Regulatory Affairs Jobs with Leading Pharmaceutical Company

By: Pharma Jobs | Views: 4690 | Date: 31-May-2015

It is a leading Active Pharmaceuticals Ingredients (API) Manufacturing Company in India. Company were started in 2006 and is headquartered at Surat, Gujarat, India. Company manufacture Active Pharmaceutical Ingredients (APIs), & Intermediates. Company has created a strong product portfolio, building on its R & D Expertise, regulatory capabilities and multi scale production capacities. Company has been established with a vision to become a major global player and as part of our vision we are already into reg

Regulatory Affairs Jobs with Leading Pharmaceutical Company


Dear Candidate,

Greetings from Vali Recruiters.... (A Job Placement Consultancy)

This is regards to your C.V. posted on the job portal and currently we have an urgent opening for the position of Senior Officer/ Junior Executive- Regulatory Affairs with the leading API Manufacturing Company based at Sachin Surat, Gujarat.


Company Details:


It is a leading Active Pharmaceuticals Ingredients (API) Manufacturing Company in India. Company were started in 2006 and is headquartered at Surat, Gujarat, India. Company manufacture Active Pharmaceutical Ingredients (APIs), & Intermediates. Company has created a strong product portfolio, building on its R & D Expertise, regulatory capabilities and multi scale production capacities. Company has been established with a vision to become a major global player and as part of our vision we are already into regulated market & our facility is approved by USFDA, EUGMP, KFDA, COFEPRIS, MOH, and PMDA.

Below mentioned are the job details:

Designation: Senior Officer/ Junior Executive- Regulatory Affairs

Qualifications: B.Sc/M.Sc/B.Pharm/M.Pharm

Job Location: Sachin, Surat, Gujarat

Salary will be competent with the industry.

Job Description:-
*To prepare and file dossier for USDMF/ CEP/EDMF/ DMF-Health Canada and any other countries as the requirement may be.
*Practical Knowledge of e-submission.
*To file amendments, revision/ notification to regulatory agencies and customer.
*Preparation of Technical Packages and open part
*Preparation of Drug Master Files and Dossiers
*Co-ordination with various functionaries to get the documents and review of the documents.
Candidate must have Experience of API (Active Pharma Ingredients) / Bulk Drug Manufacturing Plant.

Note:

Apply only those candidates who are really interested for job change and outstation candidate must be open for the relocation.
Interested candidates can send their latest resume on reply of this mail with the below mentioned details;

Current CTC:
Expected CTC:
Notice Period:
Total Experience:
Current Location:

DO NOT CHANGE THE SUBJECT LINE SIMPLY REPLY ME ON THE SAME MAIL WITH UPDATED RESUME.
Forward this mail to your friends who have the same experience and may be interested for this opening.

In case your profile does not match the above criteria then do not write / send any comments to us kindly ignore it. Kindly note that this is a part of mass mailing; your CV has been electronically selected, based on certain standard parameters. If any of your friends or colleagues may be interested, it would be more than my pleasure to help them out too.

Thanks & Regards

Manjari Basak
Executive - Recruitment
Vali Recruiters (A Placement Consultancy)
Ahmedabad
E-mail: vali.manjari@gmail.com
Website: http://www.valirecruiters.com



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Comments
p.janardhan  |  03-Jun-2015 07:23:40 IST
Gdmrng sir, i need job in regulatory affairs, if u r able to provide me job in RA, send me details
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