Validation Specialist

Thompsons HR Consulting Pvt Ltd; Hyderabad; On-site; INR 1,200,000 - 2,500,000; Full time

Job summary

Thompsons HR Consulting Pvt Ltd seeks a seasoned Validation Specialist for Hyderabad. The candidate should have 10+ years in Pharma/FMCG validation, with strong hands-on Process, Cleaning, and Equipment Qualification experience and CSV exposure.

Role includes leading site-level/multi-site validation projects, preparing protocols and reports, and ensuring compliance with cGMP/FDA/WHO standards. Work from office for a one-year contract.

Qualifications

• 10+ years in Pharma/FMCG validation domains.
• Hands-on experience across validation lifecycle activities.
• Strong knowledge of VMP and validation SOPs.

Responsibilities

• Lead site-level validation projects and multi-site programs.
• Prepare validation protocols and validation reports.
• Coordinate with QA, manufacturing and laboratories to ensure compliance.

Skills

Pharma Validation

FMCG Validation

Process Validation

Cleaning Validation

IQ/OQ/PQ

Utility Validation

Laboratory Validation

Analytical Method Validation

CSV

Validation Protocols

Validation Reports

Validation Master Plan

GAMP 5

CAPA

Coordination

Project Management

Tools

ISO/GAMP 5 Tools

Job description

• 10+ years of experience in Pharma / FMCG Validation
• Strong hands-on experience in Process Validation
• Cleaning Validation
• Equipment Qualification IQ/OQ/PQ
• Utility Validation / Qualification
• Laboratory & Analytical Method Validation
• Computer System Validation (CSV)
• Experience preparing Validation Protocols & Validation Reports
• Strong knowledge of Validation Master Plan (VMP)
• Good knowledge of cGMP, FDA, WHO, ISO & GAMP 5
• Experience in Validation Risk Assessment, Deviations & CAPA
• Experience leading site-level / multi-site validation projects
• Strong documentation, coordination and project management skills

Job Role:

Validation Specialist

Location:

Hyderabad

Experience:

10+ Years

Contract:

1 Year

Work Mode:

Work from Office

Key Skills Required

• 10+ years of experience in Pharma / FMCG Validation
• Strong hands-on experience in Process Validation
• Cleaning Validation
• Equipment Qualification IQ/OQ/PQ
• Utility Validation / Qualification
• Laboratory & Analytical Method Validation
• Computer System Validation (CSV)
• Experience preparing Validation Protocols & Validation Reports
• Strong knowledge of Validation Master Plan (VMP)
• Experience developing Validation SOPs & Standards
• Good knowledge of cGMP, FDA, WHO, ISO & GAMP 5
• Experience in Validation Risk Assessment, Deviations & CAPA
• Experience leading site-level / multi-site validation projects
• Strong documentation, coordination and project management skills