Key Responsibilities:
• Responsible to analysis of in process, Finished
Product, Stability, raw material, Packing material and water samples.
• &nb
Key Responsibilities:
• Responsible to analysis of in process, Finished
Product, Stability, raw material, Packing material and water samples.
•
Responsible to prepare and review of Stability
protocol & analytical method validation protocol/Analytical method
verification/cleaning validation and their report.
•
Responsible to review of finished Product, in
process, Stability, raw material and water. Volumetric Solution Log book
entries
•
Responsible to analysis and review of standards
qualification for working standard & impurities.
•
Responsible to perform and review of all
instruments calibration and PM activity.
•
Responsible to conducting training program to QC
personnel.
•
Responsible to maintenance of Control
samples/Stability chamber with samples.
•
Responsible to preparation & review of Specification ,Standard testing procedure
(STP),ARDS and of Standard Operating Procedures (SOP’s) for Packing material, Raw material, IN-process
and Finished products.
•
Responsible for preparation and review of Log
Books / Sheets.
•
Responsible to prepare and review of
instrument/miscellaneous Qualification (IQ, OQ, & PQ) protocols and
reports.
•
Responsible to review of in process, Finished
Product, Stability, raw material, Packing material and water samples.
•
Responsible to initiate the change control,
deviation, &. Incident.
•
To ensure and control Good laboratory practices
in QC laboratory
•
Responsible for any other job responsibilities
as and when assigned by Senior or HOD from time to time.
Qualifications:
•
M.Sc./ M.Pharma/ B.Pharma/ BSc.
•
A minimum of 4-8 years.
•
Male candidates only.
•
Excellent problem-solving skills & good
communication and presentation skills.