Our client who is a specialized CDMO within the pharmaceutical industry is looking for a seasoned Chemist to lead method development for various analytical methods. 

Key Responsibilities:

• Develop, optimize, and validate HPLC methods for the analysis of raw materials, intermediates, and finished pharmaceutical products.
• Troubleshoot and refine methods to ensure robustness and reproducibility.
• Prepare technical reports and documentation in compliance with regulatory requirements.
• Support QC studies and process development through method application.
• Collaborate with other departments, including R&D and quality control, to ensure accurate and timely analysis.

Qualifications:

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, or related field 
• Proven experience with HPLC and related analytical techniques in a pharmaceutical or laboratory setting.
• Experience in HPLC method development
• Strong knowledge of regulatory guidelines such as GMP 
• Excellent problem-solving and communication skills.