Quality Assurance - Sr. Executive / Assistant Manager

Roles & Responsibilities
• Monitor and maintain site Quality Management Systems (QMS)
• Ensure regulatory compliance with GMP and applicable global guidelines
• Support customer audits, regulatory inspections, and 483 assessments
• Prepare and review audit responses and corrective action plans
• Conduct vendor qualification and vendor evaluation activities
• Perform Nitrosamine impurities risk assessments and documentation
• Review and approve quality documents, SOPs, and change controls
• Support deviation, CAPA, and investigation management
• Coordinate with cross-functional teams to maintain quality standards
• Ensure data integrity and continuous quality improvement initiatives

Qualification
• M.Pharm (Master of Pharmacy) / M.Sc

Experience
• 6–10 years of experience in pharmaceutical Quality Assurance
• Experience in regulated markets and sterile/oncology manufacturing preferred

Skills
• Strong knowledge of GMP and global regulatory requirements
• Experience in audit management and inspection readiness
• Understanding of Nitrosamine risk assessment and compliance requirements
• Expertise in vendor qualification and quality oversight
• Strong documentation and analytical skills
• Excellent communication and stakeholder coordination ability
• Problem-solving mindset with attention to detail

About the Company
Teyro Labs Private Limited is a fast-growing CDMO specializing in oncology pharmaceuticals, focused on innovation, quality, and regulatory compliance for global regulated markets.

Walk-In Details
• Date: 22 February 2026
• Time: 9:30 AM – 3:30 PM
• Venue: Teyro Labs Private Limited, Plot No: A-9/1, SIPCOT Industrial Growth Centre, Oragadam, Chennai – 602105