Ajanta Pharma Ltd is hiring suitable fresher candidates for its US FDA formulation plant located at Paithan, Dist. Chh. Sambhajinagar, Maharashtra. The openings are in the QA department and are suitable for candidates with pharmacy or science qualifications and 3 to 5 years of relevant experience in formulation, qualification, validation, documentation and quality systems.
This is an email application opportunity for candidates who want to work in a regulated pharmaceutical formulation environment and contribute to quality assurance activities at a reputed pharma manufacturing site.
1. QA – B. Pharm / M. Pharm
Job Overview
| Department | QA |
| Qualification | B. Pharm / M. Pharm |
| Experience | 03 to 05 yrs. |
| Location | Ajanta Pharma Ltd, B-4/5/6 MIDC Area, Paithan, Dist.: Chhatrapati Sambhajinagar, 431148 |
| Application Mode | Email Application |
Responsibilities
- Work in an OSD formulation regulated plant environment.
- Handle QMS activities, Change Control, CAPA, Deviation and Market Complaints.
- Work with relevant QA software systems such as QMS, track-wise and E-log.
- Support documentation and compliance requirements related to quality assurance at the formulation plant.
Qualifications
- B. Pharm or M. Pharm qualification is required.
Key Skills and Experience Required
- 03 to 05 years of working experience in an OSD formulation regulated plant.
- Knowledge of QMS, Change Control, CAPA, Deviation and Market Complaint handling.
- Working experience with relevant software such as QMS, track-wise and E-log.
2. QA – B. Sc / M. Sc
Job Overview
| Department | QA |
| Qualification | B. Sc / M. Sc |
| Experience | 03 to 05 yrs. |
| Location | Ajanta Pharma Ltd, B-4/5/6 MIDC Area, Paithan, Dist.: Chhatrapati Sambhajinagar, 431148 |
| Application Mode | Email Application |
Responsibilities
- Prepare and review qualification and requalification protocols and reports.
- Execute qualification or validation studies.
- Review analytical reports.
- Support quality assurance activities connected with instruments, analytical test methods and validation documentation.
Qualifications
- B. Sc or M. Sc qualification is required.
Key Skills and Experience Required
- 03 to 05 years of relevant experience in QA activities.
- Experience in preparation and review of qualification / requalification protocols and reports.
- Experience in execution of qualification or validation studies.
- Ability to review analytical reports.
- Knowledge of various instruments and analytical test methods.
Why This Role Is a Good Opportunity
These QA roles offer an opportunity to work at Ajanta Pharma’s US FDA formulation plant in Paithan. Candidates with experience in regulated formulation manufacturing, QMS, validation, qualification and analytical documentation can apply for roles aligned with their education and experience.
How to Apply
Interested candidates can share their resume by email.
This communication is valid till Oct 30, 2026.


