Total Quality Management Director - Hartford

Company: On Time Talent Solutions
Location: Hartford
Posted on: January 8, 2022

Job Description:

Total Quality Management Director - Hartford Title: Total Quality Management Director - Hartford Date Posted: Tuesday, September 7, 2021 Job Type: Permanent City: Hartford State: Connecticut Total Quality Management Director Hartford, Connecticut Hartford is the capital of Connecticut. Hartford was founded in 1635 and is among the oldest cities in the United States. It is home to the country's oldest public art museum (Wadsworth Atheneum), the oldest publicly funded park (Bushnell Park), and the oldest continuously published newspaper (the Hartford Courant). It is also home to the Mark Twain House, where the author wrote his most famous works. Whether you are looking to relocate or are a current resident, job opportunities in Hartford are abundant. On Time Talent Solutions is actively pursuing a Total Quality Manager to be a team leader in providing training, tools, and logistical assistance for quality initiatives. Successful applicants will have a proven track record of developing tools and measuring methods to ensure products and services meet quality standards. Total Quality Management Director Responsibilities: Oversee the development and maintenance of consistent TQM policies, procedures, processes and systems for the TQM department Lead Company Life Sciences services through insights about industry trends and customer needs in the area of Quality Management Systems Ensure that project/department goals are met and adhering to approved budgets Provide advice and support to functional operational teams within the Lifecycle Safety Department including ICSR case processing, regulatory reporting, medical Information, endpoint adjudication and aggregate reporting Track project status, issues, and risks as well as present summary information to clients, partnerships, and executive sponsors as needed Total Quality Management Director Qualifications: Bachelor's degree in life sciences or equivalent nursing qualification with a minimum of 7 years' experience in Lifecycle Safety (Pharmacovigilance, CEVA, Medical Information, Safety Publishing, Risk Management, etc) Sound working knowledge of medical terminology, clinical monitoring procedures (SOPs), ICH-GCP, applicable regulatory requirements, quality management processes Experience with leading QMS platforms such as Trackwise, MasterControl, Pilgrim, Veeva Vault QMS Knowledge of National and International Regulations and Drug Development processes Demonstrated ability to work in a matrix environment

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