Essential Duties and Responsibilities:
- Architecting, implementing, and integrating solutions focused on tracking, analyzing, and improving the manufacturing process project(s) in a regulated environment.
- Designing and implementing data management strategies for the integration of MES solutions with JDE and plant automation equipment (DeltaV).
- Conceptualizing solutions during the design phase of the project life cycle
- Manufacturing execution system configuration, programming, debugging, and testing
- Creating documentation including project design traceability documentation, test cases, and more
- Leading and guiding cross functional teams from concept to deployment in MES projects of any size
- Customer facing interaction and technical communication skills.
- Mentoring colleagues on your expertise and knowledge base
Technology Requirements:
- ERP Platform: JDE
- MES Platform: Siemens Opcenter Execution Process (formerly known as SIMATIC IT Unified Architecture for Process Industries)
- Distributed Control System (DCS): DeltaV
- Database Platforms: Microsoft SQL, Oracle, etc.
- Project Documentation: Microsoft Office
Education and Skills Requirements:
- Experience in MES Implementation, preferably Siemens Opcenter
- Minimum 5 years working experience with some or all the listed “Technologies Used”, as mentioned above.
- Minimum 5 years working experience in Pharmaceutical/biotech industries.
- Experience in FDA regulated industry and familiarity with CFR 21 Part 11, cGMP
- Technical attitude: ability to learn new systems and information quickly.
- Demonstration of in-depth technical capabilities in system supported manufacturing in a regulated environment.
- Meticulous, conscientious, analytical, focused, self-starter individual.
- Excellent communication skills – both verbal and written