirements
English fluent with confident mastery of the subject vocabulary
Teamwork, customer orientation, outcome orientation