Walk-In Interview for QC / QA / AR&D /
FR&D- Trainee Scientist
Walk-in Interview for Fresher Candidates at
Stabicon on 02/02/2020, Sunday , Between 10am to 12pm.
Walk-in Interview Position & Scheduled
Details.
Position :
QC / QA / AR&D / FR&D- Trainee Scientist.
Qualification :
M.Sc/M.Pharm/B.Sc/B.Pharm.
Experience :
0 to 1 years in Pharma Industry.
Date & Time :
02/02/2020 Sunday, Between 10 am 12 pm
Venue :
Stabicon R&D -
Bommasandra.
Research &
Development Centre: Plot No. 28,
Bommasandra Industrial
Area (Sub-layout),
4th Phase, Jigani Hobli,
Anekal Taluk,
Bangalore - 560 099
Mob-7022281070
e-mail: hrd@stabicon.com
Role & Responsibility: QC / AR&D -
Trainee Scientist.
· Having
knowledge in current GLP requirement and analytical instruments like HPLC,
UPLC, GC and Dissolution tester etc.
· Daily
Calibration of instruments -balance, pH meter, Temperature and RH monitoring.
· Analysis
of wet lab activities-Water content, pH checking, weight/mL, DT, Hardness
testing etc.
· Calibration
of instruments.
· Analysis
of samples (routine, stability)
· Analytical
method development of Assay and dissolution by UV, HPLC and UPLC.
· Maintain
the laboratory and ability to produce high quality outputs.
Role &
Responsibility: QA - Trainee Scientist.
· Continuous
monitoring and reviewing of QMS and obtaining of updated regulatory information
and implementation in laboratory.
· Conducting
of internal audits, handling of customer complaints, investigation and Quality
checks.
· Issuance
of Analytical work records for calibration of equipments, routine, stability
and samples.
· Issuing
of work records for method development, method validation and method transfers
including change control, OOS and OOT.
· Preparation
of COAs for Routine samples and Method validation samples.
· Daily
monitoring of the temperature and relative humidity.
· Review
and approval of Routine sample and method development protocol in LIMS
· In
absence of duties, the responsibilities are handed over to Sr.
Person/Officer-QA
Role & Responsibility: FR&D
-Scientist.
· Literature
search, patent search, Reference product characterization, API and Excipients
Characterization etc. for initiating the project studies.
· Preparation
of Literature survey report & Development strategy report.
· Execution
of lab development trials, LNB writing and Submission of Sample for Testing.
· Execution
of optimization studies.
· Write
the Stability Protocol, sample preparation and submission of sample for
stability charging.
· Co-ordinate
with CSC Department for forwarding Samples to AD for analysis of Trial &
Stability samples, Co- ordinate with AD for analysis of trial & stability
products.
· Maintaining
on line documentation (Updating the log Books, at the time of instrument
usage.)
· The
equipments in the laboratory shall be utilized for minimum of 80%. The
breakdown of the equipments in the laboratory shall be reported.
· Updating
the log books, Status board, proper labeling of used accessories
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