Friday, June 25, 2021

Ind Swift Laboratories Openings for Drug Regulatory Affairs Sr Executive Executive

 Ind Swift Laboratories Ltd Walk-in interview 2021 for Drug Regulatory Affairs/ Sr Executive/Executive At Chandigarh.Ind Swift Laboratories Ltd Notification full detailes below.Interested Candidates Apply Now.

Important Vacancy details:

  1. Company Name:Ind Swift Laboratories Ltd
  2. Post Name: Drug Regulatory Affairs/ Sr Executive/Executive
  3. Qualification: Any Graduate in Any Specialization PG:Any Postgraduate in Any Specialization
  4. Experience: 01 to 6 year(s) of Experience
  5. Location: Chandigarh
  6. Salary:₹ 2,00,000 – 6,00,000 P.A.
  7. Openings:NA
  8. Contact Number:NA
  9. Selection ProcessThe selection will be on the basis of Interview.

Job Description: We have  Hiring For Drug Regulatory Affairs/ Sr Executive/Executive in Ind Swift Laboratories Ltd !

Required Candidate profile

  • Preparation of DMFs / amendments / Annual reports for various regions like US, Europe / Japan and ROW
  • Preparation of query responses
  • Preparation of LoA / LoE / CEP LoA / Cover letters / declarations
  • Review of Vendor documents
  • Review & archival of data
  • Co-ordination with plant / QA / R&D / QC for timely catering to documents / sample requirements for regulatory submissions.

How to Apply :

Step 1: Click on below link and you will be redirected to  Career Page of Recruiting Company or Career portal.

Step 2. Register on Career Page of the Company or  Career Portal by giving log in credentials and other personal or education details .

Step 3.Upon successful registration .User need to log in with credentials.

Step 4.Once logged in, User need to fill the all relevant personal ,educational  , Work experience details ,attach resume and submit application form.

Click here for notification and Apply

About Company: 

Ind Swift Laboratories Ltd.

We are looking for competent young professionals t o be an integral par t of our team

Ind-Swif t Laboratories Ltd is the fastest growing API Group. We are having 6 + API Manufacturing Facilities

across the globe. We are dealing in regulated market having approvals like USFDA, MHRA, TGA, ANVISA,

PMDA,EU GMP. We require energetic professionals with Regulatory knowledge of API / Bulk Drugs

Industry for our expansion plan.