Key Responsibilities Execute and review validation protocols IQ OQ PQ for equipment utilities and systems used in sterile injectable manufacturing Perform process validation cleaning validation and hold time studies Prepare review and maintain validation-related documents as per cGMP and regulatory requirements Coordinate with cross-functional teams including Production QC Engineering and Regulatory Affairs during validation activities Participate in qualification of HVAC WFI PW compressed air systems autoclaves and filling line equipment Support regulatory audits EU WHO etc and provide necessary validation documentation Ensure compliance with data integrity and good documentation practices Qualifications B Pharm M Pharm M Sc in a relevant field 4-6 years of experience in QA Validation within a sterile injectables manufacturing environment Strong understanding of regulatory guidelines MHRA EU GMP Proficient in documentation protocol writing and deviation investigation handling Good interpersonal and communication skills Preferred Skills Experience with aseptic processes and cleanroom validation Familiarity with computerized system validation CSV Knowledge of risk assessment tools like FMEA Employment Type Full-Time Work Location Baddi Jharmajri Salary 30000 to 45000 To Apply Please send your updated CV to rahul gmh co in or WhatsApp (phone hidden) Job Types Full time Permanent Pay 30 000 00 - 40 000 00 per month Benefits Cell phone reimbursement Flexible schedule Food provided Health insurance Internet reimbursement Leave encashment Life insurance Paid sick time Paid time off Provident Fund Work Location In person Speak with the employer 91 (phone hidden)