8.0 - 12.0 years

0 Lacs

maharashtra

On-site

The job involves preparing documentation for FDA, MDR, ISO, CE, GMP, or any other compliances as required by the company from time to time. You will be responsible for quality checking based on specific parameters and conducting factory visits for quality monitoring and execution. Additionally, you will be involved in incoming and outgoing QC validation, with a focus on ensuring compliance with quality standards. Proficiency in written and spoken English is essential for this role, along with good computer skills. Manpower management, handling stores/purchase, logistics, and new vendor development are also key responsibilities. Ideal candidates for this position should have a degree in B. Pharma or M.Sc. along with relevant experience in the field. The job type is full-time with a day shift schedule. Application Questions: 1. Do you have experience in preparing documents for FDA, MDR, ISO, CE, GMP 2. Do you hold a B.Pharm degree or M.Sc. with experience in a similar profile Preferred Experience: - QA/QC: 8 years Work Location: In person,

Posted 1 week ago

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