Zydus Cadila Walk in Interview for Quality Assurance, Quality Control & ADL - ONCO (R&D) on 24th December 2017, Sunday for Ahmedabad based API Manufacturing unit of Cadila Healthcare Limited. - My Hope Portal

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Monday, 18 December 2017

Zydus Cadila Walk in Interview for Quality Assurance, Quality Control & ADL - ONCO (R&D) on 24th December 2017, Sunday for Ahmedabad based API Manufacturing unit of Cadila Healthcare Limited.



Company Profile
Cadila Healthcare Limited
Zydus Cadila is a fully integrated, global healthcare provider, with strengths all along the pharmaceutical value chain. With a core competence in the field of healthcare, Zydus Cadila provides total healthcare solutions ranging from formulations, active pharmaceutical ingredients and animal healthcare products to wellness products. The group launched Exemptia, the world's first biosimilar for Adalimumab, the largest selling therapy worldwide for inflammatory arthritis. Zydus is also the only Indian pharma company to launch its own patented NCE - Lipaglyn, the world's first drug to be approved for the treatment of diabetic dyslipidemia. 
The group employs over 19,000 people worldwide and is dedicated to creating healthier communities globally. As a leading healthcare provider, it aims to become a global research based pharmaceutical company by 2020.

Designation: Officer / Executive / Senior Executive / Assistant Manager / Research Associate - Quality Assurance / Quality Control / ADL - ONCO (R&D). 


Date : 24th December 2017, Sunday
Time : 09:30 am - 01:30 pm
Venue : Cadila Healthcare Ltd. 
Sigma commerce Zone,
Nr. Iscon Mandir, BRTS Bus stand,
Ambli Bopal Road, Ahmedabad -380015.


Job Description  

Department : Quality Assurance
Designation :  Senior Executive / Assistant Manager
Experience : 04 - 07 Years
Edu. Qualification: B.Pharm / M.Pharm / M.Sc
Job Location : Ahmedabad 

Job Responsibilties: 
 Review and approval of all standard operating procedure (SOP).
Co-ordinate for activities in Analytical method transfer. 
Routine calibration/ verification of micro lab. Instrument/equipment as per schedule. 
Review of stability and Method validation data. 
To co-ordinate with R&D /ADL for technology transfer activities.
Review of all analytical data related to Standardization, intermediate, Finished APIs.
To investigate OOS/OOT/Incident/Deviations. 
Review of PRM, System Audit trail.
To monitor qualification, validation and revalidation activities at the site as per validation Master Plan. 

Department : Quality Control
Designation: Officer / Executive / Senior Executive
Experience : 03 - 05 Years
Edu. Qualification : Bsc / Msc
Job Location : Ahmedabad


Job Responsibilities: 

Preparation and review of SOP/STP/MOA/COA/Specification.
Preparation and review of Documents for Validation, AMV and Stability study.
Establishment of Good Documentation Practice and Good Laboratory Practice.
Handling trouble shooting for HPLC / GC & method development.
Operating & Calibration Sophisticated Instruments like HPLC, Gas Chromatography, UV-Spectrometer, Karl Fisher. etc.
Preparation of Documentation and Fill up Report.

Department : ADL - ONCO (R&D)
Designation: Research Associate / Senior Research Associate
Experience: 03 - 05 Years
Edu. Qualification :  M.Sc. (Chemistry) / M pharma (Analytical)
Job Location : Ahmedabad


Job Responsibilities :

Analytical method development of raw material, in-process samples, intermediate and Drug substances.
Analytical method validation of raw material, intermediate and drug substances as per ICH guideline.
Stability study as per ICH guideline.
Technology transfer of analytical method to plant QC.
Knowledge of instrument like pH meter, Karl fischer, Auto titrator ,HPLC and GC.
Day to day routine analysis activity i.e. instruments calibration, wet analysis, documentation and other.

Interested Candidates may walk in with updated CV & Salary proof.

FRESHERS NO NEED TO APPEAR IN INTERVIEW.

Preferance will be given to those candidates who are based at Ahmedabad or ready to relocate to Ahmedabad. 

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