Description
An exciting contract opportunity has arisen for experienced Validation Engineers (German speaking) focussed on process validation working for a Global Biologics company at one of their European manufacturing campus`s.As Process Validation Engineers you will be expected to be:
* Perform a variety of moderately complex tasks under direct guidance and in accordance with current GMP`s and Procedures.
* Hands on in the development and execution of Process Validation activities. Executes validation studies for cGMP-critical processes to demonstrate compliance to cGMP, User- and Regulatory requirements.
* Generates validation documentation (protocols/reports) and provides assistance with the execution of protocols.
* For validation activities for which appointed, responsible for the validation documentation through approval and implementation.
* Develops moderately routine protocols to ensure quality standards.
*Application of the policy on the welfare of the employees and the environment corresponding the attained education and instructions by i.e. the correct application of work equipment and personal protective equipment, the reporting of incidents and non-compliances and the assistance in the identification of risks and preventive measures
Skills experience required:
*Must be able to speak/ write in German and English
*Strong experience of Process
*Strong experience of writing Process protocols
*Must be experienced in witness testing
*Must have a background of working in similar role for biopharmaceutical or pharmaceutical organisation.
This is exciting opportunity for an experienced process Validation professional fluent in both English and German languages. Please apply now for more information.