Description

You will perform manufacturing and quality tasks within a pharmaceutical environment in Pearl River, NY.

Responsibilities

• Execute media preparation processes according to established protocols.
• Operate and maintain bioreactors within a GMP-regulated environment.
• Perform tasks within cold room settings as required by production needs.
• Engage in cross-training to support various manufacturing and quality functions.

Required Skills

• 4+ years of experience in a manufacturing or quality role.
• Direct experience with bioreactor operations.
• Proficiency in media preparation.
• Working knowledge of GMP standards.
• Ability to work in cold room environments.
• Strong interpersonal skills for team collaboration.
• Degree completion (any graduate).

Key Skills

Education

ANY GRADUATE