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 Chemist I in Boca Raton, Florida!
Job Title: Chemist I
Job Description:

POSITION SUMMARY

The Chemist I will perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments.

EDUCATION REQUIREMENTS:

B.S. in Chemistry, Biochemistry, Molecular Biology or related science discipline is required.

EXPERIENCE REQUIREMENTS:

This position requires experience in a laboratory setting. Work experience in a regulated environment (FDA, EPA, etc.) is preferred.

COMPLIANCE REQUIREMENTS (ES)

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.
Job Description Footer:

ESSENTIAL FUNCTIONS (ES) AND RESPONSIBILITIES

• Perform quality control chemistry and/or Immunoassays for raw materials, in-process and final products according to approved Standard Operating Procedures (SOPs).
• Perform instrument calibration or qualification according to written procedures.
• Perform testing as needed to generate data for method validations and other special projects, following general instructions on routine work and detailed instructions on new assignments.
• Fulfill requests from management for assistance in other matters as needed.
• Accountable for following Standard Operating Procedures (SOPs) and adhering to cGMP guidelines.
• Utilize cGMP practices in documentation and execution of job functions.
• Review documentation on trained tasks as assigned by manager.