MES Analyst

NNE; Bengaluru; On-site; INR 1,200,000 - 1,600,000; Full time

Job summary

NNE is seeking a MES Analyst to design, configure, test, and implement MES solutions for pharmaceutical manufacturing. You will work with Process, QA, Production, Automation, IT/OT, and Validation to translate requirements into MES deliverables and ensure compliance with regulatory expectations.

The role emphasizes on-site collaboration in Bangalore, with exposure to GMP/GAMP5 and 21 CFR Part 11 guidelines, and a focus on durable digital manufacturing improvements.

Qualifications

• 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.

Responsibilities

• 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 elevate risks, dependencies, or technical issues appropriately.
• Contribute to reusable templates, lessons learned, knowledge sharing, and team best practices.

Skills

MES platform

PAS-X

Syncade

Opcenter

GMP compliance

GAMP5

Data integrity

21 CFR Part 11

Validation

Documentation

Stakeholder comms

Project coordination

Education

Bachelor or Master in Eng

Experience in regulated manufacturing

Tools

Körber PAS-X

Emerson Syncade

Siemens Opcenter

Job description

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.

You will collaborate with Process, QA, Production, Automation, IT/OT, and Validation stakeholders to translate manufacturing requirements into structured MES deliverables. The role requires practical capability in MES platforms, electronic batch records, testing, validation, and ownership of defined work packages.

Location: Bangalore, India

Experience: 3-5 years

Department Manufacturing Operations Management

How You Might Spend Your Days

As a MES Analyst, you will:

• 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 elevate risks, dependencies, or technical issues appropriately.
• Contribute to reusable templates, lessons learned, knowledge sharing, and team best practices.

Who You Are

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:

• 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

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:

• 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.

Did we spark your curiosity? If you’re ready to join our passion, let’s hear from you.

Deadline of application is September 30, 2026

Fair hiring:

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.