Senior Executive, QMS

Amneal Pharmaceuticals; Ahmedabad District; On-site; INR 800,000 - 1,600,000; Full time

Job summary

Amneal Pharmaceuticals in India is seeking a Quality Assurance professional to independently conduct investigations for product quality complaints, deviations, and related events, ensuring timely closure and regulatory compliance.

The role involves root cause analysis, CAPA initiation and verification, and coordination of change controls, with emphasis on data integrity and cross-functional collaboration to drive continuous improvement.

Qualifications

• Strong understanding of QMS principles and compliance.
• Knowledge of GMP, cGMP, GLP, GDP and regulatory requirements from agencies such as FDA/EMA/WHO.
• Strong attention to detail to identify documentation errors and ensure data integrity.
• Strong written and verbal communication skills for reports and discussions.

Responsibilities

• Independently conduct and prepare investigation reports for Product Quality Complaints, Unplanned Deviations, OOS, OOT, and OOAL events.
• Perform root cause analysis using appropriate tools and recommend CAPA.
• Initiate, review, track, and verify CAPA implementation and effectiveness.
• Review and coordinate Change Controls with QA/regulatory impact assessments.
• Analyze and prepare annual trend reports to identify recurring issues and drive improvement.
• Prepare Quality Metrics and Management Review reports for site leadership.
• Maintain QMS records in compliance with cGMP and ALCOA+ data integrity.
• Support internal and regulatory audits and inspections.
• Assist in SOP development/revision and cross-functional collaboration to resolve quality issues.

Skills

QMS principles

Attention to detail

Written and verbal communication

Education

B. Pharm

M. Pharm

Job description

Description

• Independently conduct and prepare investigation reports for Product Quality Complaints, Unplanned Deviations, OOS, OOT, and OOAL events, ensuring timely closure and regulatory compliance.
• Perform root cause analysis using appropriate tools (5-Why, Fishbone, Risk Assessment, etc.) and recommend effective corrective and preventive actions (CAPA).
• Initiate, review, track, and verify CAPA implementation and effectiveness within established timelines.
• Review and coordinate Change Controls related to processes, equipment, facilities, systems, materials, and documentation, including quality and regulatory impact assessments.
• Analyze and prepare annual trend reports for Unplanned Deviations, Complaints, CAPAs, OOS, OOT, and OOAL events to identify recurring issues and drive continuous improvement.
• Prepare Quality Metrics, Management Review reports, and periodic trend analyses for site leadership.
• Maintain QMS records in compliance with cGMP, Data Integrity (ALCOA+), and company procedures.
• Support internal audits, customer audits, and regulatory inspections.
• Assist in the development, review, and revision of SOPs and other quality system documents.
• Collaborate with Manufacturing, Quality Control, Engineering, Validation, and other cross-functional teams to resolve quality issues.
• Support inspection readiness initiatives and promote continuous improvement of Quality Management Systems.
• Ensure all activities are performed in compliance with applicable cGMP, FDA, ICH, company policies, and Health & Safety requirements.

JOB DESCRIPTION

• Independently conduct and prepare investigation reports for Product Quality Complaints, Unplanned Deviations, OOS, OOT, and OOAL events, ensuring timely closure and regulatory compliance.
• Perform root cause analysis using appropriate tools (5-Why, Fishbone, Risk Assessment, etc.) and recommend effective corrective and preventive actions (CAPA).
• Initiate, review, track, and verify CAPA implementation and effectiveness within established timelines.
• Review and coordinate Change Controls related to processes, equipment, facilities, systems, materials, and documentation, including quality and regulatory impact assessments.
• Analyze and prepare annual trend reports for Unplanned Deviations, Complaints, CAPAs, OOS, OOT, and OOAL events to identify recurring issues and drive continuous improvement.
• Prepare Quality Metrics, Management Review reports, and periodic trend analyses for site leadership.
• Maintain QMS records in compliance with cGMP, Data Integrity (ALCOA+), and company procedures.
• Support internal audits, customer audits, and regulatory inspections.
• Assist in the development, review, and revision of SOPs and other quality system documents.
• Collaborate with Manufacturing, Quality Control, Engineering, Validation, and other cross-functional teams to resolve quality issues.
• Support inspection readiness initiatives and promote continuous improvement of Quality Management Systems.
• Ensure all activities are performed in compliance with applicable cGMP, FDA, ICH, company policies, and Health & Safety requirements.

Additional Skills

• Strong understanding of QMS principles and compliance.
• Knowledge of GMP, cGMP, GLP, GDP, and regulatory requirements from agencies such as the U.S. Food and Drug Administration , European Medicines Agency , and World Health Organization .
• Strong attention to detail to identify documentation errors and ensure data integrity.
• Strong written and verbal communication skills for preparing reports, leading discussions, and driving quality initiatives.

Education

QUALIFICATIONS

• B. Pharm B. Pharm - Required
• M. Pharm M. Pharm - Preferred

Experience

• 5 years or more in 5 - 8 Years

Specialized Knowledge: Licenses: