3 Emerson Syncade Jobs

The Manufacturing Execution Systems (MES) Consultant position is a full-time role dedicated to offering consulting services to clients within the biotech and pharmaceutical industries. As an MES consultant, you will collaborate with project teams to support MES implementation and maintenance. Your responsibilities will span across different phases of the software development life cycle, encompassing tasks like creating design specifications, recipe authoring, configuration, programming/scripting, project management, software validation, and unit testing. Effective communication and collaboration with both internal team members and external stakeholders are crucial aspects of this role. To excel in this position, you should possess a robust background in computer programming and be well-versed in MES software packages like Honeywell POMS/POMSnet, Werum PAS-X, Rockwell ProPack Data, Camstar, SAP ME, or Emerson Syncade. A minimum of 4-5 years of relevant work experience is required. Familiarity with the software development life cycle, including gathering user requirements, software code development, and test protocol execution, is essential. Proficiency in SQL queries and database concepts is a must, while knowledge of C#, VB, VB.Net languages is desirable but not mandatory. The role may involve travel to client sites within India and overseas, as necessary, and a willingness to embrace career development and feedback for future job growth is expected. Qualifications for this position include a Bachelor's degree in Science, Pharma Operations, Computer Science, Engineering, or Business Administration (BSc/MSc/BPharm/MPharm/BCA/BCS/MCA/BE/BTech/BBA/MBA). This position is based in Pune, India, with travel requirements of up to 100% based on client location.,

Why should you join MES team: We are looking for a Senior MES Engineer to join our hybrid team that bridges Process Automation and Manufacturing IT. This team plays a crucial role in delivering digital factory solutions by translating complex process requirements into optimized control strategies and master batch records (MBRs) using advanced MES and DCS platforms. You will work in an innovative, multi-disciplinary team of engineers and consultants focused on designing, developing, implementing and validating automation and MES solutions for the pharmaceutical and biotech industries. Your work will support clients in achieving compliant, efficient, and future-ready manufacturing operations. Location : Bangalore, India Seniority: 7-11 years Department: Manufacturing Operations Management How you might spend your days (Main Roles & Responsibilities) Leading or supporting the design and implementation of Master Batch Records (MBRs) for Clean-in-Place (CIP) and product manufacturing process using ABB 800xA batch management and PAS-X MES. Designing, developing, and optimizing Distributed Control Systems (DCS) and automation strategies using ABB 800xA or similar platforms. Facilitating requirement gathering sessions with clients to design workflows aligned with business processes and regulatory standards. Integrating MES (PAS-X) and DCS (800xA) systems to enable seamless batch execution, data integrity and traceability. Collaborating closely with cross-functional teams including process experts, validation engineers, and data historians (e.g., AVEVA PI System). Supporting system commissioning, testing and qualification activities in compliance with cGMP standards. Who you are: At NNE, we care about who you are as a person. In the end, how you work, and your energy is what impacts the effort we do as a team. As a person, you: Thrives in a collaborative environment and is a strong communicator. Is comfortable with customer relations and navigating project complexity. Is proactive, curious, and eager to innovate and learn. Appreciates feedback and uses it as a tool for personal and professional growth. The miles youve walked In all positions there are some things that are needed, and others a bonus. We believe these qualifications are needed for you to do well in this role: B.E/B.TECH or M.E/M.TECH in Electrical Engineering, Chemical Engineering, Computer Science, or a related life science/engineering field. 2+ years of experience with MES platforms such as Krber PAS-X, Emerson Syncade, or any other proficient MES software. 2+ years of experience in DCS platforms, particularly ABB System 800xA or DeltaV or similar. Solid understanding of cGMP, ISA-88 batch control standards, and regulatory requirements for pharmaceutical production. Demonstrated experience with development, testing, and validation of manufacturing systems in a GxP-regulated environment. Experience in consulting or project execution is a plus. Were experts bound by a noble cause and driven by passion Sounds like something youd like to do? If youre ready to join our passion, lets hear from you. Deadline of application is 30 June 2025

Role & Responsibilities : For MES software Developer/tester experience requirement below as; Should have expertise/knowledge trouble shooting and installation on SQL Server or Oracle or MySQL Will have to work on store procedure, functions and join query, SQL job, transaction management in DB. Should have good exposure in manufacturing execution system (MES) on Syncade, Factory Talk and PAS-X Should have awareness Knowledge Oops concept. Should develop Windows form web application. Should work on MVC, .Net Core/VB script. Should work on Web API or WCF service or web service. Should have expertise JQuery and Javascript. Should have hands on experience in Crystal Reports of SSRS report. Should have knowledge of CSS and HTMLShould have experience on trouble shooting and software installation, integration third party software. Should have exposure documentation and good practices and Good communication skills. Qualification: B.E. Experience: 1 to 10 Years Preferred candidate profile: Candidates having experience in Pharmaceutical Industry will have an add on advantage.