Optimus Drugs - Walk-In Interviews on 15th December 2018 for R&D @ Hyderabad

Greetings from Optimus Drugs Pvt. Ltd!...

Walk -In Interviews for R&D Dept. on 15th Dec, 2018(Saturday)

Qualification: M Sc.

Experience: 1-3 Yrs

Department: API R&D

Contact Person: Mr. Abdul Gaffar

Mobile No : 9133332440

Date: 15th Dec, 2018(Saturday).

Time: 10.00 am to 04.00 pm

Venue:

M/s Optimus Drugs P Ltd,

Plot No: 73/B & 73/B/2, EPIP,

IDA Pashamylaram, Patancheru

Hyderabad – 502 307

You are advised to carry the below set of mandatory documents. 

1. Updated CV.

2. All Educational and Experience Certificates Xeroxes.

3. Aadhar Card and

4. Latest passport size photo.

5. Appointment Letter of Current Organization

6. 6 Months Bank Statement

7. 3 Months pay slip

Google Maps Link given for your better way to come:

https://goo.gl/maps/shRcymT18yC2

Please refer your friends.

Regards,

Team HR

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MSN Laboratories - Walk-In Drive on 15th December 2018 for Executive / Sr. Executive - Regulatory Affairs

Walk- In Drive for Regulatory Affairs in API Division- R&D Center
Regulatory Affairs API RA Dept. in API Division 
Job Description: (API Regulatory Affairs - API Division)
1. Should have minimum of 2 to 5 years of experience in API Regulatory Affairs
2. Thorough knowledge in US, EU and CA regions DMF submission procedures along with emerging markets such as Brazil, Taiwan, Japan, Russia, China etc
3. Should possess good response drafting skills to ensure that the responses to the regulatory queries are properly addressed
4. Should have knowledge and experience in eCTD submissions to US, CA and EU and troubleshooting the issues
5. Thorough review of regulatory submissions prepared by team members and to ensure the correctness of the documents or submissions.
6. Responsible for ensuring and sending response to all the technical queries received from various customers are properly responded as soon as possible.
7. Conducting meetings for the deficiency letters received from various regulatory authorities and tracking of deficiencies with respect to the target timelines and ensure that the response is sent to the authorities as per the stipulated timelines.
8. Participation in the Cross Functional Team (CFT) meetings and guidance to the product development team on regulatory issues.
9. Participation in the Technology Transfer Meetings and ensure that the product is meeting the regulatory requirements.
10. Responsible for ensuring that the regulatory database is properly maintained and updated.
11. Responsible for Review and approval of change control and should ensure that all the approved changes are reported to regulatory authorities.
Drug Regulatory Affairs API RA Dept.
Experience: 2 to 5 Years 
Position: Executive / Sr. Executive
Male Candidates Preferable .
Date of Interview: 15.12.2018 (Saturday)
Interview Time: 9.00 AM to 1.00 PM
Venue Details :
MSN Laboratories Pvt.Ltd.,
R&D Center, Pashamylaram
Ph No : +91-8452304799/4899
040-30438786
Work Location : Pashamylaram

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