Amneal India

Senior Executive, Lab QA

Amneal India Ahmedabad, Gujarat, India

Pharmaceutical Manufacturing · 5,001-10,000 employees

7 h ago
qa Senior (5-10 yrs) Full-time India
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About the role

This role defines and maintains quality standards and infrastructure for laboratory operations within a global pharmaceutical environment. It involves conducting audits, managing vendor quality, and troubleshooting manufacturing process deviations to ensure regulatory compliance.

What they look for

Quality Assurance Laboratory Operations GMP 21 CFR Part 210 21 CFR Part 211 Pharmaceutical Manufacturing Auditing Process Improvement Vendor Management Compliance Quality Control Deviation Management Root Cause Analysis Regulatory Standards Laboratory Inspection

Requirements

The position requires a Bachelor of Pharmacy degree, with a Master of Pharmacy preferred. Candidates must possess 5 to 8 years of relevant experience in laboratory quality assurance and pharmaceutical manufacturing.

Full description

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 supports the auditing, monitoring, and evaluation of laboratory quality activities against defined internal and regulatory standards. The role ensures efficient and effective workflows, procedures, policies, and laboratory inspection programs are in place and adhered to across quality laboratory 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. The role contributes to continuous improvement initiatives aimed at reducing defects, errors, and rework across laboratory and manufacturing operations. It also supports the identification and development of outsourcing vendors and suppliers according to organizational quality standards.

Essential Functions:• Define and specify quality activities, processes, and standards for laboratory quality assurance programs in compliance with regulatory requirements

  • Build and maintain quality infrastructure and systems to ensure timely delivery of compliant pharmaceutical products
  • Conduct audits and monitoring of laboratory quality activities and outputs against internal and regulatory standards including 21 CFR Part 210 & 211 and GMP guidelines
  • Ensure efficient workflow, procedures, policies, and laboratory inspection programs are implemented and maintained across quality laboratory operations
  • Manage in-process product quality in coordination with vendors and contract manufacturers to meet defined quality specifications
  • Communicate with customers and vendors to investigate and resolve quality and laboratory-related issues in a timely manner
  • Report and troubleshoot manufacturing process deviations and defects identified in laboratory testing and finished goods
  • Identify and implement process improvements to reduce costs, defects, errors, and rework in laboratory and manufacturing operations
  • Support the identification and development of outsourcing vendors and suppliers according to organizational quality standards and policies

Additional Responsibilities:

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