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Form of workJob Description
Job Description:
Qualifications:
PAY RATE: 94.80/HR
- Client is a diversified specialty biopharmaceutical company whose mission is to Client, develop and deliver innovative medicines that help patients prevail over serious diseases.
- Client is looking for consultant engineer responsible for development, maintenance and support of the global Manufacturing Execution Systems (MES) solution-Syncade that is utilized globally across the Digital Plant manufacturing network to produce medicine.
- This includes successful delivery of projects and continuous improvement initiatives focused on effectiveness and cost reductions in manufacturing operations.
- Syncade MES solution scope includes software(recipe) components, configuration, recipe and object libraries, interfaces, reports and any customizations that support the Digital Plant manufacturing operations
- Responsible for delivering simple to complex changes to application or recipe build within the MES solution-Syncade(emerson)
- Partner with business partners to understand business requirements and translate to MES solutions
- Responsible for assessing the risk and impact that changes, patches, outages or other events can have to the MES solution.
- Responsible for testing MES syncade recipes that interfaces to ERP (Enterprise resource planning), CMMS (Asset calibration system), Quality execution systems including LIMS, Process control systems (DeltaV,etc.) and other digital solutions.
- Ensuring compliance with data integrity and computer system validation requirements and regulations as a part of MES recipe Development and testing.
- Understand changes that impact validated state of application and underlying infrastructure.
Qualifications:
- 5+ years' work experience, with at least 5 years' experience in GMP execution systems
- Bachelor of Science in an Engineering or other Science discipline, Computer Science, or Management Information Systems.
- Specific experience in process automation, MES and batch manufacturing industry standards (ISA S88 &S95)
- Direct experience designing, building, deploying and supporting automation and execution systems (SCADA, MES, PAT, OSI Pi Data historian, etc.) in a regulated manufacturing environments in pharmaceutical or biotech industry.
- Strong domain expertise in the application of IT to manufacturing, including a broad understanding of processes and how they are supported by IT tools and systems.
- Strong knowledge of regulatory landscape and demonstrated experience with software validation.
PAY RATE: 94.80/HR
