Gland Pharma Limited – Walk-Ins on 25th July’ 2022 for Freshers & Experienced -

A holistic objective of dispensing health through a portfolio of injectable products across various therapeutic segments and delivery systems, has helped us expand to seven manufacturing facilities in India, with a capacity of approximately 750 million units. These include four facilities with 22 production lines for finished formulations and three Active Pharmaceutical Ingredient (API) facilities. Our products are produced at world-class manufacturing facilities and conform to global compliance, regulatory and quality specifications.

Vacancy Details

Walk-in – QA Validations @ Gland Pharma, Hyderabad

Designation : Trainee/officer/Executive.
Qualification : B Pharmacy/M Pharmacy/B Tech (Mech, E&C, EEE)/Diploma
Experience : 0 to 5 years
Location : Dundigal

Job Description :

Validation of Process Equipment’s such as autoclave, Tunnel, sterilizer, filling & Sealing machines.
Validation of HVAC Equipment’s.
Validation of BOD Incubator, Cooling cabinet & Stability chambers.

Documents Required :

1) Photocopy of Education Certificates.
2) Photocopy of Aadhar card & Pan card.
3) Latest three months pay slip from the present employer with supporting bank statement/ CTC Structure or latest increment letters.
4) Updated Profile.

Please walk-in on 25.07.2022 from 9.00 AM to 10.30 AM.
Venue Details : Gland Pharma Ltd.Near Gandimaisamma cross roads, D.P.Pally, Dundigal (post), Hyderabad-43
Land Mark: Next to Dundigal Police Station

Walk -In for QC – Chemist @ Gland Pharma, Visakhapatnam

Roles and Responsibilities:

1.Preparation of Standard Operating Procedures, General Test Procedures, Specifications and Standard Test Procedures.
2.Analysis of In process Samples, Finished, Raw Materials and Stability Samples.
3.Validation and Verification of Methods.
4.Calibration of Instruments.
5.Reviewing of Analytical Data.
6.Inform OOS, OOT and OOC to Supervisor.
7.Preparation and Review of COAs.
8.Preparation of Protocols and Reports.
9.Maintain Online Entries of Reference / Working Standards, Column Log Books, Instrument Log Books.
10.Maintain Related Raw Data and Log Books.
11.Maintain Good Laboratory Practices.
12.Maintain Good Documentation Practices.
13.Maintain Hygienic Conditions and Following Dress Code in QC laboratory.
14.Verification of Raw Data, Log Books and Reports.