Assistant Manager - QA

Roles & Responsibilities
• Lead and manage Quality Management System (QMS) activities in compliance with GMP guidelines
• Handle deviations, CAPA, change control, and risk assessment processes
• Oversee validation activities including process, cleaning, and equipment validation
• Coordinate and support internal, external, and regulatory audits
• Review and approve quality documents, SOPs, and validation protocols/reports
• Ensure timely closure of audit observations and quality issues
• Guide and mentor QA team members to maintain quality standards

Qualification
• M.Sc/ B.Pharm / M.Pharm

Experience
• 10–15 years of experience in Quality Assurance
• Strong exposure to QMS, audits, validation, and deviation management

Skills
• In-depth knowledge of GMP and regulatory requirements
• Expertise in QMS processes and audit handling
• Strong understanding of validation and quality compliance systems
• Excellent documentation and review skills
• Leadership and team management abilities
• Strong analytical, problem-solving, and communication skills

About the Organization
Synthimed Labs Private Limited is a pharmaceutical manufacturing company specializing in API production with a strong emphasis on robust quality systems and regulatory compliance, offering leadership opportunities in QA, QC, and Production functions.