3rd Shift Lab Technician: GMP/QA & Compliance

BioLife Plasma; Hoover (AL); On-site; USD 26,000 - 41,000; Full time

Job summary

BioLife Plasma Services in Hoover, AL seeks a Lab Technician for 3rd shift to perform high and moderate complexity testing per SOPs, ensure accurate donor results, and maintain quality control records. You will support sample handling, calibrations, and documentation while adhering to GMP/CLIA standards and participating in process improvements.

The role requires a biomedical degree, SOP literacy, and strong attention to quality, with excellent communication and problem-solving abilities.

Qualifications

• Bachelor’s degree from an accredited college in a biomedical discipline, such as chemical, physical, biological, clinical laboratory science, or medical technology.
• Ability to read, follow, and apply SOPs and maintain complete and accurate records.
• Strong attention to detail and commitment to quality, compliance, and data integrity.
• Excellent written and verbal communication, interpersonal, and analytical/problem-solving skills.
• Proficiency using PCs and applicable software.

Responsibilities

• Perform authorized high and moderate complexity laboratory testing per SOPs and regulations.
• Support sample management, test performance, quality control, result review and reporting.
• Maintain records of donor test results and instrument calibrations.
• Identify issues affecting test performance and notify management as needed.
• Participate in continuous improvement initiatives (5S, Kaizen).

Skills

Attention to detail

Written communication

Verbal communication

Interpersonal skills

Analytical/problem solving

Education

Bachelor’s degree in biomedical disciplines

MT/MLT certification (ASCP)

Job description

BioLife Plasma Services in Hoover, AL seeks a Lab Technician for 3rd shift to perform high and moderate complexity testing per SOPs, ensure accurate donor results, and maintain quality control records. You will support sample handling, calibrations, and documentation while adhering to GMP/CLIA standards and participating in process improvements.

The role requires a biomedical degree, SOP literacy, and strong attention to quality, with excellent communication and problem-solving abilities.