Research Associate Cadila Pharmaceuticals Limited

2.0 - 6.0 years

0 Lacs

gujarat

On-site

As a part of this role, you will be responsible for sample preparation, daily calibration, and the maintenance of equipment, including keeping a detailed log of all activities. You will also be involved in method development, method validation, and conducting sample analysis in accordance with ICH M10 guidelines. Operating, maintaining, and calibrating LCMS equipment will be a crucial part of your responsibilities. In addition, you will be required to adhere to documentation procedures as outlined in Bio analytical SOPs and ICH M10 guidelines. This will involve thorough record-keeping and ensuring all documentation is accurate and up to date. Furthermore, you will be expected to review data and reports to ensure quality and compliance with relevant standards. Your attention to detail, ability to follow guidelines meticulously, and commitment to maintaining accurate records will be essential for success in this role. If you are looking for a position that offers diverse responsibilities in a dynamic environment, this opportunity may be the perfect fit for you.,

Posted 2 days ago

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