Regulatory Affairs - Senior Executive/Manager

Job Summary

Key Skills :

CTD, e-CTD format dossiers for non-regulated/semi regulated market, Artwork, cartons approvals

Experience:

5 - 10 Years

Specialization:

Registration, Quality Control, Q.A.

Job Function:

Regulatory Affairs

Industry:

Biotechnology/Pharmaceutical/Medicine

Qualification:

Post Graduation - M.Pharm, M.Sc School & Graduation - B.Pharm

Ultratech India Limited is an ISO certified Pharmaceuticals and Bulk drugs manufacturing firm based 
in Navi Mumbai.

Our manufacturing plant is located in Taloja MIDC and Corporate Office is at Vashi, New Mumbai.

Designation: Regulatory Affairs Executive/Officer.

Experience: Minimum 4 years in Quality Assurance Documentation for preparation of Drug Dossiers of a Formulations manufacturing unit.

Qualification : B.Pharm, B.Sc.

Candidate's Desired profile:
Past exposure in preparation of Drug Dossiers for regulated markets.

Previous Documentation exposure in various sections like tablets / capsules / Liquid orals / 
injectables preferred.

Knowledge of interpreting Q.C. reports.

Location: Vashi

Interested candidates please send your updated resume with the following details:
Current Salary, Expected Salary and Notice Period

e-mail ID: hrd@ultratechindia.com

Company Details [Ultratech India Limited]

Ultratech India Limited is an ISO certified Pharmaceuticals and Bulk drugs manufacturing firm based in Navi Mumbai. Our manufacturing plant is located in Taloja MIDC and office is at Vashi, New Mumbai.

Posted in: B.Pharmacy,B.Sc,Regulatory Affairs,vashi