We are looking for a QA Executive with hands-on experience in Validation Qualification activities in a pharmaceutical manufacturing workplace The candidate should have strong knowledge of GMP requirements and regulatory guidelines and be capable of handling validation documentation and compliance activities independently Key Responsibilities Plan execute and review Validation Qualification activities DQ IQ OQ PQ Preparation review and approval of validation protocols and reports for equipment utilities systems and processes Handle cleaning validation process validation and re-validation activities Ensure compliance with cGMP Schedule M WHO and regulatory guidelines Coordinate with production engineering QC and other departments during validation activities Review change controls deviations CAPA and risk assessments related to validation Support internal and external audits and regulatory inspections Maintain proper documentation and records as per QA requirements Required Qualifications B Pharm M Pharm M Sc or equivalent qualification 2-5 years of relevant experience in QA Validation Qualification in a pharma company Strong understanding of GMP validation lifecycle and regulatory compliance Good documentation analytical and communication skills Preferred Skills Exposure to audits and regulatory inspections Knowledge of HVAC water systems and computerized system validation CSV is an added advantage Ability to work independently and as part of a cross-functional team Interested candidates can send their CV to hrd fidopharma com OR (phone hidden) Job Type Permanent Pay 20 000 00 - 40 000 00 per month Benefits Health insurance Provident Fund Work Location In person