Job Information
Randstad US quality assurance coordinator in scottsdale, Arizona
quality assurance coordinator.
scottsdale , arizona
posted april 15, 2024
job details
summary
$55,000 - $58,000 per year
permanent
high school
category life, physical, and social science occupations
reference47908
job details
job summary:
Randstad is the #1 HR Solutions company in the World and we are sourcing for a Quality Assurance Coordinator in the Scottsdale, AZ area. We are looking for a candidate with solid work experience, great attitude, strong communicator who is looking for a long term opportunity. They must be familiar with working in a regulated environment (Med Device / Pharma). Attention to detail is paramount for this role as they will be managing and organizing all company documents and records. They must also be a strong communicator as they will be collaborating with all levels of the organization. This is a direct hire position and can start immediately.
location: Scottsdale, Arizona
job type: Permanent
salary: $55,000 - 58,000 per year
work hours: 7 to 3
education: High School
responsibilities:
Responsibilities
-The Quality Assurance Coordinator performs ocular and tissue donor record quality assurance review in compliance with org, FDA, EBAA, and AATB policies, procedures, regulations, and standards
-This position facilitates requests from hospitals, medical examiners, coroner's facilities, or other external agencies to ensure complete donor records are obtained
-Receives, compiles, and prepares the donor record for eligibility review and signature of donor records as applicable
-As needed, meets with the Tissue Bank Medical Director(s) to review, and answer questions pertaining to the information and documentation within the donor record
-Facilitates requests from hospital/medical examiner or corner's facility (or other external entities as requested) for data and medical record documentation in accordance with regulatory and accreditation entity requirements as well as internal Policy and procedure
-Receive, compile, and places appropriate documents within the donor records, when necessary, as required by sharing of donor information
-Recognizes and reports trends and opportunities for improvement related to donor records and OPO statistics to the Quality Assurance Manager
-Participates in required quality training and educational growth to ensure staff is competent, compliant, and trained in quality related tasks with all regulatory and accreditation entities and internal standards
-Responsible for supporting the use of systems within the Quality Management System and improvement initiatives within the quality department
-Maintains open verbal and written communication with org and location Quality Department teams and all other applicable departments as it relates to job functions and tasks
-If applicable, answers donor recovery screening questions as needed on an on-call basis on behalf of the organization
-Assists in training and mentoring of new Quality Assurance Coordinators
-Assist in providing initial, periodic and re-training of quality documentation for ocular and tissue donor related activities for quality and recovery staff
-Acts as a role model for Quality Departments by supporting, reinforcing, and exhibiting behaviors consistent with the core values
-Performs other related duties as assigned
qualifications:
Required Qualifications:
Bachelor's degree in business administration, information management, or related field preferred or high school diploma/equivalent with 3 years relevant work experience in a regulated environment (Med Device/Pharma).
Proven experience in quality assurance/quality control, document control, records management, or related roles.
Strong attention to detail and accuracy in document handling and data entry.
Proficiency in document management software and the Microsoft Office suite.
Excellent organizational and time management skills, with the ability to prioritize tasks effectively.
Strong communication and interpersonal skills, facilitating effective collaboration with cross-functional teams.
Knowledge of regulatory requirements and standards related to document control (e.g., ISO 9001, FDA regulations) is advantageous.
Ability to maintain confidentiality and handle sensitive information with discretion.
skills: Quality control, SOP, Quality Assurance, Biology, Chemistry, GMP (Good Manufacturing Practice)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
Applications accepted on ongoing basis until filled.