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Analytical Chemist
Actalent
An engineering and sciences services and talent solutions firm connecting specialized experts with industry projects.
Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.
Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.
Evaluate test results and determine the acceptability of samples based on the results.
Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs.
Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.
Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.
Review notebooks promptly and ensure compliance with SOPs.
Analyze and interpret results in both written and oral formats.
What you bring
fda
gmp
instrumentation
hplc
uv-vis
bachelor’s
Familiarity with FDA and GMP regulations.
Working knowledge of instrumentation software used in laboratories.
Ability to analyze and interpret complex data.
Proficiency in HPLC, UPLC, and UV-Vis techniques.
Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience.
Benefits
Time Off/Leave (PTO, Vacation or Sick Leave)
Health Spending Account (HSA)
Employee Assistance Program
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Transportation benefits
Critical Illness, Accident, and Hospital
Medical, dental & vision
Short and long-term disability
401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
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