Job Description:
* Instrumental analysis- Assay and RS by HPLC.
* Chemical analysis such as titrations, IR, SOR,U.V,ROI for routine analysis.
* Sampling,analysis and releasing of API's and Finished products.
* Adherence to safety and good laboratory practice (GLP).
* Participate in investigation of OOS and quality complaints.
* Maintaining of analytical documents as per cGLP.
* Performing the QC equipment Calibrations as per schedules.
* Handling and Inventory of stability samples.
* Handling of planned and unplanned deviations.
* Evaluation of reference standards and working Standards.
* Handling of Deviations and Incidents.
* Attending to SBPS, cGMP and OJT(on the job training) program to QC personnel.
* Motivating Good Manufacturing Practice & Safety Precautions.
* Checking of test results against standards,if any deviations and OOS observed timely report to section head.
* Maintaining Integrity of the SOP's,STP'S and Instrument log books
* Supporting for the process and cleaning validation work to production department.
* Handle any other assignment allocated by the section Head/Department Head.
APPLY HERE
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* Instrumental analysis- Assay and RS by HPLC.
* Chemical analysis such as titrations, IR, SOR,U.V,ROI for routine analysis.
* Sampling,analysis and releasing of API's and Finished products.
* Adherence to safety and good laboratory practice (GLP).
* Participate in investigation of OOS and quality complaints.
* Maintaining of analytical documents as per cGLP.
* Performing the QC equipment Calibrations as per schedules.
* Handling and Inventory of stability samples.
* Handling of planned and unplanned deviations.
* Evaluation of reference standards and working Standards.
* Handling of Deviations and Incidents.
* Attending to SBPS, cGMP and OJT(on the job training) program to QC personnel.
* Motivating Good Manufacturing Practice & Safety Precautions.
* Checking of test results against standards,if any deviations and OOS observed timely report to section head.
* Maintaining Integrity of the SOP's,STP'S and Instrument log books
* Supporting for the process and cleaning validation work to production department.
* Handle any other assignment allocated by the section Head/Department Head.
APPLY HERE
23 AUGUST 2014 –WORKSHOP ROUTE MAP DETAILS
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"Introductory Session for Career Opportunities in Clinical Research & Pharmacovigilance"
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DATE – 23 AUGUST 2014
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TIME – 10:00 am – 01:00 pm
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(*You need to appear @ 09:30 am, late candidates will not be allowed)
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(*Expert talk delivered by distinguished professionals from Industry)
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For any query- Call @ 092 898 70004 or mail to dheeraj.awasthi@cliniindia.org
Address – CLINI INDIA NOIDA, LEVEL 5, TOWER C, PLOT No. B9/A, Green Boulevard, Opp. Symbiosis University, B Block, Sector 62, NOIDA – 201301
*See route map for more details
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FREE INTRODUCTORY SESSION ON CLINICAL RESEARCH AND PHARMACOVIGILANCE
Still you don't applied for session ???
Fill the form now to utilize this Golden Opportunity "DELHI" - |
Clini India Noida (23 August 2014 -10:00 am - Only Registered candidates)
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Click on link for details, if you are Pharma/Medical/Biotech /Life Science fresher &; don't know how to get good Job in Industry -https://www.facebook.com/events/329935733832275/ |
Attend a workshop on 23/August/2014 Clini India Noida, without paying any amount - Get guidance by experts from Industry - Register for workshop by filling the form below |
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