Shape pharmaceutical quality through analytical method validation and stability studies as a Senior Scientist in hybrid Kimberley, Northern Cape, ZA. Use chromatography to assess products and intermediates.
This Senior Analytical Development Scientist supports pharmaceutical development across identification, quantification, purity, and shelf-life assessment. Core expertise includes HPLC, UPLC, LC-MS, data analysis, and LIMS. The position requires technical documentation, regulatory awareness, and collaboration across scientific and quality teams.
Key Responsibilities:
Assess drug substance and product identity, purity, and quantity
Perform stability studies and evaluate shelf-life data
Resolve chromatography and instrumentation technical issues
Document analytical methods for regulatory submissions
Provide technical guidance to junior analytical scientists
Requirements:
Advanced degree in Analytical Chemistry or Pharmaceutical Sciences
At least five years' pharmaceutical analytical development experience
Extensive HPLC and UPLC hands-on experience
Understanding of pharmaceutical quality and regulatory requirements
Solid analytical, communication, and problem-solving skills
Bring pharmaceutical development, stability testing, and validation expertise to analytical science work based in Kimberley.