Assistant Manager QA Validation

Amneal Pharmaceuticals LLC; Ahmedabad District; On-site; INR 1,800,000 - 2,400,000; Full time

Job summary

Amneal Pharmaceuticals LLC seeks a Quality Assurance leader for validation programs across manufacturing operations. You will define activities, build infrastructure, lead QA professionals, and ensure compliance with GMP and regulatory standards.

Responsibilities include audits, process improvements, vendor coordination, and timely resolution of validation issues, with focus on reducing defects and maintaining validated processes.

Qualifications

• Bachelor's degree in science or related field is required.
• Master's degree in science is preferred.
• 8+ years of experience in validation quality assurance in pharmaceutical manufacturing.

Responsibilities

• Define and specify quality activities, processes, and standards for validation programs in compliance with regulatory requirements
• Build and maintain quality infrastructure and systems to ensure timely delivery of validated and compliant pharmaceutical products
• Lead and manage a team of quality professionals to deliver validation quality assurance objectives
• Conduct audits and monitoring of validation activities and manufacturing processes against internal and regulatory standards
• Ensure efficient workflow, procedures, policies, and validation inspection programs are implemented and maintained across manufacturing operations
• Manage in-process product quality and validation outcomes in coordination with vendors and contract manufacturers
• Communicate with customers and vendors to investigate and resolve quality and validation-related issues in a timely manner
• Report and troubleshoot manufacturing process deviations and defects identified during validation studies and finished goods inspection
• Identify and implement process improvements to reduce costs, defects, errors, and rework in validation and manufacturing operations

Education

Bachelors Degree (BA/BS) B. Sc. - Required

Master Degree (MS/MA) M. Sc.. - Preferred

Job description

Job Description:

JOB DESCRIPTION

This role is responsible for defining and specifying the activities, processes, and standards required to fulfill quality requirements for manufactured materials, components, and products within a global pharmaceutical environment. The position builds and maintains the infrastructure and systems necessary to consistently ensure the timely delivery of quality-compliant products. It leads and manages validation quality assurance activities to ensure manufacturing processes and equipment meet defined regulatory and internal standards. The role ensures efficient and effective workflows, procedures, policies, and validation programs are in place and adhered to across manufacturing operations. It manages in-process product quality in coordination with vendors and contract manufacturers. The position facilitates communication with customers and vendors to resolve quality-related issues in a timely and compliant manner. It reports and troubleshoots manufacturing process deviations and defects identified in finished goods and validation studies. The role leads a team of quality professionals and contributes to continuous improvement initiatives aimed at reducing defects, errors, and rework across manufacturing operations. It also supports the development and maintenance of validation master plans and related documentation.

Essential Functions

• Define and specify quality activities, processes, and standards for validation programs in compliance with regulatory requirements
• Build and maintain quality infrastructure and systems to ensure timely delivery of validated and compliant pharmaceutical products
• Lead and manage a team of quality professionals to deliver validation quality assurance objectives
• Conduct audits and monitoring of validation activities and manufacturing processes against internal and regulatory standards including 21 CFR Part 210 & 211 and GMP guidelines
• Ensure efficient workflow, procedures, policies, and validation inspection programs are implemented and maintained across manufacturing operations
• Manage in-process product quality and validation outcomes in coordination with vendors and contract manufacturers
• Communicate with customers and vendors to investigate and resolve quality and validation-related issues in a timely manner
• Report and troubleshoot manufacturing process deviations and defects identified during validation studies and finished goods inspection
• Identify and implement process improvements to reduce costs, defects, errors, and rework in validation and manufacturing operations

QUALIFICATIONS

Education

• Bachelors Degree (BA/BS) B. Sc. - Required
• Master Degree (MS/MA) M. Sc.. - Preferred

Experience

• 8 years or more in 8 - 10 Years