Beschreibung
Duties and responsibilities:- Writing and critical review of validation protocols,
- Review of Quality Control data and reports
- Performing CAPA and change control
- Ensuring all relevant Company and Agency policies and procedures are known and applied as required
- Deliver consistent high quality work
- Team and project management
Requirements:
- Bachelor or Master level in biology or related discipline
- At least 4 years of experience in QA , preferably in Pharmaceuticals
- Knowledge of Quality system regulations, guidelines, principles and practices
(GMP, CAPA, CSV, Quality Management)
- Very good communication skills & proactive personality
- Strong work ethic
- Languages: English, German, other languages (French, Italian) are a plus
Keywords:
QA, Quality consultant, Quality specialist, CSV, GMP, CAPA, Quality Assurance, quality, Pharmaceutical
English, German, Switzerland, freelance, temporary