Manufacturing Specialist
Company: VirtualVocations
Location: New Orleans
Posted on: November 1, 2024
|
|
|
Job Description:
A company is looking for a Specialist Manufacturing with
extensive GMP experience in drug substance manufacturing.
Key Responsibilities
Oversee and manage NC Class II/III records, CAPA, and change
control records
Monitor site performance metrics and identify improvement
opportunities
Coordinate project activities, including meeting minutes and data
analysis
Qualifications & Requirements
5+ years of experience in protein, API, DS, DP, or packaging
manufacturing environments
5+ years of knowledge in cGMP principles and FDA regulatory
guidelines
Experience managing quality records and validation principles
Strong team leadership and facilitation skills
Preferred scientific degree or equivalent practical experience in
GMP environments
Keywords: VirtualVocations, Gulf Port , Manufacturing Specialist, Other , New Orleans, Mississippi
|
Click
here to apply!
|
