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MES Consultant - Camstar

Capgemini

Location

Mumbai (ex Bombay), IN

Salary

Not disclosed

Employment

Other

Experience

10-14 years

Job overview

Complete role details

Location

Mumbai (ex Bombay), IN

Employment type

Other

Workplace

Onsite

Experience

10-14 years

Seniority

Individual Contributor

Education

Bachelor's degree

Skills

SQL

Role details

Job description

Job Description

MES Consultant (Siemens Camstar / Critical Manufacturing MES) – Medical Devices

Location: PAN India
Experience: 10–14 Years

Choosing Capgemini means choosing a company where you'll be empowered to shape your career, supported by a collaborative global community, and inspired to reimagine what's possible. Join us in helping leading Life Sciences and Medical Device organizations accelerate their digital manufacturing transformation through MES, Smart Factory, and Industry 4.0 initiatives.

Role Overview

We are seeking an experienced MES Consultant with expertise in Siemens Camstar and/or Critical Manufacturing MES to support digital manufacturing and smart factory initiatives within the Medical Devices and Life Sciences industry.

The ideal candidate will have strong experience in MES implementation, configuration, validation, system integration, and manufacturing process optimization in regulated environments. This role requires collaboration with manufacturing, quality, validation, and IT teams to deliver compliant and scalable MES solutions that support operational excellence and regulatory requirements.

Key Responsibilities

• Lead MES implementation, upgrade, enhancement, and support projects using Siemens Camstar and/or Critical Manufacturing MES.

• Gather, analyze, and document business requirements and translate them into MES solutions aligned with Life Sciences manufacturing processes.

• Configure and support MES functionalities including Electronic Batch Records (EBR), Weigh & Dispense, Genealogy, Traceability, Quality Management, and Production Execution.

• Integrate MES with ERP, LIMS, SCADA, Automation Systems, Historians, and Serialization platforms.

• Support Computer System Validation (CSV) activities and ensure compliance with GxP, GMP, GAMP5, and FDA 21 CFR Part 11 requirements.

• Participate in solution design, testing, deployment, go-live, hypercare, and post-production support activities.

Ideal Candidate Profile

10–14 years of experience in MES, Manufacturing IT, Digital Manufacturing, or Smart Manufacturing environments.

• Hands-on experience with Siemens Camstar and/or Critical Manufacturing MES platforms.

• Strong understanding of Life Sciences, Medical Devices, Pharmaceuticals, or Biotechnology manufacturing processes.

• Knowledge of Electronic Batch Records (EBR), Genealogy, Traceability, Quality Management, and Production Execution processes.

• Experience integrating MES with ERP, LIMS, SCADA, Automation Systems, and enterprise applications.

• Strong knowledge of SQL, APIs, Web Services, and manufacturing data management.

Preferred Qualifications

• Bachelor's degree in Engineering, Information Technology, Computer Science, or a related field.

• Experience within Medical Devices, Pharmaceuticals, Biotechnology, or Life Sciences industries.

What You'll Love About Working Here

You'll work on large-scale digital manufacturing and MES transformation programs for leading Life Sciences and Medical Device organizations.

About Us

At Capgemini Engineering, the world leader in engineering and R&D services, we bring together a global team of engineers, scientists, software experts, and architects to help the world's most innovative organizations unlock their potential through technology and engineering excellence.