QA Specialist
Job in
Appleton, Outagamie County, Wisconsin, 54914, USA
Listed on 2026-02-06
Listing for:
COMMUNITY BLOOD CTR INC
Full Time
position Listed on 2026-02-06
Job specializations:
-
Quality Assurance - QA/QC
-
Healthcare
Job Description & How to Apply Below
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 (other duties may be assigned)- Maintains and recommends improvements to The Community Blood Center’s Quality Plan.
- Reviews and implements SOP’s and training documents related to Quality Assurance processes and systems in order to ensure regulatory compliance.
- Reviews and critiques SOP’s 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, which may include the implementation of new/revised documents, and the 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. Communicates trends to management.
- Reviews equipment and process validation documentation.
- Evaluates deviations and non-conformances reported via the deviation management system and other sources. Determines 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. 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.
- Assures quality service to all customers.
- Complies with all policies and procedures outlined in the CBC Employee Handbook, Center SOP’s, and/or directives. Maintains current level of job-related skills by attending in-services, training sessions, and reading publications.
- Performs all other duties, at the discretion of management, as assigned.
- Bachelor’s degree preferred. Experience in medical technology or a clinical allied health field is 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 is preferred.
- Excellent organizational, oral, and written communication skills.
- Strong analytical and problem-solving skills.
- Skilled 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.
- Health, vision, and dental insurance coverage
- Health Savings Account (HSA)
- PTO/Sick Time
- Paid holidays
- 403(b) retirement savings plan with matching contributions
- Employee Assistance Program
- Discounted YMCA membership
- Disability and life insurance
- Regular employee forums and committees — everyone on our team has a voice!
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