Degree in the Sciences.
3+ years of experience in analytical method development, method validation, and method transfer/verification.
3+ years of experience running HPLC in a laboratory setting, preferably within the pharmaceutical industry.
Familiarity with cGMPs, EU, 21 CFR Part 210, 211, and 820, ISO and ICH guidelines.
Strong background and understanding of USP, EP, and other pharmacopeia.
Experience in either Dissolution testing or Aerosol testing.
Excellent written and verbal communication skills.
Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) or related software.
Ability to read and interpret documents such as standard operating procedures, manuals, experimental protocols, and analytical methods.
Legible handwriting.
Bachelor's Degree in Chemistry or relevant field with a minimum of 3 years of analytical laboratory experience.
Excellent organizational and communication skills.
Ability to communicate clearly in writing and orally, including in the creation of standard operating procedures and work instructions.
Ability to communicate with clients on topics such as method development, data interpretation, and investigations.
Hands-on skilled coordination and dexterity with attention to detail.
Application of basic arithmetic concepts such as addition, subtraction, fractions, percentages, ratios, and proportions to practical solutions.
