GLAND PHARMA LIMITED - Walk-In Interviews for Freshers & Experienced Candidates on 28th June, 2019


Walk-In Interviews for Freshers & Experienced Candidates
Greetings from Gland Pharma Ltd.We have an urgent requirement in our AR&D department in case if you are interested you can walk-in for an interaction on 28th June 2019 @ 09.00 AM to 11.30AM at the below address.
Venue: Gland Pharma Ltd.
Near Gandimaisamma cross roads,
D.P.Pally, Dundigal (post),
Hyderabad-43
Land Mark: Next to Dundigal Police Station
Contact Person. Mrs. Durgabhavani HR
Contact number : 040-30510999
Extension : 1025
Please carry the below for the interactionPassport size Photograph
Your updated resume
Copy of Education and Qualification certificates
Copy of Aadhar Card/ Pancard
Qualification for Freshers: B.Pharmacy / M.Pharmacy / M Sc(2018-2019) passed outs only.Experience: 0-2 Years
Venue: Gland Pharma Ltd.
Near Gandimaisamma cross roads,
D.P.Pally, Dundigal (post),
Hyderabad-43
Land Mark: Next to Dundigal Police Station
Contact Person. Mrs. Durgabhavani HR
Contact number : 040-30510999
Extension : 1025
Please carry the below for the interactionPassport size Photograph
Your updated resume
Copy of Education and Qualification certificates
Copy of Aadhar Card/ Pancard
Qualification for Freshers: B.Pharmacy / M.Pharmacy / M Sc(2018-2019) passed outs only.Experience: 0-2 Years
Job Description:
1. Responsible for literature survey & process development of New APIs.
2. Characterization of synthesized APIs and impurities.
3. Preparation of specifications for the raw materials used in the process, in-process checks and intermediate specifications in a process development.
4. Preparation of all process related documents for the new APIs developed.
5. LC-MS monitoring of impurities, process development (API) and finished products.
6. Preparative isolation and purification of impurities.
7. Conducting experiments regarding to impurity enhancements
2. Characterization of synthesized APIs and impurities.
3. Preparation of specifications for the raw materials used in the process, in-process checks and intermediate specifications in a process development.
4. Preparation of all process related documents for the new APIs developed.
5. LC-MS monitoring of impurities, process development (API) and finished products.
6. Preparative isolation and purification of impurities.
7. Conducting experiments regarding to impurity enhancements