IT Specialist – Manufacturing Intelligence

IT Specialist Manufacturing Intelligence (Data Platforms)

Make your talent count at NNE:

We are experts in end-to-end pharma engineering and our success is built on our relationships both with our colleagues and our customers. If you want to work on projects shaping the future of sustainable and intelligent pharma facilities NNE is the place to be.

Why should you join us

You will join our PI Historian team an integral part of the Automation and IT organization in NNE collaborating closely with colleagues in Denmark and the US. Within the Manufacturing Intelligence department we have built a highly skilled and passionate team working on interdisciplinary projects in the pharmaceutical industry. Our projects range from feasibility studies and concept designs to the handover of fully operational facilities spanning large greenfield projects to medium-sized revamp and digitalization initiatives.

Location: Bangalore India
Seniority: 14 years
Department: Manufacturing Intelligence (Data Platforms)

How you might spend your days (Main Roles & Responsibilities):

As a PI Engineer youll be working with a dynamic multi-disciplinary team where your daily responsibilities include but are not limited to:

Architect implement and govern the full lifecycle (design installation configuration upgrade and retirement) of AVEVA PI System components including PI Data Archive PI Asset Framework (AF) PI Vision and critical interfaces (PI 800xA PI Batch PI to PAS-X PI BMI PI RDBMS OPC UA) within GxP-regulated manufacturing environments.
Lead validated PI server migrations and version upgrades ensuring system integrity data continuity cybersecurity compliance disaster recovery readiness and adherence to change control procedures in line with GMP requirements.
Design and oversee secure high-availability integrations between PI and pharmaceutical automation landscapes including DCS/PLC systems MES (e.g. PAS-X) LIMS ERP serialization systems and enterprise data platforms.
Own and govern the Validation (CSV) lifecycle (URS FS/DS RTM IQ/OQ/PQ FAT/SAT/UAT) ensuring compliance with GAMP 5 21 CFR Part 11 Annex 11 and ALCOA data integrity principles. Provide technical approval and audit support during regulatory inspections.
Establish and maintain validated state through robust access control models audit trail configuration backup/restore validation disaster recovery testing and periodic review processes.
Drive advanced troubleshooting and root cause analysis of PI infrastructure including interface buffering batch data consistency archive performance tuning AF optimization and system resilience improvements.
Act as global SME and escalation point across cross-functional teams (IT Automation Quality Validation Manufacturing) in multi-site pharmaceutical operations ensuring alignment with global standards and timely delivery of project milestones.
Standardize validation documentation and test management practices using enterprise tools such as TIMS (HP-ALM) ensuring traceability risk-based testing and inspection readiness.
Contribute to Pharma 4.0 and digital manufacturing initiatives by enabling real-time data visibility batch genealogy performance analytics and verification capabilities through the PI platform.
Mentor engineers and validation resources on AVEVA PI best practices regulatory expectations and sustainable system governance in GMP environments.

Who you are (Preferred Competencies)

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:

Are a strong team player with a collaborative mindset and a drive to get things done.
Are self-driven proactive and eager to make a difference in a global team.
Thrive in a dynamic cross-disciplinary environment with colleagues across Denmark the US and India.
Have robust problem-solving skills and an analytical mindset.
Are enthusiastic about learning and sharing knowledge in the field of manufacturing intelligence and automation.
The miles youve walked (Education and Work Experience)

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. Tech/B.E./M. Tech within IT Engineering or equivalent work experience
You have minimum 8 years of experience within pharma/biotech or life science industry
You have experience with large engineering projects in the industrial and or life-science sectors experience in pharmaceutical industry is an advantage
You have experience with GMP data historian systems data collection and reporting in the life science industry.

Soft skills:

Strong collaboration skills and cross cultural communication; comfortable working closely with colleagues in Denmark and the US.
Self driven exhibits strong leadership proactive and accountable; able to take ownership and deliver independently as well as in a team.
Robust problem solving and analytical mindset; able to troubleshoot complex interface/data flow issues methodically.
Quality and compliance oriented; structured documentation habits aligned with GxP validation practices.
Clear concise communicatorable to translate technical topics for non technical stakeholders.
Stakeholder management and expectation setting; builds trust through transparency and follow through.
Adaptable and organized; prioritizes effectively in fast paced multi project environments.
Continuous improvement mindset; eager to learn share knowledge and refine processes/tools.
Attention to detail with a strong sense of integrity and data stewardship.
Fluent in English (spoken and written).

Certifications:

Aveva PI System Infrastructure Specialist Aveva PI System Installation Specialist (preferred)

Were experts bound by a noble cause and driven by passion:

NNE is short for Novo Nordisk Engineering. And for all of us who work here NNE means so much more. Some of us are driven by working on highly complex projects together with other leading experts. Others are inspired by a work environment with flat hierarchy and flexible conditions. And some love the fact that they work for a world leading engineering consultancy within the pharma industry. If theres one thing we all share its the passion for what we do. Together we design and build pharma facilities that are essential for millions of patients all over the world.

Sounds like something youd like to do If youre ready to join our passion lets hear from you.

Deadline of application is 31st August 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 to your application but please include a few sentences about why you are applying in your resume or CV.

To ensure an efficient and fair recruitment process we encourage you to refrain from adding a photo in your CV. At NNE we commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

We will invite to interviews on a running basis.

To learn more about us visit

Required Experience:

IC