Job Opportunity with Accenture For MES Digital Lifescience

from 7 to 12 year(s) of Experience
Not Disclosed by Recruiter
Posted: 23 days agoJob Applicants: 784+Job Views: 2170+

Job Description


Level- Manager, Consultant

Experience-6 to 12 Years

Location- Gurgaon

  • Must have exposure to the Life Sciences industry mainly in the following areas:

    • Pharmaceuticals

    • Biotechnology

    • Medical products and devices

  • Experience in providing services such as large-scale business and technology transformation, targeted business performance improvement and post-merger integration for R&D functions (includes Pharmacovigilance, Clinical, Regulatory, Pre-clinical and research, QC and research laboratories).

  • Profound understanding of global regulations and Health Authorities expectations governing computerized systems incl. computerized systems validation, lifecycle management and 21 CFR Par 11 requirements.

  • Profound experience in the development, implementation and lifecycle management of key computerized systems in the Pharmaceutical Development, Manufacturing and Quality space (e.g. ERP/SAP, CTMS, MES, LIMS) 


MES/MOM Understanding:

 Experience includes the development of GUI, Workflows, Phase, Equipment management, Equipment management with run-time properties, Labels and Reports using Jasper reports, Use-cases, Flexible state model, EIG transaction, LIMS integration and Data Migration used in MES solutions

  • Deployment experience with plant floor/Manufacturing Execution Systems (MES) solutions (e.g. Rockwell ProPack Data, Werum PAS-X, POMS) is a must.

  • Knowledge of SAP Material Master (MM), Production Planning (PP), Production Planning for the Process Industry (PP/PI) and Quality Management (QM) modules is highly preferred.

  • Experience with FactoryTalk Production Centre, PharmaSuite, LabWare LIMS, and PI-Historian is highly desirable. Automation Software experience with RSLogix 5000, FactoryTalk® Batch PlantPAx are helpful. Also, Experience with .NET technologies preferred

  • Knowledge of FDA, EU, and global GMP's including Good Automated Manufacturing Practices, 21 CFR Part 11, and EU cGMP Annex 11. Relevant Quality education or training within ISO 9001 and cGMP is highly preferred.

  • Validation experience in the Life Science / Pharmaceutical industry required. Ensure that the system remains in a validated state and that proper change control practices are followed (CCRs, documents updates....etc.).

  • Experience integrating ANSI/ISA-88 and ANSI/ISA-95 standards where the MES is integrated into the Batch Execution System (BES)

Salary: Not Disclosed by Recruiter

Industry:Pharma / Biotech / Clinical Research

Functional Area:Other

Employment Type:Full Time, Permanent


Desired Candidate Profile

Please refer to the Job description above

Company Profile

Accenture Solutions Pvt Ltd

Accenture is a leading global professional services company, providing a broad range of services in strategy and consulting, interactive, technology and operations, with digital capabilities across all of these services. We combine unmatched experience and specialized capabilities across more than 40 industries €" powered by the world€™s largest network of Advanced Technology and Intelligent Operations centers. With 505,000 people serving clients in more than 120 countries, Accenture brings continuous innovation to help clients improve their performance and create lasting value across their enterprises. Visit us at
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Recruiter Name:Accenture HR Team

Contact Company:Accenture Solutions Pvt Ltd