Job Summary We are seeking a detail-oriented and experienced QA - QMS Specialist to support and maintain our Quality Management System QMS This role is critical in ensuring our organization remains compliant with industry standards and regulatory requirements The ideal candidate will have a strong understanding of QMS processes document control audits CAPA systems and continuous improvement methodologies Key Responsibilities Manage and maintain QMS documentation including SOPs work instructions and quality records Support internal and external audits ISO FDA customer etc Monitor and track non-conformances deviations CAPAs and change controls Collaborate with cross-functional teams to ensure QMS compliance and improvement Assist in training staff on quality procedures and QMS updates Prepare reports and metrics related to QMS performance and trends Ensure compliance with regulatory and industry standards such as ISO 9001 ISO 13485 FDA 21 CFR Part 11 820 or other applicable standards Participate in root cause analysis and risk assessments Qualifications Bachelor s degree in a science engineering or quality-related field preferred 2-7 years of experience in QA QMS within Pharmaceuticals industry Solid knowledge of QMS frameworks e g ISO FDA ICH Q10 Experience with audit preparation and hosting Proficient in quality tools such as CAPA FMEA and RCA Solid organizational and communication skills Familiarity with electronic QMS software e g Master Control Veeva Track Wise is a plus Interested candidates share me your on rahul gmh co in Job Types Full-time Permanent Pay 25 000 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)

📌 Qa (qms) (Baddi)
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