Sr. Executive-QA (Validation)
0 - 5 Years of ExperienceNot disclosed Full Time
Abryl Laboratories
Dera 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
Aggregated job.
Learn more