Project Intern - Validation

This internship opportunity within the QA - Validation department focuses on gaining hands-on experience in process validation and related documentation. The role is designed to provide a comprehensive understanding of the process validation lifecycle, manufacturing processes, and critical unit operations. Interns will actively support the preparation and review of process validation protocols, participate in the execution and documentation of validation batches, and compile and evaluate validation data. The position also involves understanding key quality parameters such as CPPs, CQAs, IPCs, and sampling requirements, while ensuring that all validation documentation complies with Good Documentation Practices (GDP). Under supervision, interns will draft process validation reports and track validation activities, deviations, CAPAs, and documentation status. Additionally, interns are expected to independently complete a defined validation-related project during their tenure.

Key Responsibilities:
- Understand the overall process validation lifecycle.
- Gain knowledge of manufacturing processes and critical unit operations.
- Support the preparation and review of Process Validation Protocols (PVP).
- Participate in the execution and documentation of validation batches.
- Compile and evaluate validation data effectively.
- 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.
- Track validation activities, deviations, Corrective and Preventive Actions (CAPAs), and documentation status.
- Complete an independent validation-related project within the internship period.

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

Preferred Qualifications and Benefits:
- The internship duration is 5 to 6 months.
- Compensation details vary by location and are not specified here.
- The position is based in Karachi, Pakistan, within the Established Pharma Division (EPD).
- Standard work shift applies.
- No specific travel or medical surveillance requirements are indicated.

This role offers valuable exposure to quality assurance processes within a regulated pharmaceutical environment, ideal for candidates seeking to build a career in process validation and quality documentation.