Posted:1 day ago|
Platform:
Work from Office
Full Time
Key Responsibilities: Develop and validate robust analytical methods (e.g., HPLC, GC, LC-MS, UV, FTIR) for drug substances, drug products, raw materials, and intermediates. Conduct routine and non-routine testing to support formulation development, stability studies, and process optimization. Maintain and troubleshoot analytical instrumentation and software. Prepare and review analytical documents such as protocols, reports, SOPs, and method transfer documentation. Ensure compliance with GMP/GLP, company SOPs, and regulatory requirements. Collaborate with formulation scientists, QA/QC, regulatory, and production teams to ensure seamless project progression. Analyze, interpret, and present data in internal meetings and for regulatory submissions. Participate in audits and regulatory inspections as needed. Best Regards Team Jodas
Jodas Expoim
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