Scientist II, Analytical Development
Company: ADMA Biologics
Location: Boca Raton
Posted on: November 1, 2025
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Job Description:
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 II, Analytical
Development located in Boca Raton, FL! Job Title: Scientist II,
Analytical Development Job Description: Position Summary The
Scientist II, Analytical Development demonstrates success in
technical proficiency, scientific creativity, collaboration with
others and independent thought. Works on complex problems in which
analysis of data requires evaluation of identifiable factors.
Exercises judgment within generally defined practices and policies
in selecting methods and techniques for obtaining solutions.
Essential Functions (ES) and Responsibilities Develop, qualify,
validate analytical and bioanalytical test methods and assays with
minimum supervision, write SOPs and transfer methods to QC
department as needed. Be familiar with regulatory guidelines
pertaining to assay development/qualification/validation and
support regulatory submissions. Design experiments and write
protocols for assay qualification and development. Perform assays
or supervise other analysts for assay qualification and validation
work. Frequently write technical reports and present findings
internally to management or to external clients. Analyze
experimental data with appropriate statistical tools and report
scientific results. Interpret data and adhere to strict guidelines
on documentation when recording data. Review and/or approve cGMP
documentation generated by other analysts in the laboratory if
necessary. Analyze samples from various sources to provide
information on compounds or quantities of compounds present. Use
analytical techniques and instrumentation, such as gas and
high-performance liquid chromatography (HPLC), ion chromatography,
spectroscopy (infrared and ultraviolet amongst others), ELISA, and
potentiometry. Use a range of analytical techniques,
instrumentation and software and serve as a subject matter expert.
Develop new techniques for the analysis of drug products and
chemicals. Use judgment, creativity and sound technical knowledge
to obtain and recommend solutions to problems as directed by AD
management. Constantly observe current QC methods and propose areas
for improvement. Perform risk and gap assessment and life cycle of
the existing methods/systems in support of FDA’s requirement for
continuous improvement. Propose efficiencies to existing processes
and be familiar with laboratory automation. Job Responsibilities or
Job Requirements Competencies Ability to follow the cGMP’s and
procedures with great attention to detailAble to work in
high-pressure, deadline-driven environmentDemonstrated ability to
achieve goals, overcome obstacles, and meet deadlinesPossess time
management skills and be able to balance multiple job assignments
at oncePossesses excellent oral and written communication skills
with close attention to detail and accuracy to collaborate
effectively with cross-functional teams and communicate findings
and recommendationsExperience Requirements Education Requirements:
A minimum of a Master's degree in a scientific discipline such as
Chemistry, Analytical Chemistry, Biochemistry, Biological Sciences,
Engineering or equivalent is required. Experience Requirements: A
minimum of five years of related employment experience is required
with a Master's degree. Three years of experience (may include
post-doctoral experience) is required for a PhD. Expert knowledge
of scientific principles and concepts is required. Preferred
Experience 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: 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.
Keywords: ADMA Biologics, Boca Raton , Scientist II, Analytical Development, Science, Research & Development , Boca Raton, Florida
