Quality Control Analyst Jobs in Dholka
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Search Results - Quality Control Analyst Jobs in Dholka
Cadila Pharmaceuticals LtdDholkafreshersworld.com
schedule.
• To follow safety procedure in qc department.
• To receive the samples for analysis and making entry in Inward register.
• To maintain the Instruments log books related to sample analysis.
• To analyze the sample and compilation of documents...
Cadila Pharmaceuticals LtdDholkafreshersworld.com
Major purpose of the job : • Responsible for overall management of Biotech-QC department. Principal task and responsibilities : • Ensuring planning of the QC functional activities and sample analysis execution activity completed on time to reach...
Cadila Pharmaceuticals LtdDholkafreshersworld.com
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, To review the Batch...
Cadila Pharmaceuticals LtdDholkafreshersworld.com
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...
Cadila Pharmaceuticals LtdDholkafreshersworld.com
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, To review the Batch...
Cadila Pharmaceuticals LtdDholkafreshersworld.com
required)
• To receive the sample for analysis and making entry in inward register/LIMS.
• To maintain the report within QC Department.
• To provide the report to QA department for releasing the product.
• To enter the results in SAP/LIMS for maintain...
Cadila Pharmaceuticals LtdDholkafreshersworld.com
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...
Cadila Pharmaceuticals LtdDholkafreshersworld.com
validation/Hold Time/Packing Validation/Stability study as per respective protocols and to submit the samples to Quality Control for analysis. To notify the change control / Deviation related to shop floor activities. To review MMD-I / BPR and release...
Cadila Pharmaceuticals LtdDholkafreshersworld.com
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...
Cadila Pharmaceuticals LtdDholkafreshersworld.com
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...
Cadila Pharmaceuticals LtdDholkafreshersworld.com
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...
Cadila Pharmaceuticals LtdDholkafreshersworld.com
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...
Cadila Pharmaceuticals LtdDholkafreshersworld.com
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...
Cadila Pharmaceuticals LtdDholkafreshersworld.com
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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