Analytical Chemist

Responsibilities:

• Design and validate analytical methods for assessing raw materials, in-process samples, and finished products.
• Refine existing methods to boost accuracy, precision, and operational efficiency.
• Conduct routine and specialized testing of pharmaceutical products using techniques such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), UV-Vis Spectroscopy, and other analytical instruments.
• Perform stability studies to evaluate product shelf life under various conditions.
• Interpret analytical data to ensure it aligns with established specifications.
• Compile detailed reports, including analytical results, method development summaries, and validation protocols.
• Document all experimental procedures in line with Good Laboratory Practices (GLP) and company SOPs.
• Ensure all analytical processes adhere to Good Manufacturing Practices (GMP), FDA regulations, and other relevant guidelines.
• Assist in preparing regulatory documentation, including method validation reports and Certificates of Analysis.
• Collaborate with R&D and Quality Control teams to support product development, formulation, and production.
• Stay current with industry trends and advancements in analytical chemistry to continually improve processes and methodologies.

Qualifications:

• Bachelor’s degree in Chemistry, Biochemistry, or a related field. A Master’s degree or higher is a plus.
• Minimum of 2-4 years of hands-on experience in an analytical chemistry laboratory.
• Proficiency with analytical instrumentation and techniques, including HPLC, GC, MS, and FTIR.
• Strong problem-solving skills and the ability to interpret complex data.
• Familiarity with regulatory requirements and quality control standards.
• Excellent written and verbal communication skills, with attention to detail and accuracy.
• Ability to work independently and as part of a team in a fast-paced environment.