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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