JOB REQUIREMENTS: Quality Assurance Professional Job Locations
US-WI-Milwaukee \| US-IL-Aurora \| US-IN-Indianapolis \| US-MI-Grand
Rapids ID 2024-9884 Category Quality Position Type Full Time Overview
Versiti is a fusion of donors, scientific curiosity, and precision
medicine that recognize the gifts of blood and life are precious. We are
home to the world-renowned Blood Research Institute, we enable life
saving gifts from our donors, and provide the science behind the
medicine through our diagnostic laboratories. Versiti brings together
outstanding minds with unparalleled experience in transfusion medicine,
transplantation, stem cells and cellular therapies, oncology and
genomics, diagnostic lab services, and medical and scientific expertise.
This combination of skill and knowledge results in improved patient
outcomes, higher quality services and reduced cost of care for
hospitals, blood centers, hospital systems, research and educational
institutions, and other health care providers. At Versiti, we are
passionate about improving the lives of patients and helping our
healthcare partners thrive. Position Summary This role provides support
to the Quality department in the area(s) of quality, compliance and/or
regulatory affairs. This role supports the overall quality program and
serves as a liaison between the Quality team and other service lines of
Versiti. He/she/they partners with service lines to provide quality
input on projects and everyday tasks. Responsibilities Core Quality
Assurance Specialist Responsibilities * Supports Supervisor/Manager in
executing the Quality Plan and ensuring compliance with applicable
regulations and standards. * Identify and develop quality system
improvements. * May integrate continuous improvement practices adopted
by Versiti into quality systems, education, and improvement activities.
* May support internal/external assessments as assigned and facilitates
optimal communication between the department and the
inspector/assessors. * Prepares charts, tables, etc. to analyze quality
metrics. May communicate results and actions of quality metrics. * May
review, approve and/or execute validation plans, corrective action plans
associated with events, and other required documents for compliance as
required. * Supports operations with review of proposed changes in
methods, manufacturing, or instrumentation. * May support with the
development, compilation, and submission of regulatory submissions as
required. * Review, analyze, approve, and monitor events logged in
event management system, including adequacy of investigation,... For
full info follow application link. We embrace and encourage diversity in
our workforce. Equal Opportunity Employer of Minorities, Females,
Protected Veterans, and Individuals with Disabilities. We participate in
eVerify. We maintain a drug-free workplace and perform pre-employment
substance abuse testing. We are a tobacco/smoke-free workplace.
***** APPLICATION INSTRUCTIONS: Apply Online:
ipc.us/t/533BDF6FAB224B87 Qualified females, minorities, and special
disabled veterans and other veterans are encouraged to apply.