Tris Pharma, Inc. is seeking a Method Validation Documentation Specialist to support the MV department by creating, revising and organizing specifications and test methods under the MOC system in line with cGMP standards.
The role requires a chemistry-focused education with extensive experience in analytical development or MV, proficiency with multiple analytical instruments, and strong documentation and regulatory compliance skills for submission support.
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cGMP‑Driven MV Documentation Specialist
Y-Axis · Franklin Park, NJ, USA ·
- Pay:
- 80.000 - 100.000
- Job type:
- Full Time