Empleos

Assistant Manager, QC Lab

Posted 9 hours ago
Amneal Pharmaceuticals
Description

JOB DESCRIPTION

This role is responsible for overseeing in-process and final product quality analyses and inspections within the quality control laboratory in compliance with regulatory standards and internal specifications. The position ensures that all laboratory testing activities are conducted with accuracy and precision, interpreting results against established acceptance criteria. It plays a critical role in identifying ongoing quality issues and preventing potential production failures before they escalate. The role applies various measuring devices, testing equipment, and predetermined methodologies to accept or reject products based on defined specifications. It audits and monitors manufacturing processes and laboratory outputs against both internal and regulatory quality standards. Random sampling of finished goods is conducted to verify product conformance and laboratory integrity. Manufacturing process deviations and defects in finished goods are systematically reported and escalated for corrective action. The position contributes to continuous improvement initiatives aimed at reducing defects, rework, and quality-related costs within the Quality Control Laboratory function.

Essential Functions

  • Conduct in-process and final product quality analyses and laboratory inspections in compliance with regulatory and internal standards
  • Interpret and evaluate laboratory testing results for accuracy and precision against established specifications
  • Identify ongoing quality issues and implement preventive measures to avoid production disruptions
  • Operate measuring devices, testing equipment, and prescribed methodologies to accept or reject products
  • Audit and monitor manufacturing processes and laboratory outputs against defined internal and regulatory quality standards
  • Test random samples of finished goods to verify product conformance and laboratory integrity
  • Report manufacturing process deviations and defects in finished goods to relevant stakeholders
  • Support continuous improvement initiatives to reduce costs, defects, and rework in laboratory operations
  • Maintain documentation and records in accordance with GMP and GDP requirements

Additional Responsibilities

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

Specialized Knowledge: Licenses:
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