Beschreibung
Ideal Background* Demonstrated leadership ability
* Excellent communication skills, to quickly build credibility within the Quality and Compliance community, executive management, external regulators, and industry - Both verbal and written
* Excellent presentation, facilitation and training skills
* Strong collaboration and influencing skills to partner effectively with other functions and across sites
* Team building and development capabilities
* System design and management skills - Organizational and Quality Systems
* Expert knowledge of the US Quality System Regulations and ISO 13485
* Demonstrated track record of delivering best in class results in the Quality Systems area
* Fluent in German and in English - able to interact, generate processes and procedures and educate and train
Strong knowledge of quality and compliance for Medical Device Industry (GMPs).
* Working knowledge of Quality System Regulations.
* A good working knowledge of related functions such as Operations, Supplier Management, Product Development and Procurement
* Experience in FDA QSR and ISO 9001/ISO 13485 standards, additionally a working knowledge of PAL and other related medical device national regulatory standards
* Demonstrated knowledge of business impact of compliance issues and risk management
* Proven ability to build partnerships both internally and externally
Language proficiencies:
-English and German spoken and written;
Place of work:
- Switzerland¨
- Office-based, 5-day/week
More Details:
- 12 Months fulltime
- Location: Central Switzerland
- 100% onsite
- Start date: Mai 2013
Please notice: European citizens are preferred
For a confidential discussion about regulatory affairs projects in Switzerland, or to apply, then send your CV to or call me.
I am a specialist recruitment consultant in regulatory affairs for the Pharmaceutical & Biotechnology industry. I offer a number of search options within the industry with a special focus on Switzerland.
If you are a Pharmaceutical professional looking for your next opportunity, then please don't hesitate to get in contact with me. Alternatively if you are currently looking for skilled individuals for the development of your organisation, then I can certainly help.
Your personal contact:
Kristina Bröckel
Regulatory Affairs Consultant
Tel:
mailto:
To find out more about Real please visit www.realstaffing.com