Donor Center Medical Professional & Trainer

Octapharma Plasma, Inc.

San Antonio (TX)

On-site

USD 42,000 - 66,000

Full time

2 days ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
HSA
FSA
Tuition reimbursement
EAP
Wellness program
401k
Paid time off
Company holidays
Personal time

Job summary

Octapharma Plasma, Inc. is hiring a Donor Center Professional to evaluate donor eligibility for automated plasmapheresis. The role administers approved immunizations per SOPs and state regulations and provides limited emergency care as permitted by licensure.

You will ensure compliance with cGMP and all regulatory guidelines. Responsibilities include medical history reviews, donor data documentation in NexLynk, monitoring for adverse reactions, and coordination with the center Licensed

Qualifications

  • Graduate of a healthcare-related program (e.g., Physician, RN, LPN).
  • Current CPR certification.
  • Experience in hospital, field care, or plasma center preferred.
  • Must work within the scope of professional license/certification per state rules.

Responsibilities

  • Evaluate donor eligibility via medical history, physicals, and informed consent per SOPs and regulatory guidelines.
  • Review and document donor information, immunization records, and test results in NexLynk.
  • Monitor for adverse donor reactions and provide care as trained.
  • Consult with center physician on abnormal results and eligibility concerns.
  • Maintain documentation and train as Donor Center Technician I; support QA backup and trainer roles.

Skills

Medical knowledge
CPR certification
EMT certification
Nursing license

Education

Healthcare-related education

Tools

NexLynk donor management system

Job description

Octapharma Plasma, Inc. is hiring a Donor Center Professional to evaluate donor eligibility for automated plasmapheresis. The role administers approved immunizations per SOPs and state regulations and provides limited emergency care as permitted by licensure.

You will ensure compliance with cGMP and all regulatory guidelines. Responsibilities include medical history reviews, donor data documentation in NexLynk, monitoring for adverse reactions, and coordination with the center Licensed

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