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ADMA Biologics is seeking a Specialist I, Raw Materials in Boca Raton, FL. The role involves quality control of raw materials, testing, and data entry in a regulated environment.
The position requires a B.S. or A.S. in a related science or equivalent experience, with 0–3 years in a pharmaceutical setting. A strong focus on cGMP and SOP adherence is essential to support compliant operations and QA/government audits.
ADMA 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 Specialist I, Raw Materials in Boca Raton, Florida!
ADMA 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 Specialist I, Raw Materials in Boca Raton, Florida!
Position Summary
The Specialist I, Raw Materials performs quality control raw material processing and testing, following general instructions on routine work and detailed instructions on new assignments.
The minimum compliance expectation for this role entails strict adherence to FDA regulations and company policies governing sales and marketing activities. This includes completion of required compliance training, accurate documentation of sales interactions, and adherence to data privacy regulations. Additionally, the role requires proactive participation in compliance reviews, prompt reporting of any potential issues, and ongoing education to stay updated on relevant FDA regulations.
In addition to competitive compensation, we offer a comprehensive benefits package including:
ADMA Biologics is an Equal Opportunity Employer.