JOB DESCRIPTION:
Job Description
Version. no.:00
Name: : 738570
Division-Location: EPD-Baddi
Department: QC
Designation: Executive-QC
Grade/Band:
Reporting to: Manager-QC
Date of Joining:
Qualification : M.Sc. Chemistry
Experience (as on date) :
Followings will be the Core Job Responsibilities of the position holder:
Analysis and review of Inprocess, SFG, Finished Goods, Raw material & stability sample and related documentation as per GLP and GMP in time.
Ensure analysis and Review of RM, Stability and FG samples for Fenopenta, and other Export project sample.
Ensuring the timely updation in the documents as per the Pharmacopoeial amendments.
Timely charging and withdrawal of samples from stability chambers and their documentation within the time frame Sample reconciliation and destruction record of stability sample.
Data entry in Starlims.
Monitoring of stability chamber data.
Reporting of stability/Finished product sample as per report received from outside laboratory and check the compliance against respective specification.
Calibration of instruments, as and when required.
Preparation of volumetric solution, reagent and test solution, as and when required.
Implementation of GLP / GMP requirements.
Coordinating and aligning the practices and procedures in line with the COBC requirements
To play a training coordinator role in Isotrain system for training and compliance as per electronic system within timeline
In absence of the position holder, the sub-ordinate Executive / Manager working in the section or the authorized designee (as applicable) shall be responsible for day to day working.
The base pay for this position is
N/A
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:Operations Quality
DIVISION:EPD Established Pharma
LOCATION:India > Village Mauza : Baddi
ADDITIONAL LOCATIONS:
WORK SHIFT:Standard
TRAVEL:Not specified
MEDICAL SURVEILLANCE:Not Applicable
SIGNIFICANT WORK ACTIVITIES:Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)
