Process Validation Specialist

Solothurn  ‐ Vor Ort
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Schlagworte

Beschreibung

To provide support for the validation activities associated with equipment, reagents, facilities, cleaning, test methods, and environment ensuring that all compliance issues and requirements of Validation Policies and Procedures are addressed. As a part of the global remediation quality plan (GRQP) to support the plant specific activities with investigations and remediation

Primary Tasks and Responsibilities:

Managing Complexity/Technical Accountability ? Serves as technical expert for the Validation process and responsibilities to ensure compliance ? Continuous Learning/Managing Risk ? Resolves & manages technical operational problems in area of expertise ? Suggest and sometimes may implement innovation and continuous improvement within the Validation process ? Implements initiatives in the Validation Process that will deliver customer value at lowest cost. ? Facilitates successful team behavior within Quality Systems and across functional areas ?

Requirements:

Experience in Process Validation, Mechanical and Chemical Processes
21 FDA 820
ISO 13485
Good documentation practice
German - good understanding / English fluent

If you feel suitable for this position you are very welcome to send me your online application.

To find out more about Real please visit www.realstaffing.com
Start
05/2013
Dauer
7 Months
Von
Real Staffing
Eingestellt
14.05.2013
Projekt-ID:
535621
Vertragsart
Freiberuflich
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