Documentation Specialist I

Apply now and our proprietary system will quickly have you in front of a live recruiter. The Opportunity Description We're looking for a Documentation Specialist I , working in Pharmaceuticals and Medical Products industry in 1000 Research Parkway, Meriden, Connecticut, 06450, United States . Job description: Organizes and reviews change control and other GMP documentation. Assists with the editing of quality documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulator requirements. Archives and organizes GMP documents as well as review of logbooks and temperature monitoring charts to ensure adherance to SOPs and specifications. Activates GMP documents such as batch records and SOPs will be an additional assigned task. Other documentation duties as assigned. 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: Must be proficient in Microsoft Word and Excel Must possess sound interpersonal and information gathering skills Able to relate well to others at all levels throughout the organization Ability to work in a team environment, effectively interacting with others 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?