We have a current opportunity for a Sr. CSV Consultant on a contract basis for 9 months with our International Medical device client. The position will be based in Switzerland mostly in-home office. For further information about this position please apply.
Responsibilities:
- Perform and lead several CSV Validations
- Implement EU-GMP Quality management system
- Update QMS towards ISO 9001 and desirable ISO 13485
Requirements:
- 8 - 10 years of CSV experience within Pharmaceuticals and Medical devices
- A problem-solving mindset: anticipating issues early
- Desirable project management skills
- Good working experience in agile methods
- Previous experience with implementation of EU-GMP QMS
Please note that due to legal restrictions, we can only accept people with Swiss or EU/EFTA citizenship or with an existing and valid residence and work permit for Switzerland/EU.
