Equipment Validation Engineer
Virtue America
Minnesota, United States0–2 yrs51m agovia LinkedIn
About the Role
We are seeking an Entry-Level Equipment Validation Engineer to support equipment qualification and validation activities in a GMP-regulated pharmaceutical or life sciences manufacturing environment. This role is ideal for recent graduates looking to build a career in validation and compliance.
Key Responsibilities
- Assist with execution of IQ, OQ, and PQ protocols for manufacturing and laboratory equipment
- Support equipment installation, commissioning, and qualification activities
- Prepare and maintain validation documentation and reports
- Assist with deviation investigations, change controls, and CAPA activities
- Ensure compliance with GMP, FDA regulations, and Good Documentation Practices (GDP)
- Collaborate with Engineering, QA, Manufacturing, and Validation teams
- Support audit and inspection readiness
Requirements & Tech Stack
- Bachelor's degree in Mechanical, Chemical, Biomedical, Electrical Engineering, Biotechnology, Pharmacy, or related field
- 0–2 years of validation or engineering experience (internships/co-ops accepted)
- Basic understanding of validation lifecycle and GMP regulations
- Strong technical writing and analytical skills
Qualifications
- Knowledge of equipment qualification and validation concepts
- Familiarity with validation documentation and regulated manufacturing environments