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2.0 - 5.0 years
4 - 7 Lacs
hyderabad, telangana, india
On-site
Should have sound knowledge of FDA documentation (Domestic and Exports). Should have multi-tasking attributes and should have excellent communication skills to interact with FDA authorities / Overseas Customers. Should be able to plan and execute the FDA activities as per requirements and should be flexible to manage the priorities. Should be well versed with requirements / guidelines of local and other state's FDA authorities. Should have enough knowledge and experience of coordinating with FDA for new applications / renewal of applications pertaining to Loan mfg. license, NOC s, Test Licenses, Product Permissions, COPP, FSC, NSQ, WHO-GMP and other technical documents. Should be responsible...
Posted 3 days ago
3.0 - 8.0 years
3 - 4 Lacs
gurugram
Work from Office
Position: Pharma Quality Control Officer - FDA Schedule M Documentation Qualification: Min. B. Pharma degree (mandatory) Location: Gurgaon, Haryana Experience: Min. 3 years Salary: Open/Negotiable - based on qualification, experience, and candidates expectation. Candidates are requested to mention their expected salary in the application / resume. Key Responsibilities: Ensure compliance with Schedule M requirements as per FDA and company SOPs. Prepare, review, and update QC/QA and other records, logbooks, and test reports. Maintain and review proper documentation in accordance with FDA Schedule M regulatory standards . Conduct sampling, testing, and analysis of raw materials, in-process mate...
Posted 3 months ago
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