Specialist, Manufacturing Automation Merck Sharp Dohme Msd

5.0 - 7.0 years

3 - 18 Lacs

Hyderabad, Telangana, India

On-site

Responsibilities: Develop and/or modify process models for Drug Substance, Drug Product and Packaging operations using discrete event simulation Provide technical support for process optimization analysis, such as debottlenecking, capacity analyses, and what if analysis for manufacturing operations Assist technical OOPT members with data analysis for manufacturing system integrations and the debugging/testing of data interfaces using SQL. Provide customer support for the RTMS platform. This includes troubleshooting, escalating, and resolving issues reported by the users at the different sites Use of agile tools (e.g. Jira, Confluence) and methodologies (e.g. sprints) to deliver defined product increments Delivery in accordance with defined scope/time/acceptance criteria Required Education and Experience: B.S. in Science/Engineering or equivalent technical field with 5-7 years of relevant experience. Demonstrated experience in mathematical modeling and at least one programming/scripting language (e.g. C/C++, Matlab, Python, R, C#, Java). Ability to communicate effectively with both technical and non-technical personnel to achieve the desired outcomes Excellent, proactive written communication, coupled with the ability to divide assigned tasks into smaller increments to leverage the timezone differences across the team. For example, the ability to receive written feedback on a task from a colleague/customer working overnight, and then work independently to address the feedback and reply in writing so that the colleague/customer can review the completed task when their work hours resume. Strong analytical problem-solving skills and ability to work independently within the role s defined responsibilities. For example, although these roles work in collaboration with other technical team members, success will require the ability to proactively and independently overcome obstacles. Successful candidates should be prepared to apply their full expertise to situations and take appropriate initiative to solve problems. Ability to work both independently and collaboratively with a globally dispersed team Practice in Agile Methodology and Continuous Improvement and with a Digital & Innovative mindset Expertise in authoring and executing technical documentation following industry standards and methodologies (SDLC, AGILE) Excellent communication and problem-solving skills with a sense of ownership, enthusiasm, and innovation Preferred Experience and Skills: Process Manufacturing expertise, preferably in the pharmaceutical industry Prior experience as an industrial engineer or simulation developer, for example with a design engineering and/or A&E firm using discrete event simulation in the pharma industry is strongly preferred; prior experience as an automation/controls developer in pharma or an adjacent process industry is an advantage Familiarity with manufacturing scheduling, discrete event simulation, finite state machines, and associated algorithms Experience using SQL to query and analyze datasets, including metrics/KPI calculation Knowledge of manufacturing systems such as PAS-X MES, Aveva PI, etc.

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Senior MES Analyst NNE

7.0 - 11.0 years

9 - 12 Lacs

Bengaluru

Work from Office

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

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