Stabicon Pharma Pvt Ltd. Walk -Interview For M. Sc/B.Sc,M.Pharm/B.Pharm Department QA/AR&D/FR&D/Microbiology On 11th August 2018
We are conducting walk-in interview on 11/08/2018 (Saturday), interview scheduled between 10am to 12pm.
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.
