Job Description We are looking for an experienced and detail-oriented QA Manager to join our team in an Injectable Pharma Plant. The ideal candidate should possess strong knowledge of pharmaceutical quality systems, regulatory compliance, and hands-on exposure to validation activities. Key Responsibilities: Lead QA operations in an Injectable Pharma Plant ensuring compliance with cGMP and regulatory requirements. Handle complete validation activities including Autoclave, DHS, and HVAC validations. Monitor and ensure compliance of Media Fill, Temperature Mapping and other critical processes. Manage QMS activities such as Change Control, Deviations, CAPA and ensure timely closure. Act as the front face during audits/inspections and ensure effective CAPA implementation post audit. Ensure adherence to Good Documentation Practices (GDP) and prepare, review, and update SOPs . Conduct training sessions for employees on new/revised SOPs. Coordinate with Microbiology & QC departments and provide basic technical support. Desired Candidate Profile: Minimum 5 years of experience in QA in an Injectable Pharma Plant. Strong knowledge of QMS, regulatory compliance, and validation activities . Excellent communication and leadership skills. Ability to lead audits and represent the organization effectively. Team-oriented professional with attention to detail. Perks and Benefits: Competitive Salary [Insert Range if applicable] Growth and learning opportunities in a reputed organization Exposure to regulatory audits and international compliance standards
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