MES Engineer
Position is 50% Onsite: Provide support for an integrated manufacturing execution platform. Part of a team to ensure reliable 24/7 operation of site and integrated systems. Develop methods for maintaining and documenting adherence to Client policies and procedures for manufacturing and information systems.
Principal Responsibilities:
- Design, develop, and implement the Manufacturing IT systems capabilities.
- Develop and maintain a MES support strategy that integrates process knowledge, equipment design, and quality standards with information technology to reduce down-time, elevate the level of regulatory compliance, and introduce efficiency gains through effective use of available technologies.
- Support of manufacturing and reporting systems that support the creation of electronic batch records and facilitate product release.
- Responsible for the software and data maintenance of computer systems used for the development, testing, and the production of our site and use of MES is CAR-T based only.
- Work closely within the Client organizations in the evaluation and implementation of MES application updates and changes.
- Support software and configuration required for external systems interfaces such as DeltaV, SAP, LIMS, and Oracle ERP.
Qualifications:
- Minimum of a Bachelor's degree in an Engineering field with at least 5 years of experience working in the pharmaceutical industry, preferably in the biotechnology sector.
- Knowledge and experience with MES technologies. Syncade and DeltaV would be preferable. Database technologies also a plus.
- Demonstrated leadership skills and experience working in diverse, multi-disciplined work groups.
- Experience and/or substantial understanding of process control principles and common system vendors' available products.
- Demonstrated expertise and competence in integrated recipe design in MES systems.
- Ability to work in a diverse work environment, manages multiple priorities, and at times, be self-directed.