Job Description:
The company is seeking a Manufacturing Engineer to maintain the MES environment, author and maintain recipes and worksheets, troubleshoot issues and provide solutions for MES and SAP problems in recipe execution and authoring.
This role requires strong knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry. The successful candidate will have experience of batch processing operations in an FDA/HPRA regulated industry.
The team member will be responsible for designing, creating, writing and executing test and validation protocols, risk assessments and system documentation. They will also participate in MES knowledge exchanges, MES Governance meetings and manage issues, work-arounds and fixes identified.