Total Quality Management Director - Indianapolis


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Total Quality Management Director

Indianapolis, Indiana

 

As the state capital, Indianapolis is the most populous city in Indiana. Downtown Indianapolis boasts the largest employment cluster in Indiana, with nearly 43,000 jobs per square mile. With a low unemployment rate in Marion County, Indianapolis is a great area for talented healthcare professionals to live. Whether you prefer to work in a hospital, clinic, home care or senior housing setting—Greater Indianapolis job opportunities in healthcare 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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