Project Intern - Validation

This internship opportunity is designed for candidates interested in gaining hands-on experience in the field of Process Validation within the Quality Assurance (QA) - Validation department. The role focuses on understanding and supporting various stages of the Process Validation lifecycle, including manufacturing processes, critical unit operations, and validation documentation. Interns will actively participate in preparing and reviewing validation protocols, executing validation batches, and compiling data to ensure compliance with Good Documentation Practices (GDP). This position offers a chance to work closely with validation activities, track deviations and corrective actions, and independently manage a defined validation-related project, providing a comprehensive learning experience in a regulated industry environment.

Key Responsibilities:
- Gain a thorough understanding of the overall Process Validation lifecycle.
- Learn and comprehend manufacturing processes and critical unit operations.
- Assist in the preparation and review of Process Validation Protocols (PVP).
- Participate in the execution and documentation of validation batches.
- Compile and evaluate validation data to support quality decisions.
- Understand Critical Process Parameters (CPPs), Critical Quality Attributes (CQAs), In-Process Controls (IPCs), and sampling requirements.
- Prepare validation documentation in compliance with Good Documentation Practices (GDP).
- Draft Process Validation Reports (PVR) under supervision.
- Monitor and track validation activities, deviations, Corrective and Preventive Actions (CAPAs), and documentation status.
- Complete a defined validation-related project independently, demonstrating applied knowledge and problem-solving skills.

Required Qualifications:
- Pharm D degree.
- Fresh graduates or candidates with prior internship experience in the pharmaceutical or related industry.

Duration:
The internship is structured for a period of 5 to 6 months, providing sufficient time to develop practical skills and industry knowledge.

This internship is ideal for individuals seeking to build a strong foundation in process validation and quality assurance within a pharmaceutical manufacturing setting. It offers exposure to real-world validation processes and documentation standards, preparing candidates for future roles in quality control, validation, and regulatory compliance.