Responsibilities :
- Analyse manufacturing processes and requirements to develop MES Model Requirement Specification.
- Model MES workflow according to the MES Model Requirement Specification.
- Conduct testing of MES workflow and lead user acceptance tests.
- Manage the deployment of MES workflow to the production environment.
- Drive MES continuous improvement to enhance ease of use, error-proofing, and integration with other enterprise systems (e.g., SAP, EAM, PLM, LMS, etc.).
- Collaborate with the Global MES Developer team on required system improvements.
- Provide support to end users as required to ensure manufacturing operation continuity.
- All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities.
Requirements :
Working experience in MES, with a preference for CAMSTAR MES.Candidates with more than 7 years of working experience will be considered for senior position.Previous exposure to a medical device manufacturing environment.Familiarity with ISO13485 and FDA CFR820.Project management experience.Strong problem-solving and data analysis skills.Team player with excellent interpersonal and communication skills.Independent and self-motivated.Education :
Degree in Information Systems, Computer Science, Engineering, or equivalent.Skills Required
System Integration, Sql Scripting, Data Modeling, Process Mapping, User Training