Project Intern - Validation
Abbott
Verified
Private 1 Vacancies Both
Posted: 17 Oct 2026
|
Last date: 16 Nov 2026
17
views
Last date: 16 Nov 2026
Job Overview
Job Description
Department : QA - Validation
Primary Area : Process Validation and Validation Documentation
Job Responsibilities :The interns should be able to :
Primary Area : Process Validation and Validation Documentation
Job Responsibilities :The interns should be able to :
- Understand the overall Process Validation lifecycle.
- Understand manufacturing processes and critical unit operations.
- Support preparation and review of Process Validation Protocols (PVP).
- Participate in execution and documentation of validation batches.
- Compile and evaluate validation data.
- Understand CPPs, CQAs, IPCs and sampling requirements.
- Prepare validation documentation in accordance with GDP requirements.
- Draft Process Validation Reports (PVR) under supervision.
- Track validation activities, deviations, CAPAs and documentation status.
- Independently complete a defined validation-related project.
- Pharm D
- Fresh or previous internship experience in the same industry
How to Apply
Interested candidates can submit their CV directly using the quick apply option. Candidates can also review openings on the official Abbott website.
Direct Email Submission
Send your CV to: careers@abbott.com
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Salary / Scale
As per Govt Pay Scale
Education
As per Ad
Location
All Pakistan
Deadline
16 Nov 2026
Job Description and Requirements
Department : QA - Validation
Primary Area : Process Validation and Validation Documentation
Job Responsibilities :The interns should be able to :
Primary Area : Process Validation and Validation Documentation
Job Responsibilities :The interns should be able to :
- Understand the overall Process Validation lifecycle.
- Understand manufacturing processes and critical unit operations.
- Support preparation and review of Process Validation Protocols (PVP).
- Participate in execution and documentation of validation batches.
- Compile and evaluate validation data.
- Understand CPPs, CQAs, IPCs and sampling requirements.
- Prepare validation documentation in accordance with GDP requirements.
- Draft Process Validation Reports (PVR) under supervision.
- Track validation activities, deviations, CAPAs and documentation status.
- Independently complete a defined validation-related project.
- Pharm D
- Fresh or previous internship experience in the same industry
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