BENGALURU · FULLTIME
Associate MES Engineer
NNE
Bengaluru · onsite · Posted 29d ago
Sourced from
Undisclosed3–5 yrsfulltimeBengaluru
About a minute. You'll make an account on the way through.
agent · working
- Read this posting0.2s
- Found the form on Naukri · 7 questions to answer1.7s
- Decided the answers for all of them3.1s
- Tailor your résumé to this role
- Waiting for you
Section · 01
About this role
Job Summary
Responsibilities
Who You Are
Requirements
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
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
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 K rber 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
- 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.
Requirements
- 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 K rber 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.
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Section · 02
Skills
AutomationCfrBIOTECHdigital manufacturingbatch managementBusiness Requirementsmanufacturing executionLearning And Developmentdeploymentmanufacturing execution systemsManufacturingInformation TechnologyLife Sciences
Section · Company
About NNE
NNE
Engineering & Construction
400
employees
1996
30 years old
Bangalore / Bengaluru, Karnataka
India
₹12.8L PA avg
Avg at NNE
About
NNE that focuses on end-to-end engineering services tailored specifically towards the pharmaceutical industry.
Industries
Engineering & ConstructionBiotech & Life sciences
Employee ratings
10 reviews
3.4/ 5
Culture
3.5
Career growth
2.3
Work-life
3.1
Employees rate it well for
Work-Life Balance39Company Culture35
Find them on