MES Engineer

Posted 11 Days Ago
Be an Early Applicant
Hiring Remotely in Pune, Mahārāshtra
Remote
Senior level
Consulting • Automation
The Role
The MES Engineer will gather user requirements, document and validate MES configurations, and provide engineering support for manufacturing execution systems. Responsibilities include evaluating biopharmaceutical processes, supporting site deployments, and improving operation procedures while adhering to safety and compliance standards.
Summary Generated by Built In

Company Description

JSat Automation is a global, full service, operational Consulting, Systems Integration & Validation firm headquartered in Blue Bell, PA. JSat Automation provides its client base with innovative and progressive operational consulting, engineering, data integration, and information technology solutions. JSat Automation utilizes domain specific process and technical knowledge, offers flexibility, leverages innovative business concepts and guarantees economies of scale to its clients through solutions that will save money in development time, startup costs and total cost of ownership. We are a fully integrated industrial automation, validation and information technology professional services business having global presence in the US, UK and Asia Pacific. JSat Automation serves customers in Pharmaceutical, Life Sciences & Biotechnology, Food & Beverage, Oil & Gas, Discrete manufacturing, and Energy industries.

Job Description

  • Gather user requirements and map existing manufacturing process to the MES, ERP and Process Automation systems.
  • Documentation and Validation of MES configuration and EBRs.
  • Evaluate biopharmaceutical processes develop/configure Electronic Batch Records (EBR)
  • Provide engineering and technical support for manufacturing execution systems and digital systems in the Biopharmaceutical Operations facility.
  • Evaluate and develop technology, plan, and implement modifications, troubleshoot and support manufacturing execution systems and other digital solutions.
  • Support site deployments of Emerson Syncade (MES). Examples of other relevant systems are Emerson DeltaV (DCS), Laboratory Information Management System, Asset & Calibration System, etc.
  • Adhere to, develop, and continuously improve the operation and maintenance procedures for process controls and manufacturing execution systems.
  • Work in a way that models respect for safety and EHS, quality compliance, data integrity, and engineering standards

Qualifications

  • Proven experience as a Senior Automation Engineer with increased levels of responsibility.
  • 5+ years’ experience designing, implementing, and supporting manufacturing automation solutions.
  • Pharmaceutical and/or Biotechnology industry experience desired.
  • Leadership abilities works well in a team environment

Additional Information

  • 3+ years’ Emerson DeltaV Batch experience required.
  • 3+ years’ MES (Syncade) experience in Life Sciences/Pharma.
  • Hands-on experience with Distributed Control Systems such as Emerson Delta V is preferred. Thorough understanding of ISA S88 and S95 models
  • MES recipe authoring, MES script writing, development, documentation, testing and implementation within a life sciences (biopharmaceutical) environment.

Top Skills

Emerson Deltav
Emerson Syncade
Erp
Mes
Process Automation
The Company
Blue Bell, Pennsylvania
83 Employees
On-site Workplace

What We Do

JSat Automation Inc. is a process controls, automation & MES systems and validation consulting & integration firm serving clients in industries including pharmaceutical, biotech, oil, gas, and chemical manufacturing. JSat Automation's edge has largely been due to a broad-base expertise in services and solutions ranging from feasibility studies to implementation. Projects and Services we provide include control strategy feasibility studies, system life-cycle documentation, design, configuration, startup support, and maintenance for clients in manufacturing industries. JSat Automation also provides validation services to the pharmaceutical industry with a particular emphasis on S-88 based system validation and 21 CFR 11.

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