Job Description
As an Associate Manufacturing MES Specialist, you will be responsible for leading the deployment and support of various manufacturing systems.
Key Responsibilities:
* Reviewing and approving sessions of MES project deliverables against the overall project plan.
* MES Design Spec reviewing using the MR/BS and completed design spec/process flow map templates.
* Populating and completing review of MES documentation such as Config Spec (MESCS) and Trace Matrices (TMs).
* Leading Pre-PE executions (Static and Dynamic) and testing of MES records.
* Coordinating team on plant testing (Shakedowns) of MES documents with MFG SME.
* Coordinating team and documentation of all testing protocol and ensure GDP and compliance.
* Coordinating of Workflows for documentation approval.
* Reviewing of data for build of OPM recipes to support the MES build.
* Coordinating of MES Deployment Support - documentation readiness and change control support.
* Coordinating with area owners to ensure Process Area readiness for MES Deployment (hardware, barcoding etc.).
* Coordinating of sustaining deployed MES records to ensure timely close-out of executed MES records.
* Leading MFG element of launch activities in the lead up to MES records live on the production floor.
* Leading coordination of hypercare activities as part of wider MES team live on the production floor.
Requirements:
* Demonstrate knowledge and experience of MES preferably Werum PAS/X.
* Possess logical troubleshooting and problem-solving skills.
* Have excellent analytical, written and oral communication skills.
* Demonstrate an ability to work within a successful team.
Education and Experience:
You should have a BS/BA/BEng in a technical discipline, with 0-2 years of experience working within a Life Sciences manufacturing environment or equivalent combination of education and experience.