Reporting Analyst Jobs in Dholka
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Search Results - Reporting Analyst Jobs in Dholka
Cadila Pharmaceuticals Ltd-Dholka
related material / facility for projects. ? Responsible for RQA comments on SOPs, Protocols, Reports and study audits. ? Responsible for planning and execution of health monitoring of animal and employee. ? Collection of samples, analysis / dispatch...
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Cadila Pharmaceuticals Ltd-Dholka
and timely release of analytical reports. 5) As per requirement also perform the wet analysis.
Any Graduate
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Cadila Pharmaceuticals Ltd-Dholka
Principal task and Responsibilities: 1) Analytical Method Development by HPLC for all Project. 2) Routine HPLC Analysis for Raw Material, Intermediate, in process and Final API as per the Specification and Standard test procedure. 3) To maintain GLP...
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Cadila Pharmaceuticals Ltd-Dholka
1. Planning of analytical activity for assign Projects. 2) Review of Routine (F & D) and stability sample analysis as assign Projects and compilation. 3) Review of Specifications and Standard Test Procedures of Raw Materials, Finished Product...
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Cadila Pharmaceuticals Ltd-Dholka
JOB RESPONSIBILITIES
• Review of Literature summary report, patent summary report and development protocols.
• New product development, Planning and Resource allocation for Domestic, ROW, US, EU, CMO Market.
• Alternate source development for API...
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Cadila Pharmaceuticals Ltd-Dholka
documentation, training reports and records for Streptokinase and Botulinum -Maintaining records to comply with regulatory requirements. -Monitoring manufacturing processes and in process results of different unit operation Preparation and review of documents...
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Cadila Pharmaceuticals Ltd-Dholka
JOB RESPONSIBILITIES 1) Method development and report preparation. 2) Routine F&D and stability sample analysis. 3) Method development and report preparation 4) Analytical method verification of assigned products. 5) To perform the forced...
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Cadila Pharmaceuticals Ltd-Dholka
compound. 3) Preparation of protocol and reports of analytical method transfer activity. 4) Maintaining HPLC calibration report. 5) Maintaining analytical method validation raw data in workbook. 6) Trouble shooting during day-to-day analysis with proper...
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Cadila Pharmaceuticals Ltd-Dholka
Participate in the teleconference and clarify the client's technical issues 9) identify the needs of training and send the analyst for training. 10) Ensure the maintenance of all the analytical equipment's on regular basis 11) Review the developmental reports...
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Cadila Pharmaceuticals Ltd-Dholka
filled volume & weight method and leak test as per MMD-I & SOP. • To perform sampling of bulk and finished product for each batch at the end of the batch as per SOP entry into sampling log and submit the samples to QC for analysis. • Record review...
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Cadila Pharmaceuticals Ltd-Dholka
application and further analysis including statistical programs Preparation of raw data file, reports and specimen for archiving. Allied responsibility: 1. Following GPCB guidelines for waste management system and maintenance of its records 2.
To ensure pest...
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Cadila Pharmaceuticals Ltd-Dholka
JOB RESPONSIBILITIES 1) Preparation of analytical method validation protocol and report as per the current regulatory requirement. 2) As per protocol, perform the analytical method validation of titrimetric method, RS, Assay and Chiral etc.
for KSM...
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Cadila Pharmaceuticals Ltd-Dholka
for each location 10. Ensure timely vendor payments Principal Tasks and Responsibilities:
• 1.
Negotiation
• Ensure Quotations from different vendors are arranged as per SOP
• Verification of Comparative Analysis and negotiation
• Finalize the price...
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Cadila Pharmaceuticals Ltd-Dholka
compound. 3) Preparation of protocol and reports of analytical method transfer activity. 4) Maintaining HPLC calibration report. 5) Maintaining analytical method validation raw data in workbook. 6) Trouble shooting during day-to-day analysis with proper...
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Cadila Pharmaceuticals Ltd-Dholka
of Biotech.
• Destruction and disposal of documents after their shelflife.
• To maintain final scan copy of current MMD, MFC, Protocols, reports and SOPs.
• To prepare Editable ROAs.
• To revise Master Equipment list of Cadila biotech and CPLB facilities...
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