Quality Assurance - QMS
About the Role
Roles & Responsibilities
• Handle Quality Management System (QMS) activities as per GMP guidelines
• Manage deviations, CAPA, change control, and incident investigations
• Prepare, review, and maintain SOPs and quality documents
• Support internal audits and regulatory inspections
• Ensure compliance with regulatory standards and company quality policies
• Monitor documentation control and record management systems
Qualification
• M.Sc/ B.Pharm
Experience
• 3–6 years of experience in QA with strong exposure to QMS activities
Skills
• Strong knowledge of GMP and QMS processes
• Experience in handling deviations, CAPA, and change control
• Good documentation and review skills
• Attention to detail and compliance-focused approach
• Strong analytical and problem-solving abilities
• Effective communication and teamwork skills
About the Organization
Synthimed Labs Private Limited is a pharmaceutical manufacturing company specializing in API production with a strong focus on quality systems and regulatory compliance, offering professional growth opportunities in QA, QC, and Production domains.
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