Deputy Manager Quality Control

Amneal Pharmaceuticals; Ahmedabad District; On-site; INR 1,800,000 - 3,000,000; Full time

Job summary

Amneal Pharmaceuticals LLC seeks a QC Quality Lead in India (Gujarat) to oversee in-process and finished product testing and ensure compliance with regulatory standards. You will interpret results, identify trends, and lead investigations into deviations while developing the QC team and supporting audits.

The role emphasizes continuous improvement, CAPA, training, and robust documentation to maintain product quality across manufacturing processes.

Qualifications

• Oversee in-process and finished product quality control testing activities
• Interpret analytical results against approved specifications and standards
• Identify quality trends, deviations, and potential production risks
• Audit and monitor manufacturing processes for quality compliance
• Lead investigation of deviations, defects and non-conformances
• Drive continuous improvement initiatives within QC operations
• Build team capability through Training and Competency Management

Responsibilities

• Oversee in-process and finished product quality control testing activities
• Interpret analytical results against approved specifications and standards
• Identify quality trends, deviations, and potential production risks
• Audit and monitor manufacturing processes for quality compliance
• Review and approve analytical data, reports, and COA documentation
• Lead investigation of deviations, defects and non-conformances
• Ensure compliance with GMP, GLP, and regulatory requirements
• Manage and develop QC team performance and competency
• Support internal and external audits and regulatory inspections
• Drive continuous improvement initiatives within QC operations
• Build team capability through Training and Competency Management

Skills

Quality control testing

Analytical results interpretation

Deviations investigation

GMP/GLP compliance

Audit & compliance

Team leadership

Training & competency management

Continuous improvement

Education

M.Sc.

M.Pharm

Job description

Job Description:

Description:

The role is responsible for ensuring in-process and final product quality analyses in compliance with regulatory standards and internal specifications. The role focuses on interpreting and evaluating analytical results for accuracy and precision against established criteria. The role involves identifying recurring quality issues, preventing potential production risks, and recommending continuous improvement actions. The position uses validated testing equipment, measuring devices, and prescribed methods to accept or reject materials and products. As a people leader, the role audits and monitors manufacturing processes, oversees random testing of finished goods, and ensures timely reporting of deviations and defects to maintain product quality and compliance.

Essential Functions:

• Oversee in-process and finished product quality control testing activities
• Interpret analytical results against approved specifications and standards
• Identify quality trends, deviations, and potential production risks
• Ensure acceptance or rejection of materials and products based on test results
• Audit and monitor manufacturing processes for quality compliance
• Review and approve analytical data, reports, and COA documentation
• Lead investigation of deviations, defects and non-conformances
• Ensure compliance with GMP, GLP, and regulatory requirements
• Manage and develop QC team performance and competency
• Support internal and external audits and regulatory inspections
• Drive continuous improvement initiatives within QC operations
• Build team capability through Training and Competency Management

Qualifications

Education: M. Sc. - Required /M. Pharm - Preferred

Experience: 10 to 15 Years