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2.0 - 6.0 years
0 Lacs
karnataka
On-site
Role Overview: You will be responsible for planning and executing various analytical method development and validation for new products, comprehensive testing of API and finished dosages while ensuring compliance with regulatory and safety requirements. You will review laboratory data, instrument logbooks, and reports when necessary. Additionally, you will initiate departmental change control requests and oversee the progress through the QMS system. Your role will involve preparing Transfer of Analytical Procedures (TAP) protocols and reports for various sites, along with procurement of samples and impurities as required. Key Responsibilities: - Prepare working plans for assigned projects an...
Posted 4 weeks ago
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