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Regulatory Compliance Specialist

Catalyst Life Sciences
Cranbury, NJ Full Time
POSTED ON 4/7/2025
AVAILABLE BEFORE 5/7/2025

Catalyst Life Sciences seeks a dedicated QC Stability Program Manager to oversee the analytical testing and validation processes in our growing team.

The ideal candidate will have at least 6 years of QC lab experience in an FDA regulated environment, preferably within the pharmaceutical industry. They should also possess strong management and project management skills.

We are looking for someone who can effectively manage and oversee the analytical testing and validation processes, ensuring compliance with regulatory requirements. If you are a detail-oriented professional with excellent communication skills, we encourage you to apply.

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