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ADMA Biologics, Hammond, LA is seeking a Physician Substitute – LPN, RN, Paramedic or EMT-A to assist the Medical Director and center physicians with donor screening, phlebotomy and medical oversight. The role performs donor physicals, manages consent processes, reviews lab results and ensures cGMP compliance while maintaining accurate donor records.
CPR certification and active RN/LPN/EMT licenses are required.
Job Description Header
Physician Substitute - LPN, RN, Paramedic or EMT-A in Hammond, LA! Job Title: Physician Substitute - LPN, RN, Paramedic or EMT-A
Job Description HeaderADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Physician Substitute - LPN, RN, Paramedic or EMT-A in Hammond, LA! Job Title: Physician Substitute - LPN, RN, Paramedic or EMT-A
Position Summary
Under the direction of the Medical Director and/or Center Licensed Physician(s), the Physician Substitute determines the acceptability of all first-time donors and return applicant donors. The Physician Substitute determines the suitability of donors by following Standard Operating Procedures (SOPs) designed to ensure the donor meets suitability criteria in accordance with FDA guidance and regulations. The Physician Substitute also reviews normal donor laboratory test and refers abnormal test to the Physician for review.
The Physician Substitute works closely with the Medical Director or Licensed Center Physician(s) while making any decisions which directly impact donor suitability. The Physician Substitute also provides medical oversight in screening, phlebotomy, and the plasma processing areas.
Competencies
Ability to follow the cGMP’s and procedures with great attention to detail
Able to work in high-pressure, deadline-driven environment
Basic computer skills including experience with software programs such as Word, Excel, and GroupWise
Demonstrated ability to achieve goals, overcome obstacles, and meet deadlines
Demonstrated ability to work well with people from diverse backgrounds
Maintains a professional appearance and demeanor when interacting with peers and donors
As a part of our Quality Systems and cGMP initiatives, employees are responsible for ensuring compliance with all ADMA Quality policies, standards, and SOPs in their area of work and responsibility. This includes ensuring all Quality Assurance (QA) records and reports, Human Resources (HR) policies, and Environmental Health and Safety (EH&S) procedures and practices are completed in a timely manner. Any delay or failure to comply with policies, standards and procedures is required to be communicated/escalated to the appropriate responsible parties, such as QA, HR, or EH&S depending on the issue.
ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify.