Aurobindo Pharma Limited - Urgent Openings in Production / Engineering / Analytical QA - Apply Now
Urgent Openings in Production / Engineering / Analytical QA
Technical Assistant – Production (Pharma Formulations – OSD)
Location: Hyderabad
Job Description:
Operation of Compression, capsule filling, coating and Granulation
· Review of E-BMR
· cGMP compliance for the Production area
· Preparation, review, training of standard operating procedures
· Production activities-Planning daily, weekly and monthly.
· To ensure the conformance of systems and work practices with the SOP.
Required Candidate profile
Production with min 2-8yrs experience in Pharma Mfg - Formulations
Preferably in (Tablet, capsules) with
1. Qualification: ITI/Diploma/Any Graduate
2. Granulation,Capsule filling,Compression
Executive – Engineering (Documentation) Pharma Formulations
Job Description:
Engineering Document compliance (QMS)
Preparing of CCF, CAPA, QRM and investigation for deviations
Preparation and revision of engineering SOP
Review of engineering schedules -PM, calibration filter cleaning...
Required Candidate profile
Engineering (Maintenance) with min 2-6 yrs experience in Pharma formulations pref. in Sterile Injectables having experience in
Documentation
QMS (Engineering document compliance)
Preparation of CCF, CAPA, QRM
Analytical QA – Executive (Pharma Formulations OSD)
Experience: 3-8 yrs
Job Description:
Review of analytical reports Raw material, Packing material, In process, Stability study, analytical method validation protocols/ reports, Calibration, instrument qualification, Working standard qualification, analyst qualification etc. for compliance of the data as per statutory
Review of analytical reports Raw material, Packing material, In process, Stability study, analytical method validation protocols/ reports, Calibration, instrument qualification, Working standard qualification, analyst qualification etc. for compliance of the data as per statutory
Verifications of Certificate of analysis
Responsible for Review of QMS Documents (e.g. OOS, OOT, Incident, Deviation and Change control).
Responsible for review of electronic data to ensure the data Attributable, Legible, Contemporaneous, Original & Accurate.
Responsible to handle regulatory inspections
Review of SOP's related to Quality Control.
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