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Monday, February 29, 2016

Officer\Sr.Officer\ Jr.Executive Quality Control at Centaur Pharmaceuticals FEB 2016

Centaur Pharmaceuticals Pvt. Ltd. Plot No-4, International Biotech Park, Hinjewadi Phase - II, Pune - 411 057. Ph: 020-66739400
Sunday, 28th February 2016 Between 9 am to 5 pm
Address : The Queeny Hotel, Airport Road, NH 17B, Velsao, Near Goa Airport, South Goa 403712 India, Phone : 0918322976577
Freshers and candidates with API experience are not allowed to attend.
Centaur, India's one of the fast growing Pharmaceutical Company having regulatory approvals of USFDA & MHRA is seeking deserving candidates for Pune Plant having experience in Formulation/Oral solid dosage and regulated market.
Officer\Sr.Officer\ Jr.Executive Quality Control:
02 to 06 years experience in handling of QC activities including operation of HPLC/GC system, non chromatographic analysis, review & documentation. Candidates must have exposure to work in regulated environment such as USFDA, MHRA etc.
Executive\Sr.Executive Quality Control:
05 to 08 years experience in regulated market QC laboratory with experience on handling & trouble shooting of chromatographic system such as GC/HPLC and non chromatographic system. Must have experience of handling of section such as RM, FP, GLP & stability. Candidate must have knowledge about current industry trends on GXP requirements, such as data integrity,21 CFR part 11,Annex 11 etc.
Officer\Sr.Officer\ Jr.Executive Quality Assurance:
02 to 06 years of experience with regulated market environment specifically for handling of vendor management, QMS Management and stability management. Candidate with QC experience having exposure in review of analytical data will be also preferred.
Executive\ Sr. Executive Quality Assurance:
5 to 8 years experience in regulated environment having experience in handling of QMS system such as deviation, CAPA, Vendor management, complaint, risk analysis etc.
Analytical QA : 05 to 08 years experience in QA department in handling of OOS, OOT, analytical data review, handling & trouble shooting of instrument such as GC/ HPLC, PSD & other QC activities. Candidate should be well aware of data integrity concept, GLP practices and must have knowledge of 21 CFR 11, Annex 11 requirements.
Officer/Sr. Officer Production:
02 to 06 years of experience of regulated market environment in Manufacturing operation of oral solid dosage form only.
(Machine Operator of granulation, compression, coating, blister and cartnator shall submit their resume or mail us on
Executive/Officer - R&D QA: Pharm with 02 to 08 yrs experience in well reputed formulation pharmaceutical company. Well versed with Documentation preparation and review and other R&D QA activities.
Required Qualification: Pharma Graduates / Post Graduates, Science Graduates / Post Graduates.
Interested candidates who are not being able to attend the interview can send their resume on for further process.


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