Chemist III

Chemist III Boca Raton, FL Job Details Full-time 1 day ago Benefits Paid holidays Disability insurance Health insurance Dental insurance Tuition reimbursement Paid time off Vision insurance 401(k) matching Pet insurance Qualifications EPA Molecular Biology Biochemistry Document review (document control) Procedural guides 5 years Regulatory compliance GMP Laboratory equipment calibration Material testing Bachelor's degree Laboratory compliance Laboratory quality control Laboratory techniques Quality inspection Data entry Quality standards in production Chemistry Bachelor's degree in molecular biology Senior level Cross-functional collaboration Bachelor's degree in biochemistry Communication skills Molecular biology Bachelor's degree in chemistry Cross-functional communication FDA regulations Time management Full Job Description 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 III in Boca Raton, FL!

Job Title:

Chemist III Job Description:

Position Summary:

The Chemist III is responsible for designing, conducting, and implementing quality control testing as well as reviewing documented test results to ensure compliance with specifications and procedures. The Chemist III uses knowledge and creativity to recommend solutions to problems.

Essential Functions and Responsibilities:

Perform quality control testing for raw materials, in-process and final product samples, according to approved Standard Operating Procedures and cGMP guidelines. Complete testing documentation and data entry as required for procedures and test performed. Review and/or approve cGMP documentation generated by other analysts in the laboratory. Accountable for following Standard Operating Procedures (SOPs) and adhering to cGMP guidelines. Perform testing as needed to generate data for validations and other special projects. Perform instrument calibration or qualification according to written procedures. Write and review SOPs and/or Validation Protocols. Use judgment, creativity, and sound technical knowledge to obtain and recommend solutions to problems as directed by QC management. Maintain current knowledge in field of expertise.

Competencies:

Possess time management skills and be able to balance multiple job assignments at once Possesses excellent oral and written communication skills with close attention to detail and accuracy to collaborate effectively with cross-functional teams and communicate findings and recommendations Possesses strong organizational, critical thinking, reasoning, and problem-solving abilities.

Education and Experience Requirements:

Education Requirements :

Bachelor's Degree in Chemistry, Biochemistry, Molecular Biology or related science discipline.

Experience Requirements :

This position requires at least five years of experience in Chemical/Biochemical testing, including experience in a regulated environment (FDA, EPA, etc.). Knowledge of FDA cGMP requirements is an essential pre-requisite for this position.

Compliance Requirements:

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:

In addition to competitive compensation, we offer a comprehensive benefits package including: 401K plan with employer match and immediate vesting Medical, Vision, Life and Dental Insurance Pet Insurance Company paid STD and LTD Company Paid Holidays 3 Weeks' Paid Time Off (within the first year) Tuition Assistance (after the first year) Easily accessible to Tri-Rail Free shuttle to the Boca Tri-Rail station 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 . ADMA Biologics is an Equal Opportunity Employer. Apply now