We are seeking a skilled Cleaning Validation Specialist to join our team. As a key member of the production department, you will be responsible for designing and authoring qualification/validation documentation and cycle development studies.
* You will execute execution/development of change controls, resolving technical issues encountered during study execution.
* Your primary duties will include engaging with production, maintenance, and quality representatives in assigned areas of operations.
* You will perform root cause analysis of system failures using standard tools and methods.
* Serving as validation representative for cross-functional projects, you will represent the validation team at global technical forums.
Qualifications:
The ideal candidate will have experience in cleaning validation including CD & PQ of mobile vessels and parts washers, recipe development & optimisation.
* You should possess relevant technical qualifications in Applied Pharmaceutical / Biological / Chemical sciences or applied Technical / Engineering qualification.
* You will have expertise in Exception / Deviation Management and Change Control, equipment and process validation.
The successful candidate will have a proven track record in delivering excellence, operating in a GMP manufacturing setting.