QA Associate: Healthcare Compliance & Records

Central-California-Blood-Center

Fresno (CA)

On-site

USD 29,000 - 35,000

Full time

14 days+

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Job summary

Central California Blood Center is seeking a QA-support professional to assist the Quality Assurance Department in maintaining policies, procedures, and regulatory timelines. The role requires strong written and verbal communication, confidentiality, and proficient computer skills, with on-site duties at the Fresno location.

Responsibilities include document control, reporting for FDA deviations, and aiding in license renewals while aligning with the company’s standards and values.

Qualifications

  • High School Diploma or GED required.
  • 1–3 years working in a healthcare field or blood banking preferred or equivalent.
  • Strong writing and proofreading skills.
  • Proficient in Microsoft Office, especially Excel.
  • Knowledge of federal regulatory/state requirements and accreditation standards preferred.

Responsibilities

  • Organize, reconcile, review, route and maintain department documents and records.
  • Maintain off-site storage including lists and files, coordinate retrievals.
  • Assist with gathering information for Post Donation Information (PDI) reports and QIRs.
  • Prepare reporting materials for FDA deviations and notifications within established timeframes.
  • Provide routine office support and prepare correspondence.
  • Maintain QA calendars and assist with license renewals and audits.

Skills

Writing skills
Customer service
Healthcare terminology
MS Office proficiency
Regulatory knowledge
Time management

Education

High School Diploma or GED

Tools

Microsoft Office
Excel

Job description

Central California Blood Center is seeking a QA-support professional to assist the Quality Assurance Department in maintaining policies, procedures, and regulatory timelines. The role requires strong written and verbal communication, confidentiality, and proficient computer skills, with on-site duties at the Fresno location.

Responsibilities include document control, reporting for FDA deviations, and aiding in license renewals while aligning with the company’s standards and values.

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