Posted:16 hours ago|
Platform:
Work from Office
Full Time
* Exposure for Analysis and documentation of tablets, capsules, Liquid/Cream.
* Developing and validating analytical test methods for the testing of pharmaceutical products for manufactured to GMP and ICH requirements.
* Developing and validation of Cleaning Method validation.
* Transferring and documentation new analytical techniques to the Quality Control (QC) laboratory.
* Controlling laboratory chemicals required for analytical activities.
* Planning and organizing stability testing.
* Writing/reviewing specifications and methods of analysis.
* Writing/reviewing of Standard Operating Procedures (SOPs) as per regulatory requirement.
* Participating in self-inspections and regulatory inspections.
* Sample management and Documentation of RM and PM.
* Preparation and review of all analytical related documents.
* Working standard management.
* Handling of QC Instrument operation and Calibration related activity.
* Handling of OOS / OOT and Lab related incident / Investigation.
* Planning of daily activities of the laboratory.
* Must have skill of handling of HPLC Independently.
Orbit Pharmaceuticals
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