Sr. Executive-QA (Validation)

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Sr. Executive-QA (Validation)

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Abryl Laboratories

time outline iconDera Bassi, Punjab, India

Posted on 24-12-2024

43 Views

1 Vacancy

Description

  • Responsible for the validation of manufacturing processes and equipment, ensuring compliance with cGMP (current Good Manufacturing Practices) and regulatory requirements.
  • Execute process validation activities, including installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ).
  • Ensure that all validation documentation is complete, accurate, and compliant with internal and regulatory standards.
  • Conduct periodic reviews and re-validation of processes to ensure ongoing compliance and effectiveness.
  • Develop, review, and execute validation protocols and reports for equipment, systems, and processes in accordance with industry standards and company guidelines.
  • Prepare protocols for new product launches and changes in existing manufacturing processes, ensuring validation requirements are met.
  • Perform qualification tests and document results accurately.

Category

Pharmaceuticals

Functional Area

Pharma Quality Assurance (QA)

Key Skills

Attention to DetailProblem solvingCommunicationTeam Work

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