Kwality’ was born on May 4th 1983 when its founder Mr. Ramesh Arora was inspired to begin his own venture leaving behind the already flourishing family business of spinning and aromatics. With little background of finished pharmaceuticals and high held spirits and will, he started this business. He received his first drug license in 1981 approved for liquid oral manufacturing. Climbing ladder of success, till date, Company has 48 different sections available at their production centres.
Post : Sr. Executive / Assistant Manager – QA Validation
Location : Jassur, Nurpur, Himachal Pradesh
Department : Quality Assurance – Oncology/Cytotoxic Plant
Experience : 10+ years of relevant experience in Pharmaceutical QA / Validation
Preferred : Candidates with experience in Oncology/Cytotoxic manufacturing facilities.
Qualification : B.Pharm / M.Pharm / M.Sc. or equivalent qualification in a relevant discipline.
Key Responsibilities
• Handling and execution of QA Validation activities for the Oncology/Cytotoxic manufacturing facility.
• Preparation, review and execution of Process Validation, Cleaning Validation and Equipment Qualification protocols and reports.
• Preparation and review of URS, DQ, IQ, OQ & PQ documentation.
• Review of validation data, results, deviations and conclusions.
• Handling of validation-related Change Controls, Deviations and CAPA.
• Coordination with Production, QC, Engineering and other departments for validation activities.
• Ensure compliance with cGMP, GDP, Data Integrity and regulatory requirements.
• Support internal, customer and regulatory audits related to validation.
• Ensure timely completion and closure of validation activities.
• Maintain proper validation documentation and records.
• Support periodic review and requalification activities.
• Provide technical guidance to junior team members and ensure effective implementation of QA procedures.
Key Skills
• Process Validation
• Cleaning Validation
• Equipment Qualification
• GMP / GDP
• Data Integrity
• QMS
• Change Control
• Deviation & CAPA
• Audit Compliance
• Documentation
How to Apply
Interested candidates may have thier updated CV at : hrd.hp@kwalitypharma.com
Subject Line : Application – Sr. Executive / A.M. – QA Validation
Last date : 25th September 2026
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