Executive - Pharma Regulatory Affairs
by PKG International in Delhi
Experience: 2 to 6 yrs. | Salary: INR 3,00,000 - 5,00,000 P.A | Opening(s): 3 Posted on: 05 Sep
Job Description
- Scrutiny of documents received from Pharma Companies and submissions of the same in DCGI office.
- Handling of Pharma Companies files pertaining to Biological Divn, Clinical Trials, Registration, NDAC, Vaccine Division, Registration, New Drug, Import, FDC, BE/NOC Test License,PSUR, Test License etc.
- Good contacts and personal rapport in all sections of DCGI Office
- Ensure receipt of various approvals in time bound manner.
- Adequate knowledge of Drug and Cosmetic Act.
- Good communication skill with internal & external organization.
- Good written & spoken english skills, good computer & documentation skills.
- Self-motivated, energetic personality
Salary: INR 3,00,000 - 5,00,000 P.A. Incentive and bonus
Industry: Pharma / Biotech / Clinical Research
Functional Area: Legal, Regulatory, Intellectual Property
Role Category: Drug Regulatory Affairs/Documentation
Role: Regulatory Affairs Manager
Keyskills: Experience as Technical Data Associate TDA in DCGI officeWork experience with a company dealing in Pharma Regulatory Affairs
Desired Candidate Profile
Education:
UG - B.Pharma - Pharmacy, B.Sc - Any Specialization
PG - Post Graduation Not Required
Doctorate - Doctorate Not Required
PG - Post Graduation Not Required
Doctorate - Doctorate Not Required
Should have experience in CDSCO as Technical Data Associate (TDA) and excellent contacts in all sections of this office. Candidates working with Pharma Regulatory Consulting Companies and having good knowledge of CDSCO working will also be considered..
Company Profile
http://www.newlifeindia.in
Contact Details
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