Inteldot · 1 day ago
MES Specialist (PAS-X)
Inteldot is seeking a MES Specialist (PAS-X) who will be responsible for the design, administration, and ongoing optimization of PAS-X systems in manufacturing environments. The ideal candidate will have experience with the PAS-X platform and will lead implementation and upgrade projects while ensuring compliance and operational excellence.
Information Technology & Services
Responsibilities
Analyze business and operational requirements to configure and design PAS-X solutions
Develop workflows, master batch records, and system specifications tailored to client needs
Ensure seamless integration of PAS-X with other systems, such as ERP, SCADA, and LIMS
Act as the System Owner for PAS-X implementations, ensuring operational excellence and compliance
Monitor system performance, resolve issues, and implement enhancements
Maintain comprehensive documentation, including system configurations and validation protocols
Oversee user management, role-based permissions, and data security within PAS-X
Coordinate software updates, patches, and system upgrades
Develop and implement protocols for system backups and disaster recovery
Lead PAS-X implementation and upgrade projects, ensuring adherence to scope, timeline, and budget
Collaborate with cross-functional teams, including IT, automation, and production
Manage vendor relationships and ensure the delivery of high-quality solutions
Conduct risk assessments and establish mitigation plans
Provide end-user training on PAS-X functionalities and workflows
Offer ongoing support and troubleshooting to ensure smooth system operation
Drive adoption of system best practices across the organization
Qualification
Required
Bachelor's degree in Engineering, Computer Science, or a related field
3+ years of hands-on experience with PAS-X MES platform
Proven track record of designing and managing MES solutions in GMP-regulated environments
Experience integrating PAS-X with ERP, SCADA, and LIMS systems
Proficient in PAS-X configuration, including master batch record development and system workflows
Strong understanding of GMP, FDA, and ISO regulations
Excellent problem-solving and troubleshooting skills
Exceptional communication and project management abilities