Saturday, February 1, 2020

Stabicon Walk-In Interview for QC / QA / AR&D / FR&D- Trainee Scientist on 02/02/2020 M.Sc/M.Pharm/B.Sc/B.Pharm.


Stabicon Walk-In Interview for QC / QA / AR&D / 

FR&D- Trainee Scientist on 02/02/2020 

M.Sc/M.Pharm/B.Sc/B.Pharm


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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