Stabicon Life Sciences - Walk-In Interviews for QA / AR&D / FR&D / Microbiology on 11th August, 2018

We are conducting Walk-In Interview on 11/08/2018 (Saturday), Interview scheduled between 10 am to 12 pm.

Interested Candidates can attend walk-in interview at below address :
STABICON LIFE SCIENCES PVT. LTD.
Corporate Office:
M-413, H R B R 3rd Block, Near ICICI Bank
Kammanahalli Main Road,
Bangalore 560043, Karnataka, India.
Contact: hrd@stabicon.com or call +91 8095659882, 7022281070.
For More Information please visit : www.stabicon.com
For Experience Candidates Walk-in interview on 11/08/2018 (Saturday ) 
Department: QA / AR&D / FR&D/ Microbiology 

Positions:  Team Leader to Assistant Manager.
Qualification: M.Sc / M.Pharm / B.Sc / B.Pharm.
Experience: 5 to 9 years in respective area
JOB PROFILE FOR AR&D 

• Having adequate knowledge in current GLP requirement & all analytical instruments and like HPLC, UPLC, GC, Dissolution tester and UV-Visible spectrophotometer and etc.
• Having technical exposure on testing of RM , In-process and finished products of Various dosage forms as per GLP.
• Experience in Method development , Method validations and Method Transfer for analytical methods of dosage forms by using HPLC, GC and UV-Visible spectrophotometer as per current ICH guidelines and Pharmacopoeia.
• Having adequate knowledge in Preparation and review of analytical method validation/ method verification protocols, Method transfer/Routine/Stability documents 
• Having adequate knowledge for the review of analytical raw data & trend of stability samples.
• Ability to work in a multi-task environment & produce high quality outputs
• Having experience in planning / execution of projects as per timelines 

JOB PROFILE FOR QA. 

• Knowledge on Implementation, continuous monitoring and reviewing of Quality management system.
• Handling of QMS activities like CAPA , Deviation , Change control & Non-conformity
• Knowledge on conducting of internal audits, handling of customer complaints, investigations and Quality checks.
• Conducting training on latest regulatory requirements.(SOP training, On job-training & class room training)
• Responsible for work allocation & monitoring of regular activities, assuring of analytical results and releasing of COAs 
• Review& approval of Validation master plan and Qualification protocols for equipments , protocols , reports and work records
• Overall implementation and monitoring for effectiveness of stability procedure, activation of stability study in LIMS and approving of stability reconciliation.

JOB PROFILE FOR FR&D 

• Development of a formulation i.e from Literature survey to exhibit batches, preparing documents like literature reports, pre-product development strategy reports.
• Preparation, optimization and implementation of scale-up processes , execution of process evaluation and exhibit batches.
• Stability management Bench and lab scale along with preparation of Summary reports and preparation of stage wise Product Development Reports.
• Acquainted knowledge in USFDA, & ICH Guidelines.
• Preparing MFC (Master Formula Card),BMP (Batch Manufacturing protocol),BMR (Batch Manufacturing Record), Product Specifications (IP-FP), Protocols etc.
• Preparation of the SOPs, IQ, OQ & PQ for the equipment in R&D and maintenance of the logbooks.
• Acquainted knowledge in QbD concepts like indentifying critical process and
• Acquainted knowledge to prepare TTD and components for the development of the product.

JOB PROFILE FOR Microbiology 

• Responsible for smooth functioning of Microbiology department, work allocation and review of reports through ERP, Preparation ,Performance and Reviewing for all Microbilogical Methods Validation and Method Verification Documents.
• Knowledge on Microbial tests like MLT, Micro assays , Environment monitoring, PET is essential
• Knowledge on sterility testing 
• Preparation & review of SOPs for Microbiology related Equipments/Analysis, verifying and Reviewing of all Microbiological Samples Raw data reports, customer compliance of Microbiology .
• Knowledge on initiation of change controls deviations for Microbiology Equipments/Analysis
• Knowledge on investigation & handling of OOS for Microbiology Analysis
• Knowledge on Audit compliance report preparation
• Implementing new Microbiology technical requirements 
• Responsible for co-ordinating with vendors for IQ,OQ,PQ for new equipment/Instrument installation.
• Responsible for Media Growth promotion test, Sub Culture maintenance, maintaining of GLP, GDP in Microbiology Lab.