Blood Products Technician I - Night Shift

Community Blood Center of Greater Kansas City; Kansas City (MO); On-site; USD 38,000 - 52,000; Full time

Job summary

Community Blood Center of Greater Kansas City is seeking a Blood Product Processor to prepare and label products per SOPs, inspect quality at each step, and maintain accurate records. The role requires attention to detail, ability to work independently, and strong teamwork in a regulated environment.

Responsibilities include equipment maintenance, data entry in BECS, and generating reports while ensuring compliance with FDA, AABB, and cGMP standards.

Qualifications

• High school education or equivalent.
• No prior work experience required.
• Familiar with AABB, FDA, OSHA regulations.
• Proficient in BECS and Microsoft Office.

Responsibilities

• Prepare and label products according to SOPs.
• Perform visual inspection of blood products.
• Maintain accurate records.
• Perform equipment maintenance and quality control.
• Identify and report problems that may affect products.
• Quarantine products or supplies when required.
• Unpack, receive, and inspect shipments.
• Prepare shipments of donor samples, plasma, and recovered plasma.
• Respond to environmental and storage alarms and take corrective action.
• Data entry into BECS and use of related software.
• Generate various reports as needed.

Skills

Attention to detail

Cultural competency

Reliability

Strong work ethic

Independence

Clear communication

Team player

Organizational skills

Multitasking

Attendance adherence

Problem reporting

Education

High school education or equivalent

Tools

BECS

Microsoft Suites

Job description

Community Blood Center of Greater Kansas City is seeking a Blood Product Processor to prepare and label products per SOPs, inspect quality at each step, and maintain accurate records. The role requires attention to detail, ability to work independently, and strong teamwork in a regulated environment.

Responsibilities include equipment maintenance, data entry in BECS, and generating reports while ensuring compliance with FDA, AABB, and cGMP standards.