Freelance Validation Specialist (Pharmaceutical) (69152328)

 ‐ Onsite
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Keywords

Writing Clean room

Description

In this position you will be responsible for the writing and execution of project and system qualifications, validations, re-qualifications and revalidation of manufacturing facilities, equipment, utilities and processes. Fifty percent of the work is done in an office environment or conference room. The other fifty percent of the work is performed on the shop floor (i.e. executing of protocols themselves, etc.). Some of this work requires entry into a laboratory or cleanroom setting.

Start date
ASAP
Duration
7 months
From
Morgan Green
Published at
08.06.2016
Contact person:
Peter Nieuwpoort
Project ID:
1144549
Contract type
Freelance
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