Associate MES Engineer

MES Analyst

Who we are

We are a leading pharma engineering company shaping the future of API pharma engineering globally. Leveraging the expertise of 2000 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
DepartmentManufacturing 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 escalate 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 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:

Bachelors or Masters 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 youre ready to join our passion lets hear from you.

Deadline of application is September 30 2026

Questions before applying Please contact

Please note:
We only accept applications submitted through our online recruitment system
You do not need to attach a cover letter but please include a few sentences about why you are applying in your resume or CV
We invite to interviews on a running basis.

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.

Still searching for the right opportunity

If this position isnt quite what youre looking for but you know someone who would excel in this role please share this job post. And dont forget to explore our other exciting opportunities your future role at NNE might be just around the corner! Visit our Career Site

Required Experience:

IC