IT Specialists

NNE Inc.

Bengaluru

On-site

INR 4,000,000 - 6,000,000

Full time

14 days+

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Job summary

NNE is a leading pharma engineering company delivering MES solutions for global manufacturing operations. The MES IT Specialist will lead design, validation, and continuous improvement of MES in regulated environments, working with Process Engineers, QA, Production, Automation and IT/OT teams.

This on-site role in Bangalore requires deep MES expertise (PAS-X), ISA-88/95, 21 CFR Part 11, data integrity, and governance skills, with a focus on scalable, compliant digital manufacturing solutions and

Qualifications

  • Bachelor's or Master's degree in Engineering, Computer Science, Life Sciences, Information Technology, or a related discipline.
  • 12+ years of experience in MES within the pharmaceutical, biotech, or regulated manufacturing industry.
  • Strong hands-on experience with MES platforms such as Körber PAS‑X or equivalent MES solutions.
  • Deep understanding of pharmaceutical manufacturing processes and electronic batch record (EBR) solutions.
  • Expert knowledge of ISA‑88, ISA‑95, GMP, GAMP5, Annex 11, 21 CFR Part 11, Data Integrity, and computerized system validation principles.
  • Proven experience leading MES solution design, configuration, testing, deployment, and validation activities across complex projects.
  • Strong understanding of MES integration with ERP, Automation, DCS, Historians, and other manufacturing systems.
  • Demonstrated ability to lead technical discussions, conduct customer workshops, and provide strategic guidance to stakeholders.
  • Experience mentoring engineers and contributing to capability development through coaching, knowledge sharing, and technical leadership.
  • Excellent problem‑solving, communication, and stakeholder management skills, with the ability to influence decisions across projects and disciplines.

Responsibilities

  • Lead and execute complex MES implementation and optimization projects.
  • Define MES architecture, solution standards, and best practices.
  • Act as the primary technical authority and trusted advisor for MES-related decisions.
  • Drive design, configuration, testing, validation, and deployment activities.
  • Ensure compliance with GMP, GAMP5, Annex 11, 21 CFR Part 11, and Data Integrity requirements.
  • Facilitate cross‑functional collaboration between Manufacturing, QA, Automation, IT, and Business stakeholders.
  • Lead technical workshops, solution reviews, and architecture discussions.
  • Mentor and develop MES engineers and analysts through coaching and technical guidance.
  • Contribute to innovation initiatives, capability building, and continuous improvement of NNE's MES services and methodologies.
  • Support strategic business growth by identifying opportunities for standardization, digitalization, and operational excellence.

Skills

MES expertise
PAS-X
ISA-88
ISA-95
GAMP5
21 CFR Part 11
Data Integrity
ERP integration
Stakeholder management
Mentoring

Education

Bachelor's or Master's degree in Engineering, Computer Science, Life Sciences, IT

Tools

Körber PAS-X

Job description

IT Specialists
Who we are:

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.

About the role

The MES IT Specialist is a recognized subject matter expert within Manufacturing Execution Systems (MES), responsible for leading the design, implementation, validation, and continuous improvement of digital manufacturing solutions in regulated pharmaceutical environments. The role combines deep technical expertise with strategic leadership, ensuring MES solutions are compliant, scalable, and aligned with business objectives. The specialist works closely with Process Engineers, QA, Production, Automation, and IT/OT teams to translate manufacturing requirements into robust MES solutions, leveraging platforms such as PAS‑X and other industry‑standard MES technologies. In addition to driving technical excellence, the role provides mentoring, governance, and thought leadership to strengthen organizational capabilities and delivery quality across projects.

Location: Bangalore, India
Experience: 12-15 years
Department: Manufacturing Operations Management

How you might spend your days
  • Lead and execute complex MES implementation and optimization projects.
  • Define MES architecture, solution standards, and best practices.
  • Act as the primary technical authority and trusted advisor for MES-related decisions.
  • Drive design, configuration, testing, validation, and deployment activities.
  • Ensure compliance with GMP, GAMP5, Annex 11, 21 CFR Part 11, and Data Integrity requirements.
  • Facilitate cross‑functional collaboration between Manufacturing, QA, Automation, IT, and Business stakeholders.
  • Lead technical workshops, solution reviews, and architecture discussions.
  • Mentor and develop MES engineers and analysts through coaching and technical guidance.
  • Contribute to innovation initiatives, capability building, and continuous improvement of NNE's MES services and methodologies.
  • Support strategic business growth by identifying opportunities for standardization, digitalization, and operational excellence.
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 environment and enjoy working closely with colleagues, customers, and stakeholders.
  • Are passionate about digital transformation and continuously seek innovative ways to improve manufacturing processes and business outcomes.
  • Take ownership of challenges, proactively identify solutions, and drive tasks to completion with a strong sense of accountability.
  • Communicate clearly and effectively, translating complex technical topics into understandable business value.
  • Are curious, adaptable, and eager to learn new technologies, industry trends, and best practices.
  • Build trust through professionalism, integrity, and a quality‑focused mindset.
  • Enjoy mentoring others, sharing knowledge, and contributing to the growth of both individuals and teams.
  • Embrace feedback as an opportunity for continuous personal and professional development.
  • Stay motivated in complex and dynamic project environments while maintaining a positive and solution‑oriented attitude.
  • Have a strong customer focus and are committed to delivering high‑quality solutions that create lasting value.
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, Life Sciences, Information Technology, or a related discipline.
  • 12+ years of experience in Manufacturing Execution Systems (MES) within the pharmaceutical, biotech, or regulated manufacturing industry.
  • Strong hands‑on experience with MES platforms such as Körber PAS‑X or equivalent MES solutions.
  • Deep understanding of pharmaceutical manufacturing processes and electronic batch record (EBR) solutions.
  • Expert knowledge of ISA‑88, ISA‑95, GMP, GAMP5, Annex 11, 21 CFR Part 11, Data Integrity, and computerized system validation principles.
  • Proven experience leading MES solution design, configuration, testing, deployment, and validation activities across complex projects.
  • Strong understanding of MES integration with ERP, Automation, DCS, Historians, and other manufacturing systems.
  • Demonstrated ability to lead technical discussions, conduct customer workshops, and provide strategic guidance to stakeholders.
  • Experience mentoring engineers and contributing to capability development through coaching, knowledge sharing, and technical leadership.
  • Excellent problem‑solving, communication, and stakeholder management skills, with the ability to influence decisions across projects and disciplines.
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 (office), 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 August 31, 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.

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