Associate Validation & Qualification

About the role

Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Whether you are engaged in development, maintenance, compliance, or analysis through research programs, your contribution will have a direct impact on patients.

What you'll do

• Support Technology Transfer activities , including execution of laboratory, scale-up, exhibit, and validation batches
• Prepare and review study protocols, technical assessments, and scientific reports to support process understanding and product readiness
• Support preparation and review of technical documentation and responses for regulatory submissions and deliverables
• Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with regulatory requirements and company policies
• Troubleshoot validation problems for equipment and performance processes, conducting statistical analysis of testing results to address process anomalies

What you need

• 6–11 yrs of experience
• GMP
• Regulatory affairs
• Documentation
• Medication administration
• Technical writing
• Calibration
• Diploma