Walk-In for
Quality Control Executive /Sr. Executives on Saturday
Dear Candidates,
We have arranged the Walk -In for Quality
Control for Executives and senior executives with 3 - 5 Years work experience
on 31 Aug’ 2019 between 9 am to 2 pm,
Interested candidates Kindly walk-In to the below venue .
Venue :-
Cipla Limited,
Plot No.285, 286,287,
Bommasandra Jigani Link Road
Industrial Area, KIADB 4th Phase,
Bangalore -560105.
Land Mark :-Towards HCL Technologies towards Jigani Industrial Area
Job description :-- Should Plan day to day Activities to the team guys & organizing training wherever required.
- Handling of Finished Products , Intermediates bulk finished, Raw material & -Packing material, stability samples, Purified water, potable water, raw water.
- Proper Documentation to comply all the requirements of CGMP.
- Should have knowledge on quality systems like SOPs, guidelines.
- Should have handled OOS, OOT and Lab error (Deviation).
- Review the Sampling of Finished Products & intermediates.
- Environmental Monitoring by Settle plate & Air sampler method.
- Handling of OOS, OOT and Lab error (Deviation).
- Handling of Calibration for analytical Instruments (i.e., HPLC, balance, pipette.
- System implementation as per regulatory requirement.
- Preparation of SOPs and implement the SOPs.
- Review and finalizing the report for Process validation, Method validation, and Cleaning Validation.
- Should have faced the Audit for MHRA, FDA, and Internal customer audits.
Knowledge in Current GLP/GMP
- IPQA activities
- Documentation
Land Mark :-Towards HCL Technologies towards Jigani Industrial Area
Job description :-- Should Plan day to day Activities to the team guys & organizing training wherever required.
- Handling of Finished Products , Intermediates bulk finished, Raw material & -Packing material, stability samples, Purified water, potable water, raw water.
- Proper Documentation to comply all the requirements of CGMP.
- Should have knowledge on quality systems like SOPs, guidelines.
- Should have handled OOS, OOT and Lab error (Deviation).
- Review the Sampling of Finished Products & intermediates.
- Environmental Monitoring by Settle plate & Air sampler method.
- Handling of OOS, OOT and Lab error (Deviation).
- Handling of Calibration for analytical Instruments (i.e., HPLC, balance, pipette.
- System implementation as per regulatory requirement.
- Preparation of SOPs and implement the SOPs.
- Review and finalizing the report for Process validation, Method validation, and Cleaning Validation.
- Should have faced the Audit for MHRA, FDA, and Internal customer audits.
Knowledge in Current GLP/GMP
- IPQA activities
- Documentation
Location of Work :- Bangalore
Thanks,
Thanks,
Great post, I have seen excellent expression in your writing. Being at the top for so many years is not as simple to do as it looks.
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