QA CSV & Cleaning Validation Jobs 2026 – Indore, Madhya Pradesh | Pharma Company Hiring 6–10 Years Experience

Reputed Pharma Company

Pharmaceutical Manufacturing

Job Responsibilities – QA (CSV & Cleaning Validation)

The selected candidate will be responsible for Computer System Validation (CSV), Cleaning Validation, and GMP compliance activities in the Quality Assurance department.

Computer System Validation (CSV)

• Prepare and review Validation Master Plan (VMP), URS, FS, DS, IQ, OQ, PQ, and validation reports.

• Execute Computer System Validation activities for GxP software and computerized systems.

• Ensure compliance with 21 CFR Part 11, EU Annex 11, GAMP 5, and Data Integrity requirements.

• Perform risk assessment, change control, periodic review, and system lifecycle documentation.

• Coordinate with QA, IT, Engineering, Production, and vendors during validation activities.

• Maintain validation documents and audit-ready records.

Cleaning Validation

• Prepare Cleaning Validation Protocols and Reports for manufacturing equipment.

• Perform cleaning validation studies for formulation manufacturing processes.

• Review sampling plans, recovery studies, and acceptance criteria.

• Ensure compliance with cGMP, regulatory guidelines, and SOPs.

• Investigate cleaning validation deviations and CAPA implementation.

• Support qualification and revalidation activities for equipment and cleaning processes.

Quality Assurance Responsibilities

• Ensure compliance with cGMP and pharmaceutical quality systems.

• Participate in internal audits, regulatory inspections, and documentation review.

• Review SOPs, protocols, reports, and validation documentation.

• Support continuous improvement initiatives in validation and quality systems.

Candidate Profile

• 6–10 years of experience in QA – Computer System Validation (CSV) and Cleaning Validation.

• Experience in formulation pharmaceutical manufacturing is preferred.

• Strong knowledge of 21 CFR Part 11, EU Annex 11, GAMP 5, GMP, and Data Integrity.

• Experience in validation documentation, risk assessment, and change control.

• Good communication and documentation skills.

How to Apply