Ipca Laboratories Ltd Walk-in Drive For Analytical Method Validation Department on 20th November 2021

 Walk-in Drive For Analytical Method Validation Department (AMV)

Date : – 20/11/2021 (Saturday)

Timing : – 10:30 AM to 05:00 PM

Venue : –  IPCA Laboratories LTD, 1, Pharma Zone, SEZ Indore Pithampur- 454775 (M.P.) 

Company : Ipca Laboratories Ltd (Formulation Unit)

Location : Pithampur SEZ (MP)

Department : AMV (Analytical Method Validation)

Qualification : B Pharm / MSc / M Pharm

Experience :  3 to 7 (Not for Fresher)



Job Responsibilities:


Should have good  knowledge about sophisticated instrument like Waters HPLC, Perkin GC system with Empower 3 software. 


Should have knowledge about Analytical method validation, Analytical method verification and Analytical method transfer as per various guidelines (like  ICH, USP etc) and cGLP requirement.


Aware about compliance of Laboratory with ALCOA, system SOPs, specification and method of analysis.


To prepare protocols and worksheet for analytical method validation, analytical method transfer and analytical method verification activities. 


To perform calibration of AMV instruments and equipment as per procedure in AMV Lab and have to review their documents.

To perform cleaning validation and have to  handle activities of QMS e.g. Incidents, Deviations etc.

Related documentation like SOPs, STPs, GTPs etc 


Regards

Shubham Joshi,

Ipca Laboratories Ltd.

Pithampur SEZ

shubham.joshi@ipca.com

 T : 07292667008

 

Walk-in Drive For Quality Control Department in GLP, HPLC and QMS

Date : – 20/11/2021 (Saturday)

Timing : – 10:30 AM to 05:00 PM

Venue : –  IPCA Laboratories LTD, 1, Pharma Zone, SEZ Indore Pithampur- 454775 (M.P.) 

Qualification: – B.Sc & B.Pharma

Experiance: – 1 to 6 Years (Not for fresher)


Roles and Responsibilities 


Should have good  knowledge about sophisticated instrument like Waters HPLC, Perkin GC system with Empower 3 software. 


GLP & QMS


To perform lab activity review like analytical data, change control, laboratory events, lab incident, OOS & OOC in quality control lab.


To carry out the full-scale comprehensive investigation of Out of Specification (OOS) and Out of Trend (OOT) observed in Finished Drug Product&Stability samples.


Should have knowledge about Analytical method validation, Analytical method verification and Analytical method transfer as per various guidelines (like  ICH, USP etc) and cGLP requirement.


To perform cleaning validation and have to  handle activities of QMS e.g. Incidents, Deviations etc.


To perform calibration of AMV instruments and equipment as per procedure in AMV Lab and have to review their documents.


Related documentation like SOPs, STPs, GTPs etc 


Regards

Shubham Joshi,

Ipca Laboratories Ltd.

Pithampur SEZ

shubham.joshi@ipca.com

T : 07292667008

Mob : 9911590055 (Fresher are requested not to call)

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