Duration: 12 months / possible extension
Home office: 20%
Workload: 100%
Responsibilities:
* Review and release of documents such as: analytical methods, method validations, specifications, risk assessments, deviation reports and investigations, change control records, stability reports.
* Preparation of product-related quality agreements
* Support of the supervised departments with GMP-relevant issues
* Carrying out self-inspections
Requirements:
* Degree in natural sciences
* Fluent written and spoken German and English skills
* At least 5 years of experience in the pharmaceutical industry
* Ideally professional experience in the field of pharmaceutical development (synthetic molecules, quality control or quality assurance)
* Knowledge of cGMP and quality requirements, ideally for clinical development phases
* Good IT skills (MS Office) - especially the handling of SAP, as well as other quality management systems (e.g. Veeva)
#J-18808-Ljbffr