Scientist I, Analytical Development

Remote: 
Full Remote
Contract: 
Work from: 
United States

Offer summary

Qualifications:

Bachelor's degree in Biological Sciences, Chemistry, or Biochemistry; MS or PhD preferred., Minimum of 4 years of laboratory experience with a BS, or 2 years with an MS., Experience in chemical or biochemical testing within regulated environments., Knowledge of FDA, cGMP requirements, and experience with analytical techniques like ELISA, chromatography, and spectrophotometry..

Key responsibilities:

  • Develop, validate, and transfer analytical methods for protein characterization.
  • Perform experiments to support process development and validation projects.
  • Collaborate with cross-functional teams to select and qualify reference standards.
  • Ensure compliance with SOPs, cGMP, and regulatory guidelines while maintaining accurate documentation.

ADMA Biologics, Inc. logo
ADMA Biologics, Inc. Biotech: Biology + Technology SME https://www.admabiologics.com/
501 - 1000 Employees
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Job description

Job Details
Level:    Experienced
Job Location:    ADMA Biologics FL - Boca Raton, FL
Position Type:    Full Time
Education Level:    4 Year Degree
Salary Range:    Undisclosed
Job Category:    Pharmaceutical
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.

 

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.  

Qualifications

  • 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:

  • 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.

 

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
  • Company paid 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.

Required profile

Experience

Industry :
Biotech: Biology + Technology
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Report Writing
  • Time Management
  • Collaboration
  • Problem Solving

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