- Get involved in different Quality and Compliance projects - Support the client during Internal and External Audits and inspections - Analyze current QA Processes in GxP Operations, define Performance Metrics and drive continuous improvements - Provide guidance with regards to compliance with Quality Policies and Procedures - Review records, SOPs, investigate deviations or non-conformities - Validate technical documentation - Perform Gap Assessments, Risk Assessments and Root Cause Analyses and help execute Corrective and Preventive Actions - Strengthen QA maturity & mindset through better Change Management, communication, documentation and training practices - Coach and train your peers on a specific subject matter - Be involved in the design and management of clinical studies - Participate in key projects such as product launches, divestment or integrations
Qualifikationen
- A graduate degree in Industrial Engineering or Bioengineering, Pharmacy, Chemistry or a related discipline in Life Sciences
- Knowledge of manufacturing standards in the Pharmaceutical Industry (e.g. GMPs)
- Project management experience or certification is a plus
- Fluent in spoken and written German and English
- Good communication and leadership skills
- Able to work autonomously and anticipate difficulties and risks
Wie bewerben?
Apply by sending your CV to Lucas Zaehringer at germany@avertim.de
Firma
Avertim Deutschland GmbH
Friedrich-Ebert-Anlage 36
60325 Frankfurt
Kontakt
Lucas Zaehringer
+49 69-24433-3116
germany@avertim.de