MES Analyst

NNE Inc.

Bengaluru

On-site

INR 900,000 - 1,400,000

Full time

14 days+

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Job summary

NNE is seeking an MES Analyst in Bangalore, India. The role designs, configures, tests, documents, and implements MES solutions for pharma manufacturing, ensuring compliant and efficient digital manufacturing aligned with regulatory expectations.

Candidates should have 3-5 years of MES experience, hands-on with PAS-X/Syncade/Opcenter, and knowledge of GMP, 21 CFR Part 11, data integrity. On-site five days a week with limited remote work is expected.

Qualifications

  • Bachelor's or Master's in engineering, CS, IT, Life Sciences
  • 3–5 years of MES experience in pharma or regulated environments
  • Hands-on experience with PAS-X, Syncade, or Opcenter
  • Strong GMP, GAMP5, data integrity, Annex 11, 21 CFR Part 11 knowledge
  • Ability to translate requirements into MES docs, workflows, and tests

Responsibilities

  • Execute MES design, configuration, testing, and implementation activities for work packages
  • Translate manufacturing requirements into MES workflows and configurations
  • Configure and support MES platforms for electronic batch management and production execution
  • Prepare design specifications, configuration records, test scripts, and validation deliverables
  • Conduct unit, integration, and user acceptance testing with traceability
  • Collaborate with Process, QA, Automation, IT, Production and Validation teams
  • Support troubleshooting, deviation handling, corrective actions, and deployment

Skills

Regulatory compliance
Requirements analysis
Stakeholder communication
Project coordination
Independent work
Multicultural collaboration

Education

Bachelor's or Master's in Engineering/CS/IT/Life Sciences

Tools

Körber PAS-X
Emerson Syncade
Siemens Opcenter

Job description

MES Analyst

We are a leading pharma engineering company shaping the future of API pharma engineering globally. Leveraging the expertise of 2,000+ employees across Denmark, India, and the US, we design, build and optimise pharmaceutical manufacturing facilities that are essential to the health and well-being of patients everywhere.

Our success is driven by passion, innovation, and collaboration — with our customers and across our teams and disciplines. If you share our dedication to a noble cause and our passion for API pharma engineering, then NNE is the place for you.

About the role

The MES Analyst contributes to the design, configuration, testing, documentation, and implementation of Manufacturing Execution System solutions for pharmaceutical and biotech manufacturing environments. The role delivers compliant, efficient, and reliable digital manufacturing solutions aligned with customer requirements and regulatory expectations.

Location

Bangalore, India

Experience

3-5 years

Department

Manufacturing Operations Management

How you might spend your days
  • Execute MES design, configuration, testing, documentation, and implementation activities for assigned work packages.
  • Translate manufacturing and business requirements into MES workflows, functional specifications, recipes, and configuration elements.
  • Configure and support MES platforms such as Körber PAS-X or equivalent solutions for electronic batch management and production execution.
  • Prepare and maintain design specifications, configuration records, test scripts, traceability information, and validation deliverables.
  • Execute unit, integration, and user acceptance testing; document evidence and support defect resolution and retesting.
  • Participate in requirement workshops, design reviews, customer discussions, and project coordination meetings.
  • Collaborate with Process, QA, Automation, IT, Production, and Validation teams to ensure compliant and practical solution delivery.
  • Apply GMP, GAMP5, data integrity, Annex 11, and 21 CFR Part 11 expectations throughout MES activities.
  • Support troubleshooting, deviation handling, corrective actions, system deployment, and continuous improvement.
  • Manage assigned priorities, communicate progress, and escalated risks, dependencies, or technical issues appropriately.
  • Contribute to reusable templates, lessons learned, knowledge sharing, and team best practices.
Who you are
  • Thrive in a collaborative and multicultural project environment.
  • Work in a structured, detail-oriented, and quality-focused manner.
  • Take ownership of assigned activities and follow through on commitments.
  • Communicate clearly with technical and non-technical stakeholders.
  • Are curious, adaptable, and motivated to strengthen your MES and pharmaceutical manufacturing knowledge.
  • Proactively identify questions, risks, and improvement opportunities.
  • Value feedback and contribute positively to team learning and development.
  • Are customer-focused, dependable, and solution-oriented.
What you bring to the role
  • Bachelor's or master's degree in engineering, Computer Science, Information Technology, Life Sciences, or a related discipline.
  • Minimum 3 to 5 years of experience in Manufacturing Execution Systems, preferably within pharmaceutical, biotech, or regulated manufacturing environments.
  • Hands-on experience with an MES platform such as Körber PAS-X, Emerson Syncade, Siemens Opcenter, or an equivalent solution.
  • Good understanding of pharmaceutical manufacturing processes, electronic batch records, recipes, workflows, and production execution.
  • Practical experience in MES configuration, documentation, testing, implementation, and validation support activities.
  • Working knowledge of GMP, GAMP5, data integrity, Annex 11, 21 CFR Part 11, and computerized system validation principles.
  • Ability to analyze requirements and translate them into MES documentation, workflows, configurations, and test cases.
  • Experience collaborating with Process, QA, Automation, IT, Production, and Validation stakeholders.
  • Good analytical, troubleshooting, communication, and coordination skills.
  • Ability to work independently on assigned work packages while contributing effectively to the wider project team.
Life at NNE.

NNE is short for Novo Nordisk Engineering. And for all of us who work here, NNE means so much more. At NNE, you become part of a vibrant, project-based environment built on close day-to-day collaboration. The role is therefore primarily on-site, with physical presence at the workplace expected five days a week. Limited flexibility for occasional remote work may be accommodated in line with business needs.

We are, at our core, a people business and, as such, committed to continuously developing our people and the way we work together. We do not expect you to know it all from day one, and we truly believe a great start makes a real difference. We therefore welcome new colleagues with our award-nominated onboarding programme, supported by a range of in-house talent and development initiatives designed to support your long-term growth.

Deadline of application is September 30, 2026

At NNE, we are committed to an inclusive recruitment process and equal opportunities for all job applicants. To maintain fairness, we request that you refrain from including a personal photo in your CV.

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