About Company:
Ajanta Pharma Limited (APL) is a pharmaceutical company headquartered in Mumbai, India. It has strong presence in Branded Generic business in India & Emerging markets; and Generic business in USA. In India, company operates in selected therapeutic areas of Cardiology, Dermatology, Ophthalmology and Pain management. Its brands hold leadership positions in sub-therapeutic areas they are present in. In Emerging Markets, company has presence in Africa, South East Asia, West Asia, and CIS on broader therapeutic segments such as antimalarial, gastro, antibiotics, cardiology, dermatology, pain management, etc. As on 30th Sept 2024, Ajanta has 46 ANDA approvals which are commercialised. It holds 2 tentative approvals and 22 ANDAs are awaiting US FDA approval. Company plans to file 8-12 ANDAs during the current financial year. Company has state-of-the-art research facilities for formulation and API development located at Mumbai, India. R&D capabilities are evident from number of 1st to market products launched by the company providing patients most needed compliance and convenience. A dedicated and focused team of over 800 scientists work for R&D, which is growing continuously. Ajanta has 6 formulations manufacturing facilities located in India. Besides that, it also has an API manufacturing facility located at Waluj, India. Ajanta’s flagship formulation facilities at Paithan (Maharashtra, India) and Dahej (Gujarat, India) have been approved by US FDA. Ajanta continuously invests in enhancing the existing manufacturing facilities to meet current cGMP requirements and also construct new facilities to meet company’s growth requirements. Please visit https://ajantapharma.com/ for more information.
Vacancy Details:
Job description:
WE ARE HIRING
ap ajanta pharma limited
We are looking for suitable candidates for our US FDA approved formulation facility at Paithan, Dist. Chh. Sambhajinagar, Maharashtra.
Experience: 03 to 05 yrs.
Department: Officer – Quality Assurance
Education: B Pharma/M Pharma/M.Sc.
The candidate should have exposure of following-
1.Exposure to the OSD formulation FDA approved facility.
2.Should have QMS experience.
3.Investigation and review of deviations and incidents of QC.
4.Review and closure of change control of QC.
5.Closure of CAPAS of QC.
6.To check post effectiveness of change controls and CAPA of QC.
7.Trending of incidents, deviations and CAPA.
How to Apply?
Interested candidates can share resume cv.ptn@ajantapharma.com
This communication is valid till Jul 15, 2025
Location: Ajanta Pharma Limited, B-4/5/6, MIDC Area, Paithan, Dist: Chhatrapati Sambhajinagar, 431148
