QA Validation Specialist

Vertragsart:
Vor Ort
Start:
2011-12-21
Dauer:
an initial 12 month contract
Von:
Quanta Consultancy Services
Ort:
DE
Eingestellt:
21.12.2011
Land:
flag_no Deutschland
Projekt-ID:
285330

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Leading Biopharmaceutical manufacturing plant currently has a contract requirement for an experienced QA Validation Specialist. Working on either their new Greenfield biotech manufacturing or their existing manufacturing campus in Germany.

Responsibilities to include:

. To document all validations according to current practices.
. To ensure that all documentation is prepared, authorised and completed in a timely manner.
. To ensure that validations are performed to current regulatory and industry standards.
. To ensure compliance to the section and site`s procedures.
. To liaise with various departments involved in the qualification and validation work to ensure efficient performance of the related tasks.
. Ensure cGMP is applied in their area of work and comply with cGMP in all areas of the business.

To be successful for this Quality Assurance Validation Specialist we require the following:-

. Degree Education
. Extensive experience within a Biopharma environment and associated equipment
. Experience working in large scale Greenfield or Brownfield biotech projects
. German speaking is ESSENTIAL

This is an exciting opening to work in dynamic team in long term contract opportunity. Please apply now for more information.