1 Opening(s)
0 To 1.0 Year(s)
1.50 LPA TO 2.30 LPA
To perform all the activities of Quality assurance departments.
Ensure that SOPs are available for all quality related activities and they are current.
Prepare and review all quality assurance related documents such as SOPs, log book, format, etc.
Responsible for the Release of the final products.
Review batch sheet, packing sheet and final product ...
2 Opening(s)
5.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 10.00 LPA
Collecting and recording data day to day basis of different trials
Compile trial reports
Finding vendors for raw material/chemicals
Follow up for outside sample testing report/ pending purchase items / vendors for sample/quoteï‚· Working closely with the development team for planning part
Manage testing procedure and validation of new batches
Technical content
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
6.00 LPA TO 13.00 LPA
Responsible for Plant & Utility Instrument Maintenance activity.
Responsible for planning to review the SOP, Qualification, Validation, Temperature mapping and other activity.
Work permit from respective plants and execute the work as per priority of jobs and type of jobs.
Calibration documents review and planning of calibration of instruments.
Take trouble shooting action for ...
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
5.00 LPA TO 10.00 LPA
1. To perform all the activities of Quality assurance departments.
2. Ensure that SOPs are available for all quality related activities and they are current.
3. Prepare and review all quality assurance related documents such as SOPs, log book, format, etc.
4. Responsible for the Release of the final products.
5. Review batch sheet, ...
5 Opening(s)
4.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
1. To perform all the activities of Quality assurance departments.
2. Ensure that SOPs are available for all quality related activities and they are current.
3. Prepare and review all quality assurance related documents such as SOPs, log book, format, etc.
4. Responsible for the Release of the final products.
5. Review batch sheet, ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 10.00 LPA
To follow instructions given by Directors and Factory manager from time to time.
Follow formalized SOP and report to Factory Manager and QA in case of any changes or deviation or non-conformity.
To coordinate with QC at the time of Calibration.
To attend and fix major break down.
To coordinate with external agencies for ...
5 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 5.00 LPA
Job description
Role & responsibilities
Development of Analytical methods.
Validation of Analytical methods.
Preparing analytical method development reports.
Literature survey for existing analytical methods.
Carry out literature survey by establishing the strategies.
Maintenance of FDA department.
Coordinating various development activities in FDA laboratory.
Maintenance of reference standard, working standards and their standardization.
Co-ordinating the activities in Chemical and Instrumentation.
Analytical Method ...
1 Opening(s)
0 To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
To follow good documentation practices & good laboratory practices & encourage subordinate to maintain the same.
To ensure execution of safety precautions in the laboratory.
To perform daily operation & calibration of pH meter & balance.
To maintain hplc & gc column & hplc & gc instrument.
To record daily temperature monitoring of analytical ...
1 Opening(s)
3.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 5.00 LPA
1.0 Packing Activities.
1.1 Packing as per order given by marketing team.
1.2 Ensure Grade wise packing.
1.3 Take packing material for packing which is approved by QA and QC.
2.0 Supervision and Coordination of Shipment.
2.1 Confirm shipment.
2.2 Confirm requirement of packing type.
2.2.1 Ensure availability or minimum ...
5 Opening(s)
4.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
1. To perform all the activities of Quality assurance departments.
2. Ensure that SOPs are available for all quality related activities and they are current.
3. Prepare and review all quality assurance related documents such as SOPs, log book, format, etc.
4. Responsible for the Release of the final products.
5. Review batch sheet, ...