
Quality Associate
Review and approval of batch related documentation (cGMP procedures, Master Production Records, Solution Lot records, protocols and reports) to support product disposition. Executes activities including; intermediate technical writing, intermediate investigation support (root cause analysis/impact assessment), project representation (moderate complexity). Supports resolution of both technical and compliance issues/gaps of moderate complexity. Aides in implementation of Quality Systems/System Improvements. Control and release of equipment from maintenance, validation, change control and product changeover.
2-4 years directly related to position responsibilities
Quality concepts-able to practice and implement them
Flexible and able to adapt to change
General understanding of manufacturing process, FDA/EMA regulations
Data Analysis
Time Management
Record keeping
Adaptable
Process Improvement
Detail Oriented
Communication Skills
Problem-Solving
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Randstad North America is a wholly-owned subsidiary of Randstad Holding nv, a global provider of HR services. Through its unique approach of delivering HR innovation with human interaction at the center, Randstad secures and manages a workforce of more than 100,000 people for thousands of clients each week. As a trusted partner in the post-digital world of talent, Randstad advances the careers and business success of our candidates and clients.

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