Home / Job / Ipca Laboratories Limited – Walk-In Interviews for AMV / Quality Control on 20th Nov’ 2021

Ipca Laboratories Limited – Walk-In Interviews for AMV / Quality Control on 20th Nov’ 2021

Ipca Laboratories Limited – Walk-In Interviews for AMV / Quality Control on 20th Nov’ 2021

IPCA LABORATORIES LTD – Urgent Openings for Production, Maintenance,  Quality Control, Process Engineering - Daily Pharma Jobs

Walk-in Drive For Analytical Method Validation

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

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.Pharm

  • Experience: – 1 to 6 Years (Not for fresher)

Roles and Responsibilities:

– Quality Control

– GLP & QMS

– Instrumentation

– HPLC

– 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.

Regards

Shubham Joshi,

Ipca Laboratories Ltd.

Pithampur SEZ

[email protected]

T : 07292667008

E No : 108

Apply for this position

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