cGMP‑Driven MV Documentation Specialist
Y-Axis
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. #J-18808-Ljbffr Y-Axis
Vacancy posted 1 day ago
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