Summary: A global pharma leader is currently seeking a detail-oriented Supervisor to join their Massachusetts site. As part of the cell and gene therapy department, you will oversee a team to ensure the cGMP compliance of flow cytometry methods.
Responsibilities:
- Performing method development and validation activities as per cGMP requirements
- Writing, reviewing, and following SOPs
- Providing analytical support for manufacturing operations
- Identifying, reporting, and monitoring laboratory discrepancies
Qualifications:
- Bachelor's degree, preferably Master's/PhD
- 4+ years of Life Sciences industry experience
- Extensive knowledge of cGMP standards
- Authored SOPs
If you're interested in this Supervisor role, then please don't wait to apply!
