Vivin Drugs & Pharmaceuticals Ltd – Walk-In Interviews for Freshers & Experienced in Production / Quality Control on 3rd & 4th Nov’ 2020
WALK-INS @ VIVIN DRUGS & PHARMACEUTICALS LIMITED
Experience: 2 – 6 years
Strictly adherence of with cGMP norms.
Strictly adherence of with EHS, EMS & OHSAS norms.
Collecting records like BPRs and related documents from QA department.
Conducting the process operations and recording the process parameters progressively in BPR’s.
Responsible for maintaining discipline in the shift and also for keeping the production area in an orderly manner.
Co-ordinates with maintenance people in the shift for the smooth completion of routine and preventive maintenance jobs.
Attending the training programs periodically to improve knowledge and working skills to the desired levels.
Recording the data in online records like BPR`s, equipment use log and other related records.
Date & Time: 3rd November – 4th November, 9.30 AM – 5.00 PM
Quality Control Trainee
Experience: 0 – 5 years
Qualification: M.Sc / M.Pharm
Good Knowledge on elements
Good Knowledge on Structure
Experience: 2 – 6 years
Qualification: B.Sc / M.Sc / M.Pharm
QC Roles and Responsibilities:
Required candidates below experience candidate.
Monitoring of stability Chambers, and packing charging withdrawals of samples and incubation and analysis of Stability Samples & Reporting.
Analyzing Raw materials, Intermediates and Finished Products using HPLC and GC.
Efficient in handling various instruments in wet lab like IR, UV,SOR.
Calibration of Instruments like HPLC, GC, IR UV SOR & Working standards Qualifications as per schedule timing.
Handling of QMS
Documentation work like Preparation of STP and SOP
Date: 3rd November& 4th November, 9.30 AM – 4.30 PM
Vivin Drugs & Pharmaceuticals Ltd,
Sy No:- 10 & 10D, IDA kazipally, Gagilapur (Vill), Jinnararam (M.D),
Contact – Madhu (7729095441)
Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field.
During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube