Quality Control Jobs in Dholka
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Search Results - Quality Control Jobs in Dholka
Cadila Pharmaceuticals Ltd-Dholka
Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of raw material on non-chromatographic instrument such as FTIR, UV, Polarimeter, KF, Autotitrator etc. by following test procedure. • To attend the training as per...
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Cadila Pharmaceuticals Ltd-Dholka
for Export and Domestic market. 6. To coordinate with Formulation and development, Quality Control and Regulatory Agency 7. Taking the Backup record of Raw material, Finished Product Specification and Standard Test Procedures. 8. Responsible for issuance...
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Cadila Pharmaceuticals Ltd-Dholka
Follow cGMP and GLP practices in Quality Control Lab.
• To monitor the stability program as per regulatory guideline and stability protocol.
• To allocate the stability sample to analysis and destroy after completion of analysis.
• To follow...
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Cadila Pharmaceuticals Ltd-Dholka
Follow cGMP and GLP practices in quality control lab.
• To prepare Specification Master as per STP in SAP/LIMS.
• To follow safety Procedure in QC department.
• Preparation of COA as per current specification for Packing samples (whenever...
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Cadila Pharmaceuticals Ltd-Dholka
Follow cGMP and GLP practices in Microbiology lab
• Penicillin QC
• To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP.
• To follow safety Procedure in Microbiology...
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Cadila Pharmaceuticals Ltd-Dholka
Follow cGMP and GLP practices in Microbiology lab
• Main pharma QC laboratory.
• To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP.
• To follow safety Procedure...
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Cadila Pharmaceuticals Ltd-Dholka
Follow cGMP and GLP practices in Microbiology lab
• Penicillin QC
• To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP.
• To follow safety Procedure in Microbiology...
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Cadila Pharmaceuticals Ltd-Dholka
with the quality control and production departments for technical specifications and material approvals. • Monitor vendor performance and ensure compliance with agreed terms and industry regulations. • Ensure all purchasing activities comply with cGMP, GDP, FDA, and other...
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Cadila Pharmaceuticals Ltd-Dholka
chambers daily temperature and humidity monitoring.
• To follow safety Procedure in QC department.
• Responsible for withdraw the stability sample for analysis as per schedule.
• To maintain stability study log book of stability sample.
• Responsible...
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Cadila Pharmaceuticals Ltd-Dholka
support to Formulation & Development, Quality Assurance, Quality Control and Regulatory Affairs teams. 9) Participate in analytical budgeting and resource planning for new and ongoing projects. 10) Planning for New scientist for analyst qualification...
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Cadila Pharmaceuticals Ltd-Dholka
10. Preparation of working standard as per SOP. 11) Analytical method transfer to QC Lab. 12) Cleaning and maintenance of laboratory equipment.
Any Graduate
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Cadila Pharmaceuticals Ltd-Dholka
ordinate with tablet sub
• department, Quality Assurance, Quality Control and engineering department to achieve production delivery as per production schedule.
• To ensure daily production report and submit to higher management.
• To ensure periodic...
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Cadila Pharmaceuticals Ltd-Dholka
for Ethiopia.
• Dispatch of material to Loan license and Ethiopia plant.
• Handling of retest, rejected, expired materials.
• Co-ordinate with quality control / production / maintenance /QA / SCM/ Purchase / Contract Mfg etc.depts.
For smooth functioning...
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Cadila Pharmaceuticals Ltd-Dholka
functional teams like QC, QA, Maintenance, Warehouse, Injection etc. 7. Training and mentoring new joinees 8. Keep the track for calibration and qualification activities, for example for equipment, weighing scale and standards etc.
Any Graduate
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Cadila Pharmaceuticals Ltd-Dholka
To coordinate with CFT team like AR Lab, Production, Manufacturing, QA/QC for timely completion of project. • Ensure timely address of regulatory deficiencies for Domestic, ROW, US, EU, and CMO Products. • Compilation and review of the FnD data, interpretation...
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