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Cdymax India Pharma in Jigani, Karnataka seeks a quality-focused candidate to oversee cGMP compliance, validations, stability studies, and analytical testing of raw materials and finished products.
You will manage laboratory teams, plan daily analyses, apply HPLC, GC, and UV-Vis methods, and assist internal and external audits while supporting continuous quality improvements with production.
Role & responsibilities
1.cGMP compliance, Validations, stability, Analysis of Pharma Raw Materials & Finished Products, Managing the laboratory teams and determining work priorities, Daily planning of analysis and ensure analysis of raw materials, intermediates, in-process controls, Proficient in various analytical techniques (e.g., HPLC, GC, UV-Vis spectroscopy) and knowledgeable about regulatory standards (e.g., ICH, FDA, EMA).
2.Familiarity with Good Manufacturing Practices (GMP) and Quality Assurance (QA) principles.
3.Strong analytical and problem-solving skills, with a keen attention to detail.
4.Assist in internal and external quality audits, ensuring compliance with relevant quality standards and regulations.
5.Work closely with production and other departments to resolve quality-related issues and support continuous improvement efforts.