AS&T Specialist CGT
Novartis
- Suisse
- CDD
- Temps-plein
- Support analytical method transfer and validation activities
- Coordinate/support AS&T projects
- Support stability programs (e.g. protocol/report writing)
- Product and process validation support
- Implementation of new techniques/technologies and method optimization
- Ensure all activities in compliance with cGxP, incl. data integrity
- Comply with all HSE guidelines
- Detect and report potential accident, risks and propose solutions
- Participate in HSE risk assessments
- Preparation and participation to internal HSE audits
- Responsible for participating in initial training and retraining
- Sound technical understanding; experience in pharmaceutical or chemical analytics/QC (incl. equipment qualification) or equivalent
- Technical education & 3-5 years relevant experience or
- Desirable University degree in Pharmacy, Chemistry or equivalent + 0-4 years working experiences
- Good (oral and written) in English; fluent in local language (oral and written)
- Collaboration; result-oriented
- Breakthrough Analysis; Being Resilient; Operational Excellence; Statistical analyses; Continuous Learning
- MS Office applications and other standard IT applications supporting Quality activities
- Laboratory equipment; Quality Control (QC) Testing; Quality Control Sampling; Knowledge of TQM and related industry GxP standards and processes; Laboratory Excellence; Quality decision making; Good communication skills.