The Opportunity

We're looking for a Validation Specialist I, working in the Pharmaceuticals & Medical Products industry in Bridgewater, New Jersey, United States.

Job description:
  • 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.
  • Analyzes different use cases and developing requirements, establishing testing strategy, create UAT plan, develop scripts, execute scripts and write UAT summary report. 
Details

The pay range we are offering is 30 to 40 per hour. This position may present an opportunity to go permanent.

Our Client

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
Requirements:
  • 3-6 years of experience
  • Bachelors degree
  • Validation and PUMA methodology
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.

Not exactly? Join Our Talent Community, and we'll let you know of additional opportunities.

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