Validation Technical Specialist

Italy  ‐ Onsite
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Keywords

Description

Validation Technical Specialist - 12 Month Contract - Italy

A leading global pharmaceutical organisation requires a Validation / Technical Project Specialist to join their fill finish manufacturing facility based in Italy. The purpose of the position is to verify and update CMO (Contract Manufacturing Organisations) validation activities that has been completed.

The Role:
*Communicate daily with CMO`s (Contract Manufacturing Organisations)
*Review protocols
*Writing protocols
*Process validation
*Cleaning validation
*Hold time studies
*Filter validation

Experience:
*Degree educated in either Science or Engineering
*Biopharmaceutical or Pharmaceutical manufacturing experience is essential
*Sterile / Aseptic experience
*Hold time studies
*Process validation
*Cleaning validation
*Filter validation
*Process Development
*Technical Transfer experience
*Fluent in English although the ability to speak Italian will be highly advantageous

The position would suit a junior to mid level Validation Engineer/Technical Specialist with 2-5 years experience. An outstanding daily rate is on offer alongside an exceptional opportunity to join a leading pharmaceutical organisation based in Italy. Please apply today with a covering letter highlighting your key skills and relevant experience aligned to this contract opportunity.
Start date
n.a
From
Quanta Consultancy Services
Published at
17.09.2012
Contact person:
Lee Mitchell
Project ID:
421490
Contract type
Freelance
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