Beschreibung
Role: QA Representative
Location: Zug, Switzerland (Mezzovico for Synthes)
Job Type: Contract
Rate: Negotiable
Start Date: ASAP
Role Profile:
Consultant for remediation complaint and non-conformities report received by distributors.
Skills:
1) typical consultant profile and related consultancy experience in medical device regulated environment (FDA)
2) HIGH UNDERSTANDING AND KNOW-HOW OF FDA REGULATION, related capacity of understanding the difference between remediation minimal requirement and remediation expanded requirements
3) ability to work in autonomy in a production environment, independent in retrieving information
4) ability to deliver in accordance to timeframe target of single NCR remediation
5) consultant spirit : capacity of delivery facing limited data available cases
6) pragmatic spirit
7) hands-on experience on the topic
8) previous top management experience is not considered a plus, the profile must be capable of deliver and it is not required to coordinate resources or other consultants
9) Knowledge & experience on SAP
10) Good knowledge of Office package
11) Language skills: English mandatory, German and/or Italian would be a plus