Walk-In Interviews @ Vivin Drugs & Pharmaceuticals Ltd
QC Chemist
(GC and stability study) Male candidates
Experience: 2-7 yrs
Openings: 10
Qualification: M.Sc
Job
description:
1.
Monitoring of stability Chambers, and
packing charging withdrawals of samples and incubation and analysis of
Stability Samples & Reporting.
2.
Analyzing Raw materials, Intermediates
and Finished Products using HPLC and GC.
3.
Efficient in handling various
instruments in wet lab like IR, UV,SOR.
4.
Calibration of Instruments like HPLC,
GC, IR UV SOR & Working standards Qualifications as per schedule timing.
5.
Handling of QMS
Documentation work like Preparation of STP and SOP
Warehouse
Executive
Experience: 1-5 yrs
Openings: 5
Qualification: Any Graduate
Job
description
1. Strictly adherence with cGMP norms.
2. Strictly adherence with Safety norms.
3. Responsible for following and ensuring safety guide lines are followed
by all personnel who are reporting.
4. Follow the Standard Operating Procedures and responsible for
cleanliness and good housekeeping.
5. Responsible for dispensing and distribution of raw materials and
packing materials.
6. Responsible for dispensing of all hazardous materials.
7. Responsible for receipts of all raw materials and packing materials.
8. Responsible for maintaining all stores related materials are stored
properly and in designated location.
9. Responsible for update the daily records Weighing Balance calibration
records,
10. Temperature records, Dispensing records, Cleaning records, Stock
Ledgers, Bin cards, Vacuum cleaning and usage records, and all check lists.
11. Responsible for receipts of all intermediate materials and
distribution to manufacturing blocks.
Research
Chemist (Male)
Experience: 1-5 yrs
Qualification: M.Sc
Job
description:
1. Follow and strictly adherent to GLP.
2. Performing the experiment in safe condition by using personnel
protective equipment as per approved procedures.
3. Responsible for preparing the Research Development Lab SOPs.
4. Outside samples and In-process samples receiving and informs to the
RDL manager and perform the experiment as suggested by Department
incharge/Designee.
5. Performing experiments with help of seniors.
6. Performing calibrations of all RDL related instruments as per
predefined schedules using approved procedures.
7. Approval of RDL reports which are prepared for In-process samples, raw
materials, water samples and intermediates for next stage in the absence of RDL
Head.
8. Keep the lab and all instruments always in clean and tidy condition.
9. Performing the batch process and observations of parameters with the
help of the assistants and reporting to RDL manager/Designee.
10. Making sure that the necessary calibrations are performed and records
kept.
11. Making sure that the premises and equipments are maintained and
records kept.
Date: 21st October, 9.30
AM - 4.00 PM
Venue:
Vivin Drugs & Pharmaceuticals Ltd,
Sy No:- 10 & 10D, IDA Kazipally, Gagilapur(vill),
Jinnaram(M.D), Sangareddy (D.t). Telangana
Contact - HR (8185069989)
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