Description

You will perform stability testing and data analysis within a pharmaceutical environment.

This role is on-site.

Responsibilities

• Execute stability studies in compliance with GMP standards.
• Conduct gap analysis to identify and address procedural or data inconsistencies.
• Utilize LIMS for managing samples and recording analytical results.
• Maintain documentation according to CTD requirements.

Required Skills

• 5+ years of experience in a stability or analytical role.
• Proficiency with GMP regulations.
• Hands-on experience with LIMS.
• Knowledge of CTD documentation structures.
• Experience performing Gap Analysis.
• Background in Microbiology.

Preferred Skills

• Bachelor's degree or higher in any field.

Key Skills

Education

ANY GRADUATE