Description
A Leading Biopharmaceutical manufacturing client has a contract requirement for an experienced Validation Specialist with QC Laboratory equipment experience.Working within the QC Function we are looking for a Validation Engineer to manage the validation activities of testing and laboratory equipment, carrying out the writing of the IQ/ OQ/ PQ protocols plus execution and completion of final validation reports. This will involve ensuring compliance is adhered to in respect of validation activities on matters of procedural documentation, change control quality systems & equipment verification.
To be successful for this role we are looking for the following skills & experience:-
* Strong cGMP background within either a Biopharma or Pharmaceutical environment
* Strong background in equipment validation including thermal equipment and laboratory equipment
* Experience within a 21CFR part 11
* QC Testing experience
* Experience in sterile manufacturing & testing
Laboratory equipment validation essential - HPLC GC Plate readers, laboratory instrumentation
PLease call for further details.