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QA Specialist

Job in Appleton, Outagamie County, Wisconsin, 54914, USA
Listing for: The Community Blood Center
Full Time position
Listed on 2026-01-28
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Job Requirements

Do you like working behind-the-scenes, but want a job that impacts people in your community? Then consider becoming a Quality Assurance Specialist at The Community Blood Center. By joining our team, you’ll play a critical role in this life-saving mission.

Job Summary

The Quality Assurance Specialist is a full-time position responsible for ensuring compliance with regulatory, accreditation, certification, CBC, and customer requirements. This role supports the implementation of effective manufacturing processes and system controls to promote continuous product safety and quality. The specialist ensures current Good Manufacturing Practices (cGMPs) are adhered to and integrated across all organizational systems.

ESSENTIAL DUTIES AND RESPONSIBILITIES
  • Maintains and recommends improvements to The Community Blood Center’s Quality Plan.
  • Reviews and implements SOPs and training documents related to Quality Assurance processes and systems to ensure regulatory compliance.
  • Reviews and critiques SOPs and training documents submitted from department management for adherence to current FDA, AABB, and other regulatory guidelines.
  • Provides training and education regarding quality, cGMP, and safety for the organization.
  • Manages the change control process for policies, processes and procedures, including implementation of new/revised documents and archiving of old documents.
  • Assists users of quality management software in analysis and reporting of data.
  • Participates in quality improvement and corrective action teams within and across operational areas.
  • Reviews data from quality management software and other sources to identify trends and communicates trends to management.
  • Reviews equipment and process validation documentation.
  • Evaluates deviations and non-conformances reported via the deviation management system and other sources to determine if immediate correction is appropriate or should be evaluated for corrective action.
  • Escalates to management errors requiring further evaluation and/or submission of reports to FDA.
  • Participates in the tracking, monitoring, and reporting of quality indicators and performs trend analysis to monitor process and facility performance.
  • Develops audit plans, conducts quality audits, prepares audit reports and communicates findings, including compliance risk.
  • Assists with external inspections as needed and assures quality service to all customers.
  • Complies with all policies and procedures outlined in the CBC Employee Handbook, Center SOPs, and/or directives, maintains current level of job-related skills by attending in-services, training sessions, and reading publications, and performs all other duties at the discretion of management as assigned.
Experience and Qualifications
  • Bachelor’s degree preferred.
  • Experience in medical technology or a clinical allied health field preferred.
  • 1-3 years of experience in a blood center, biologics, pharmaceutical or medical industry manufacturing environment with base familiarity of quality assurance practices, training, and federal regulatory practices preferred.
  • Excellent organizational, oral, and written communication skills.
  • Strong analytical and problem-solving skills.
  • Strong flexible interpersonal skills and skill in observation of operational tasks.
  • Skilled in documentation review with special emphasis on details.
  • Computer skills with emphasis on word processing and database software; employee may occasionally be required to lift objects or materials weighing up to 25 pounds.
Application Instructions

Apply Online: https://(Use the "Apply for this Job" box below)./

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