We're looking for a Validation Lead II, working in the Pharmaceuticals & Medical Products industry in Bridgewater, New Jersey, United States.
Creates and maintains all system-related documentation to support the ACES Medical 2012 Project October release. The scope of this documentation includes - User and Functional Requirements Specifications, System Design Specifications, Requirements Traceability Matrices, Operational Qualification test cases, Process Qualification test cases and system training materials.
Manages system documentation review, storage, versioning and signature collection.
Interacts with end users to gather business requirements and information and transcribe them into validation requirements. Responsible for analyzing different use cases and developing requirements.
The pay range we are offering is 72 to 88 per hour. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
3-6 years of experience
Must have very good analytical skills to analyze requirements to develop both positive and negative testing scenarios. Perform Good Documentation Practices review of all test cases post execution.
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.