Description
Validation Specialist (Autoclaves)Duration: 6 months initial contract
Start Date: December 2014
Location: near Düsseldorf, Germany
Our biotech client is currently undergoing an extensive expansion and growth phase. It requires extra resource in its validation department to support ongoing project work. The successful candidate will be taking an active hands-on approach to execution of validation risk assessment and project activities.
Activity list:
• Responsible for the co-ordination of the validation activities for autoclaves and sterilisation equipment, temperature mapping and shipping.
• Review and approve protocols for IQ/OQ/PQ
• Risk assessments including QNAs
• Supporting other validation activities for biotech equipment as per project needs.
To be successful for this role you will have the following skills/experience :-
• Experience in the life science industry essential, biotech experience beneficial.
• Excellent knowledge of GMP/FDA requirements essential.
• Strong experience of supporting CAPEX projects required.
• Knowledge and experience of temperature mapping, autoclaves and sterilisation validation required.
• Experience of shipping validation and validation of other biotech equipment advantageous.