Walk-in for Quality Control and Quality Assurance on 06th January 2016 at Ankleshwar
Here is a chance to join Zydus at our API Manufacturing located at Ankleshwar as.
QUALITY CONTROL : Officers / Executive : M.Sc /B.Sc (Chemistry) with 2-8 years of hands on experience and relevant exposure in handling instruments like HPLC, GC, UV , wet lab and chemical analysis of Raw Material . Must be familiar with cGMP requirements. Shop floor Operation in API / Bulk Drug Manufacturing.
QUALITY ASSURANCE : Sr.Executive / Executive : M.Sc./ B.Sc Chemistry with 2-8 year , must be familiar with cGMP requirements, Data Integrity, Document Cell, Batch release process, Trending APR shop floor Operation in API / Bulk Drug
Manufacturing.
a) Data Integrity - Responsible to review of HPLC and GC , QC Sop Compliances, Investigation activities , OOS and OOT and quality control instruments.
b) Document Cell - Review of documents before DMF submissions, distribution / Issuance of BMRs, Master Formulae, SOPs and Formats to the respective departments and controlling all master documents.
c) Batch Release - Knowledge of ICH guidelines and should review of BMR;s and Validation documents and to give usage decision and dispatch of all APIs and salable intermediates in LIMS and SAP.
d) Technology transfer documents - Review and issuance TTD to plant , review of master batch record also review of specification and STP of API, Intermediate, RM, In-process.
e) Trending and APR - Knowledge of Market complaint, Deviation, Incident, Change control for trending of Systems, Review of Master SOPs, BMRs, PCRs, Trial batch reports, validation Protocols and reports and Annual Review reports.
Manufacturing.
a) Data Integrity - Responsible to review of HPLC and GC , QC Sop Compliances, Investigation activities , OOS and OOT and quality control instruments.
b) Document Cell - Review of documents before DMF submissions, distribution / Issuance of BMRs, Master Formulae, SOPs and Formats to the respective departments and controlling all master documents.
c) Batch Release - Knowledge of ICH guidelines and should review of BMR;s and Validation documents and to give usage decision and dispatch of all APIs and salable intermediates in LIMS and SAP.
d) Technology transfer documents - Review and issuance TTD to plant , review of master batch record also review of specification and STP of API, Intermediate, RM, In-process.
e) Trending and APR - Knowledge of Market complaint, Deviation, Incident, Change control for trending of Systems, Review of Master SOPs, BMRs, PCRs, Trial batch reports, validation Protocols and reports and Annual Review reports.
Date: 11th January 2016 (Monday)
Time: 09:30 AM to 05:00 PM
Venue: Cadila Healthcare Ltd.
Plot No.291,
GIDC Industrial Estate,
Ankleshwar-393 002.
Dist-Bharuch. Gujarat.
Contact No of HR representative: 02646-660408 / 660507
Candidates having experience of working in regulatory approved plants and possesses sound knowledge of documentation, cGMP and SAP will be preferred.
Those who are unable to attend the Personal Interview may send their resume through e-mail at ank.hr@zydusmail.com
Please mention the position applying for on the top of envelope or subject in case of e-mail.
Preference will be given to candidates having API - Pharmaceutical Industries experience.
No comments:
Post a Comment
Note: only a member of this blog may post a comment.