Fda Regulations Jobs in Richardson, TX

PRIMARY RESPONSIBILITIESCollects tracks and submits exam deliverables to regulators and banking partnersCreates project plans as they relate to audit and exam remediationsAssesses exam and audit deliverables for adequacy and completenessProvides compliance support services to Board of More...

The Associate Director Immunology Field Training Dermatology is responsible for the team developing the sales franchise curriculum for AbbVie field personnel and field management. This person will create lead and work within crossfunctional teams made of participants from Training Me More...

Mavenir is building the future of networks and pioneering advanced technology focusing on the vision of a single softwarebased automated network that runs on any cloud. As the industrys only endtoend cloudnative network software provider Mavenir is transforming the way the world conne More...

The Senior Manager Regulatory Affairs US Advertising and Promotion ImmunologyDermatology combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet the required legislation. Additionally the individual deve More...

Responsibilities: Candidate must be able to answer questions in the STAR format (Situation Task Action Result). If they cannot formulate a response this way please coach or whittle down the resume. Note answers should pull from multiple projects and not the same one over and over. C More...

The Senior Director of Regulatory Affairs ensures that all divisions comply with applicable federal state and provincial laws and regulations maintaining continuous operating approvals. This role also leads efforts to develop and influence regulatory policies impacting the delivery of More...

The Jr. Clinical Investigator CRS oversees the clinical research of consumer products involving healthy paid volunteers. Develops research studies and creates standards and guidelines for clinical research services and programs. Ensures adherence to standard operating procedures good More...

The Manager Regulatory Affairs US Advertising & Promotion combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet required legislation. The Manager has the responsibility for 12 of the following: the More...

As a leading pharmaceutical company AbbVie is constantly striving to discover and deliver innovative medicines and solutions that address complex health issues and enhance peoples lives. Bringing a new drug to patients is a complex process that involves not only scientific research an More...

The Associate Director Market Access Field Training has primary responsibility to partner with Leaders across AbbVies portfolio of businesses to help diagnose needs and develop solutions that support skill development across market access competencies to create a world class Market Ac More...

Why We Work at Dun & BradstreetDun & Bradstreet unlocks the power of data through analytics creating a better tomorrow. Each day we are finding new ways to strengthen our awardwinning culture and accelerate creativity innovation and growth. Our 6000 global team members are pas More...

Why We Work at Dun & BradstreetDun & Bradstreet unlocks the power of data through analytics creating a better tomorrow. Each day we are finding new ways to strengthen our awardwinning culture and accelerate creativity innovation and growth. Our 6000 global team members are pas More...

Why We Work at Dun & BradstreetDun & Bradstreet unlocks the power of data through analytics creating a better tomorrow. Each day we are finding new ways to strengthen our awardwinning culture and accelerate creativity innovation and growth. Our 6000 global team members are pas More...

Responsibilities: Lead the validation team in a strategic riskbased approach that optimizes legacy Computer System documentation CSA strategies and strong SAP ECC>S/4 HANAconversion knowledge to successfully deliver a validated system meeting all project requirements. Review approva More...

You will be responsible for the development and implementation of a seamless and engaging onboarding and acclimation strategy that aligns new hires to the company vision culture and expectations to equip them for success. The successful candidate will be innovative operate with a sens More...

*Employee can work remotely anywhere in the U.S.  The Principal Medical Writer is responsible for providing writing support and advanced scientific writing expertise to the teams ensuring successful preparation of high quality documents and effective implementation of the wr More...

*Employee can work remotely anywhere in the U.S. The Senior Medical Writer is responsible for providing medical writing ensuring successful preparation of high quality documents and effective implementation of the writing process. Provides medical writing expertise for multiple c More...

*Employee can work remotely anywhere in the U.S. The Senior Medical Writer is responsible for providing medical writing ensuring successful preparation of high quality documents and effective implementation of the writing process. Provides medical writing expertise for multiple c More...

*Employee can work remotely anywhere in the U.S.  The Principal Medical Writer is responsible for providing writing support and advanced scientific writing expertise to the teams ensuring successful preparation of high quality documents and effective implementation of the wr More...

Roles & Responsibilities: Full lifecycle validation for all applicable computerized systems ensuring they are designed validated operated and retired in compliance with GxP regulation and computer system validation (CSV) guidance. Compiling and maintaining accurate CSV documentation More...