Job  description

  • Prepare  CTD, ACTD  Dossiers and file regulatory submissions 
    • Perform assessments of new or revised products
    • Manage complaint documentation (including investigation and 
    • closure)
    • Respond to inquiries from regulatory bodies
    • Should be technically well versed with requirements for medicines with  fare  knowledge about medicines, food supplement,  
    • To Coordinate with relevant department for arranging documents
    • To prepare / compile dossier for allocated products / countries
    • To coordinate with account department for handling Local FDA fees / transfer of  amount for legalization etc
    • To coordinate with courier agency for dispatches of dossier /samples
  •  To make   timely entries of submissions / dispatches

 Qualifications : A bachelor’s degree in B. Pharma

Fresher and Experienced with (6 months to 3 yrs) both can apply.

Excellent communication skills

Should be aware about Microsoft office [word / Excel/ PPT] – Good in data  management

If your profile matches the above requirement and if you are interested in the above opening, kindly email your resume at the earliest as  attachment to [email protected] without changing the subject line.

If any of your friends / colleagues profile matches the above requirement, kindly suggest them to apply.

Contact Person: HR

Mobile No: 9311382870/8810226562

Mail ID: [email protected] 

Salary :- 13,000/- to 25,000/-

Position :- 2

Location :- Noida

Job Category: Drug Regulatory Affairs
Job Type: Full Time
Job Location: Noida

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