MES Validation SME (Rockwell MES)

SIRO Clinpharm Pvt. Ltd.; India; On-site; INR 4,000,000 - 7,000,000; Full time

Job summary

SIRO Clinpharm Pvt. Ltd. is seeking an experienced MES Validation SME to validate Rockwell PharmaSuite implementations Pan India. You will lead CSV activities, develop validation protocols, review documentation and coordinate cross-functional teams.

The ideal candidate has 8+ years in MES validation, strong GxP knowledge and hands-on expertise with ALM/qTest, EBR, and ERP/LIMS integrations.

Qualifications

• Must have 8+ years of experience in MES validation and CSV
• Strong knowledge of GxP/GMP regulatory requirements
• Hands-on experience with Rockwell PharmaSuite and related integration tools

Skills

Rockwell PharmaSuite / MES Validation

Computer System Validation (CSV)

GxP/GMP

Recipe Management

Workflow Configuration

EBR

Material Management & Production

SDLC / UAT / Test Execution

ALM/qTest, Agile Methodology

ERP / LIMS & Automation Integration

Tools

ALM/qTest

ERP

LIMS

Job description

Job Title: MES Validation SME Rockwell PharmaSuite

Location: Pan India

Experience: 8+ Years

Required Skills:

• Rockwell PharmaSuite / MES Validation
• Computer System Validation (CSV), GxP/GMP
• Recipe Management, Workflow Configuration, EBR
• Material Management & Production Execution
• SDLC, UAT, Test Execution & Validation Documentation
• ALM/qTest, Agile Methodology
• ERP, LIMS & Automation Integration