Centaur Pharmaceuticals Pvt. Ltd.
WALK - IN INTERVIEW
Sunday, 17th April 2016 Between 9 am to 5 pm
VENUE :
Plot No-4, International Biotech Park, Hinjewadi Phase - II, Pune - 411 057. Ph: 020-66739400
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\Executive Quality Control/R&D:
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/R&D:
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\Executive Quality Assurance - Stability:
02 to 08 years of experience with regulated environment: Responsible for smooth operation of stability Section. Review of Stability Data ,stability protocol and reports. Handling of stability samples for regular, In-use, Freeze Thaw/Transportation/ Thermal cycling, Split tablet stability. Should understand the USFDA, Health Canada and EU requirement for stability in addition to ICH. Candidate should have expertise in analytical testing and requirements. Candidate should be well aware of data integrity concept, GLP practices. Should have knowledge of 21 CFR part 11, EU Annex 11 requirements.
Executive\ Sr. Executive Quality Assurance:
QMS :
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\Executive - R&D QA:
M.sc/M. 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
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