Scientist I, Analytical Development

BioSpace; Boca Raton (FL); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

401K plan with employer match

Medical, Vision, Life and Dental

Pet Insurance

Company paid STD and LTD

Company Paid Holidays

3 Weeks’ Paid Time Off

Tuition Assistance

Free shuttle to Boca Tri-Rail

Job summary

ADMA Biologics in Boca Raton, FL is seeking a Scientist I, Analytical Development to advance analytical methods for protein quantification and characterization. The role emphasizes development, validation, transfer of assays, and cross-functional collaboration within a cGMP framework.

The candidate will design analytical studies, perform experiments, and generate data for validation projects, with emphasis on ELISA, chromatography, and spectrophotometric techniques.

Qualifications

• BS required in Biological Sciences, Chemistry, Biochemistry or related field.
• MS or PhD preferred.
• 4 years lab experience with BS; 2 years with MS; regulated environment experience required.

Responsibilities

• Develop, validate/qualify, and transfer analytical methods and bioassays (ELISA, chromatographic, spectrophotometric).
• Plan and execute studies to support protein characterization and quantification.
• Conduct experiments to generate data for validations and other projects.
• Interpret data using Excel and other tools; prepare technical reports.

Skills

ELISA

Chromatography

Spectrophotometry

Data analysis

SOPs

cGMP

Education

BS in Biological Sciences

MS in Biological Sciences

PhD in Biological Sciences

Job description

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

• 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.