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Senior OSi Aveva Pi Engineer

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Job Location drjobs

Indianapolis - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Job Description

Horizon Controls Group are seeking a highly skilled and experienced Lead AVEVA PI System SME (OSI PI) Engineer with a minimum of 7 years of experience in the pharmaceutical sector. The ideal candidate will possess deep expertise in the AVEVA PI System and its applications within the pharmaceutical industry.

Role: As the Lead AVEVA PI Engineer, you will play a critical role in designing, implementing, and maintaining the AVEVA PI infrastructure, data integration, and reporting solutions to support data-driven decision-making and operational excellence.

Responsibilities:

AVEVA PI Infrastructure Design and Implementation: Lead the design and implementation of the AVEVA PI (OSI PI infrastructure), including data collection, historian configuration, data modelling, and interfaces. Collaborate with cross-functional teams to ensure the infrastructure meets the specific needs and requirements of the pharmaceutical manufacturing environment.

Data Integration and Interface Development: Develop interfaces and integration solutions to collect data from various sources within the manufacturing environment, including process equipment, SCADA systems, and laboratory information systems (LIMS). Implement data mapping, cleansing, and transformation processes to ensure accurate and reliable data storage and retrieval in AVEVA PI.

System Configuration and Administration: Configure and administer the AVEVA PI System, including the creation and management of tags, data archives, and security settings. Monitor system performance, troubleshoot issues, and optimize system configurations to ensure high availability and data integrity.

Data Visualization and Reporting: Design and develop intuitive and insightful data visualization and reporting solutions using AVEVA PI (OSI PI) tools (e.g., PI Vision, PI ProcessBook). Collaborate with stakeholders to define key performance indicators (KPIs), develop dashboards, and generate reports to support data-driven decision-making and operational performance monitoring.

System Integration and Collaboration: Collaborate with IT, automation, and process engineering teams to integrate the AVEVA PI System with other manufacturing systems, such as MES, ERP, and quality management systems. Ensure seamless data exchange and interoperability between systems to enable comprehensive data analysis and reporting.

System Upgrades and Maintenance: Lead system upgrades and patches for the AVEVA PI infrastructure, ensuring minimal disruption to ongoing operations. Develop and implement preventive maintenance strategies to ensure the stability, reliability, and security of the system.

Project Management: Manage and oversee AVEVA PI implementation projects, including project scoping, planning, resource allocation, and coordination of activities. Monitor project timelines, budgets, and deliverables to ensure successful project execution.

Training and Knowledge Transfer: Provide training and knowledge transfer sessions to end-users and stakeholders on the AVEVA PI System, data visualization tools, and best practices. Promote user adoption and self-sufficiency in utilizing AVEVA PI (OSI)for data analysis and reporting.

Regulatory Compliance: Ensure that the AVEVA PI System and associated processes comply with regulatory requirements, such as FDA guidelines, data integrity, and GMP standards. Collaborate with quality and compliance teams to develop and enforce validation protocols, documentation practices, and change control processes.



Requirements

Bachelors degree in a relevant field (Engineering, Computer Science, or related discipline). Advanced degrees or certifications related to the AVEVA PI System (OSI PI system) are preferred.

Minimum of 7 years of experience working with the OSI PI system within the pharmaceutical sector.

Deep understanding of AVEVA PI -architecture, data modeling, and system configuration best practices.

Proficiency in developing interfaces and integrating OSI PI with various data sources and systems (e.g., SCADA, LIMS, MES, ERP).

Expertise in data visualization and reporting tools, such as PI Vision, PI ProcessBook, and Microsoft Power BI.

Strong project management skills, with the ability to lead and coordinate complex projects, manage timelines, and deliverables.

Excellent analytical and problem-solving abilities, with a keen eye for detail. Ability to analyse complex data sets, identify trends.



Providing independent quality review and approval of system lifecycle documentation, such as plans, requirements, risk assessments, protocols and reports for new and modified systems. Providing independent quality review and approval of system changes. Supporting and approving computerised systems investigations and test deviations. Ensuring consistent approach to qualification, change and deviation management across systems being implemented on the project. Providing timely and pro-active QA IT support and guidance to facilitate project timelines, including close collaboration with the technical and business units. Where required, engaging with QA IT teams from other sites and capital projects to standardise and align approach to computerised systems compliance. Experience: Min. 5 years of experience in QA IT/CSV, CSV and/or a similar role in the pharmaceutical industry. Working knowledge of relevant regulations and industry standards. Proven ability to meet timelines, prioritise tasks and engage with stakeholders. Excellent communication skills. Project management experience will be an advantage. DeltaV

Employment Type

Full Time

Company Industry

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