What are the responsibilities and job description for the Pharmaceutical Materials Manager position at Catalyst Life Sciences?
QC Stability Program Manager
We are seeking a highly skilled QC Stability Program Manager to oversee analytical testing and validation processes in an FDA regulated environment.
Key Responsibilities:
- Manage and oversee quality control laboratory operations
- Develop and implement stability programs to ensure product safety and efficacy
- Collaborate with cross-functional teams to drive process improvements and optimize laboratory efficiency
Requirements:
- 6 years of experience in a QC lab setting, preferably in the pharmaceutical industry
- Proven track record of managing and leading teams in an FDA regulated environment
- Strong understanding of analytical testing and validation processes
