Advance pharmaceutical method development through HPLC expertise as a Senior Analytical Development Scientist in hybrid Kimberley, Northern Cape, ZA. Develop reliable methods supporting product quality and integrity.
This senior scientist develops, validates, and implements methods for pharmaceutical products and intermediates. The work includes HPLC, UPLC, LC-MS, stability studies, and regulatory documentation. Collaboration with formulation scientists, process chemists, and quality control teams supports development activities.
Key Responsibilities:
Develop and validate HPLC analytical methods for pharmaceutical products
Optimize chromatographic conditions for separation and sensitivity
Troubleshoot analytical methods and instrumentation
Conduct stability studies and analyze degradation data
Prepare validation reports for regulatory submissions
Requirements:
Ph.D. or Master's degree in Analytical Chemistry or related field
Minimum five years' pharmaceutical method development experience
Hands-on HPLC and UPLC development experience
Proficiency in LC-MS is highly desirable
Knowledge of ICH guidelines, data software, and LIMS
Apply your HPLC, UPLC, and analytical development expertise to pharmaceutical quality work in hybrid Kimberley.
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