Company Name: Cadila Pharmaceuticals Ltd.
About Company: Cadila Pharmaceuticals
Limited is one of the largest privately held pharmaceutical companies in India,
headquartered at Ahmedabad, in the State of Gujarat. Over the last six decades,
the company has been developing and manufacturing pharmaceutical products in India
and selling and distributing these in over eighty-five other countries around
the world. Focused strongly on Innovation and Research, the company is present
in more than forty-five therapeutic areas spread across twelve specialities.Cadila
Pharmaceuticals has a multicultural, multilingual and multinational workforce
of more than seven thousand employees including over two hundred people outside
India in Africa, CIS, Japan and USA.
Job Type: Walk-in For API Unit
Departments: Quality Control
Designation: Officer To Executive
Job
Responsibility & Profile:
To
maintain and adherence of the GLP and safety procedures in laboratory.
To
raise the request for issuance of work data sheet / protocols.
To
maintain instruments log books properly as per analysis.
To
acquire training from concerned person to update the cGMP system update
technical knowledge.
To
perform the analysis as per work allocation and records the results in work
sheet / protocol and maintain on line documentation.
To
work as Analyst / Operator as a level of users and maintain the CFR 21 part -11
compliance by following laid down procedures.
To
perform all the HPLC related analysis of In-process, intermediate, finished
products & returned goods / raw materials Hold time / Stability study
/reference / working standard analysis as per laid down specification &
test procedures , SOPs, as per work allocation and report the analysis data in
LIMS modules and report to Section Head / Or QC head.
To
ensure that every specification and method of analysis used of right
product/material code.
To
follow the instruction of Shift /Section In charge for analysis /planning.
To
report any QI/NQI/OOS/OOT / Deviation/ discrepancy in laboratory analysis to
QC- In charge.
Responsible
for performing calibration of laboratory instruments as per schedule and laid
down SOPs with documentation and updation of instrument calibration status tag.
To
record and ensure all the entries, and results are in line with current
specifications and STPs.
To
prepare standard operating procedures, work data sheets and other documents
related to QC.
To
ensure the all column performance and column entry are maintain in column
logbooks.
To
record analytical data in work data sheets / protocols for raw material /
packing materials/intermediates /APIs and etc... As per current specification
and method of analysis.
Preparation,
qualification and management of working standard for Raw materials
Intermediates/APIs.
To
maintain reference / working standard/impurity standard usage records.
Review
of in-process analysis data and approval for further processing of the batch.
To
maintain instrument history record.
Joint
analysis with R&D personnel during analytical method transfer on HPLC.
Preparation
of stability protocols and stability reports.
To
perform analysis of stability samples as per stability schedule
Daily
monitoring and recording of temperature and humidity of refrigerator / working
standard chamber and laboratory area.
Perform
holding time study of intermediates and preparation of reports.
To
prepare/ check the protocols & reports for analytical method validation and
analytical method transfer
Inform
and Investigate OOS results in RM/Intermediates/APIs
Initiation
of change control / deviations / QI /NQI/ OOT related to QC.
Ensure
CFR 21 part -11 compliance and follow good chromatography practices during
analysis, integration and reviewing of on line and off line chromatographic
analysis to maintain proper data integrity.
Qualification Required: B.Sc. /M.Sc. , B.Pharma/ M. Pharma
Experience Required: 3 to 10 Years
Interview Date: 13th October 2017
Time of Interview: 11.30 To 3.30
Interview Location: Cadila Pharmaceuticals Ltd.
Plot No. 294, GIDC, Ankleshwar, Gujarat, India
Job Location: Ankleshwar
Contact Person & Details:
mayur.dalal@Cadilapharma.co.in 91-2646-252626
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