Validation Specialist (Chromatography Columns)

South East  ‐ Onsite
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Keywords

Description

A biotech manufacturing facility in the South East of England requires a Validation Engineer to focus on chromatography columns. The work will be to review, write and execute documentation.

Key Responsibilities:

* Protocol writing (including IQ, OQ, PQ and also have hands on experience of executing the validation), documentation reviews.
* Good planning, organisational and time management skills along with an ability to make decisions, solve problems, negotiate, influence and communicate with others is required.

You must have the following:

* Knowledge and experience working in a GMP environment.
* Biotech manufacturing experience.
* Knowledge and experience with Chromatography Columns.
* Be able to demonstrated excellent oral and written communication skills,and must be able to work in both a team environment as well as independently.

This is an exciting position for an individual who is ready to step up and deliver exciting projects on time and on schedule within a highly regulated industry. Please apply now for more information.
Start date
n.a
From
Quanta Consultancy Services
Published at
04.12.2012
Contact person:
Lee Mitchell
Project ID:
457020
Contract type
Freelance
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