Pharmaron is looking for a Software Validation Intern to gain hands-on experience in a GLP/GMP-regulated environment, learning how validated software supports laboratory operations in the life sciences industry.
Requirements
- Prior experience with database systems, software testing, or validation documentation is a plus - but not required.
Responsibilities
- Support the Software Validation Engineer through all stages of the software validation lifecycle - including planning, testing, and documentation.
- Assist with creating and maintaining key validation documents such as risk assessments, test scripts, validation protocols, and reports.
- Learn how to evaluate software systems for compliance with FDA and international guidelines (including 21 CFR Part 11 and GAMP 5).
- Participate in audit readiness activities and learn how validation supports data integrity and laboratory compliance.
- Collaborate with scientists, engineers, and quality professionals to understand how software systems integrate into research operations.
- Contribute to the development or revision of Standard Operating Procedures (SOPs) and other quality documentation.
Other
- Bachelor's degree in Information Technology, Computer Science, Bioinformatics, Engineering, or a related field.
- Interest in software validation, data integrity, or compliance within a life sciences or technology setting.
- Strong organizational and analytical skills with attention to detail.
- Excellent communication and teamwork abilities.
- Six months, full-time
