Scientist I, Analytical Development Employer ADMA Biologics Location Boca Raton, FL Start date Aug 23, 2026 View more categories View less categories Discipline Information Technology , Business/Data Analytics , Science/R D , Biotechnology Required Education Bachelors Degree Position Type Full time Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details Company Job Details 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 Scientist I, Analytical Development in Boca Raton, Florida!

Job Title:

Scientist I, Analytical Development Job Description:

Position Summary:

The Scientist I, Analytical Development demonstrates success in technical proficiency, scientific creativity, collaboration with others and independent thought. As a key member of the Analytical Development group provide analytical support for process development group and manufacturing. Be responsible for the development, implementation and execution of routine analytical techniques for protein quantification and characterization.

Essential Functions and Responsibilities:

Development, optimization, validation/qualification, and tech transfer of analytical test methods and bioanalytical assays such as ELISA, spectrophotometric, chromatographic, gel-based, enzymatic activity and chromogenic assays. Design, development, and hands-on execution of analytical studies to support protein characterization and quantitation. Perform experiments as needed to generate data for validations and other special projects. Evaluate and interpret test and experimental data generated from development/qualification and validation work using Excel or other software as required. Collaborate cross-functionality with other departments to select, qualify, and implement reference standards. Execute assigned tasks within the constraints of timelines, under minimal supervision by senior scientific staff. Troubleshoots technical procedures, methodology and instrumentation. Perform instrument calibration or qualification according to written procedures. Serve as primary authors, reviewers, and approvers of regulated documents such as method validation/qualification reports, protocols, transfers, SOPs, change controls, investigational reports, and deviations. Experience in writing technical reports and presenting findings to internal or external clients. Review and/or approve cGMP documentation generated by other analysts in the laboratory if necessary. Accountable for following Standard Operating Procedures (SOPs), adhering to cGMP guidelines and all relevant compliance regulations. Use judgment, creativity, and sound technical knowledge to obtain and recommend solutions to problems as directed by AD management. Maintain current knowledge in field of expertise and develop subject matter expertise with analytical technology.

Education & Experience Requirements:

Education:

Bachelor of Science (BS) in Biological Sciences, Chemistry, Biochemistry or a relevant discipline is required. Master of Science (MS) in Biological Sciences, Chemistry, Biochemistry or a relevant discipline is preferred. PhD in Biological Sciences, Chemistry, Biochemistry or a relevant discipline is preferred.

Experience:

A minimum of 4 years of related lab experience with a BS is required. A minimum of 2 years of related lab experience with a MS is required. Experience in Chemical/Biochemical testing is required. Experience in a regulated environment (FDA, EPA, etc.) is required. Knowledge of FDA and cGMP requirements are required.

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. Company ADMA Biologics is an end-to-end commercial biopharmaceutical company committed to manufacturing, marketing and developing specialty plasma-derived products for the prevention and treatment of infectious diseases in the immune compromised and other patients at risk for infection. Our devotion to these underserved populations fuels us, and our hands-on approach to production and development sets us apart.

Company info Website http:

//www.admabiologics.com/ Phone 201-478-5222 Location 5800 Park of Commerce Blvd. NW Boca Raton, FL 33487 United States Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert Similar jobs Process Development Sr Scientist Thousand Oaks, California Principal Research Scientist II, Molecular Profiling and Drug Delivery (MPDD) North Chicago, IL Sr. Assoc. Scientist Hawthorne, New York