We're looking for a Senior Regulatory Specialist, working in the Pharmaceuticals & Medical Products industry in Princeton, New Jersey, United States.
Implements and maintains the effectiveness of the quality system.
Supports manufacturing/operations day to day activities for change control.
Provides consultation/advice to regulatory specialist for change control and product development.
Provides regulatory direction/interpretation on team activities.
Interprets and applies regulatory understanding to support of products and teams.
The pay range we're offering is 30 to 35 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
BS preferred in a technical discipline like Biology, Chemistry, Microbiology, Immunology, Medical Technology, etc.
2+ years regulatory experience and/or 2 years relevant industrial experience typically with a quality, product-development/support, or scientific affairs function
Knowledge of regulations and standards affecting IVDs and/or biologics.
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.