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3.0 - 7.0 years
0 Lacs
ahmedabad, gujarat
On-site
As the Quality Control Operations Manager in a WHO-GMP & ISO approved Tablets and Capsule manufacturing facility, your role involves the following responsibilities: - Performing HPLC and Dissolution analysis. - Reviewing and checking all Raw material, packing material, bulk and finish product specification, method of analysis, and all worksheets. - Reviewing and checking Different validation protocols like process, cleaning, analytical method. - Reviewing and checking Stability study and hold time study protocols. - Ensuring timely sampling and analysis of incoming materials, such as raw materials and packing materials. - Ensuring timely analysis of bulk, finish product, stability sample, an...
Posted 3 weeks ago
5.0 - 10.0 years
2 - 6 Lacs
sikkim
Work from Office
Job Description : Hands-on experience in -Perform the Analytical Method Validation by HPLC/GC Preparation and review of AMV Protocol and Reports operations and calibration of the instruments like HPLC, GC etc. Preferred candidate -Having 5 - 10 yrs of experience in Quality control and must have at least 2 years in AMV. Organisational Entity Zuventus Healthcare Ltd. Vertical ZHL Sikkim Factory Department Quality Control Continent Asia Country India Zone East Location Type S01-ZHL Factory
Posted 2 months ago
3.0 - 7.0 years
0 Lacs
ahmedabad, gujarat
On-site
This position is responsible for managing all Quality Control Operations of a WHO-GMP & ISO approved Tablets and Capsule manufacturing facility. Specific Responsibilities: To perform HPLC and Dissolution analysis. To review and check all Raw material, packing material, bulk and finish product specification, method of analysis and all worksheet. To review and check Different validation protocol like process, cleaning, analytical method. To review and check Stability study and hold time study protocol. To ensure for timely sampling and analysis of incoming materials, like raw materials, packing materials. To ensure for timely analysis of bulk, finish product, stability sample and validation sa...
Posted 3 months ago
2.0 - 4.0 years
2 - 3 Lacs
Boisar
Work from Office
Roles and Responsibilities Conduct quality control analysis using GC, HPLC, and other analytical methods to ensure compliance with regulatory requirements. Develop and maintain calibration protocols for laboratory instruments to ensure accuracy and precision of test results. Collaborate with cross-functional teams to resolve issues related to product quality and process optimization. Ensure adherence to cGMP guidelines and regulations in the pharmaceutical industry. Perform routine maintenance tasks on laboratory equipment to prevent downtime and ensure optimal performance. Desired Candidate Profile 2-4 years of experience in a similar role within the pharmaceutical or life sciences industry...
Posted 5 months ago
5.0 - 10.0 years
2 - 6 Lacs
Sikkim
Work from Office
Job Description : Hands-on experience in -Perform the Analytical Method Validation by HPLC/GC Preparation and review of AMV Protocol and Reports operations and calibration of the instruments like HPLC, GC etc. Preferred candidate -Having 5 - 10 yrs of experience in Quality control and must have at least 2 years in AMV. Organisational Entity Zuventus Healthcare Ltd. Vertical ZHL Sikkim Factory Department Quality Control Continent Asia Country India Zone East Location Type S01-ZHL Factory
Posted 6 months ago
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