Walk-In Interview at Aizant for QA & QC Professionals – Formulation Unit, Hyderabad
- Walk-In Interview at Aizant for QA & QC Professionals – Formulation Unit, Hyderabad
- Interview Details
- Job Openings at Aizant
- Eligibility Criteria
- How to Apply
- Summary Table
QA & QC Jobs at Aizant Drug Research Solutions | Walk-In Interview on 13th June 2025 | Hyderabad | B Pharm, M.Pharm, MSc Candidates
Aizant Drug Research Solutions Pvt. Ltd. is conducting a walk-in interview for experienced professionals in Quality Assurance (QA) and Quality Control (QC) at its formulation unit in Dulapally, Hyderabad. The recruitment drive is scheduled for 13th June 2025 (Friday) from 9:00 AM to 1:00 PM.
Apply now for QA & QC Pharma Jobs | Walk-In Interview | B Pharm, M.Pharm, MSc | Hyderabad | Formulation Unit
Walk-In Interview at Aizant for QA & QC Professionals – Formulation Unit, Hyderabad
Aizant Drug Research Solutions Pvt. Ltd., a leading pharmaceutical research and manufacturing organization, is inviting applications from skilled professionals for QA and QC roles in its formulations division. This is an excellent opportunity to grow with a company known for quality, innovation, and regulatory compliance.
Candidates with expertise in SOP review, HPLC, GC, Dissolution, Method Validation, and Environmental Monitoring are encouraged to attend the interview.
Interview Details
- Date: 13th June 2025 (Friday)
- Time: 9:00 AM to 01:00 PM
- Venue: Aizant Drug Research Solutions Pvt. Ltd., Sy. No. 172 & 173, Apparel Park Road, Dulapally Village, Dundigal Gandimaisamma Mandal, Medchal-Malkajgiri District, Hyderabad, Telangana – 500100
Job Openings at Aizant
Department: Quality Assurance (QA)
- Roles & Responsibilities:
- Review of SOPs and specifications
- Line clearance in Production, Warehouse, and Dispensing areas
- Experience Required:
- 6–8 years for SOP and specification review
- 2–4 years for line clearance activities
- Educational Qualification: B Pharm / M.Pharm / MSc (Life Sciences / Chemistry)
Department: Quality Control (QC)
Functional Areas & Experience:
- IPFP Stability:
- 4–5 years in HPLC, UV, GC, Dissolution, Related Substances
- Raw Materials:
- 4–6 years in Dissolution, HPLC, Sample Management, Related Substances
- Analytical Method Validation:
- 2–3 years in raw/packing material sampling
- 3–5 years in Method Validation, HPLC, Dissolution
- Microbiology:
- 2–3 years in Environmental Monitoring, Media Preparation, and MLT Testing
- Function Areas: AQA / IPQA
Eligibility Criteria
- Education: B Pharm / M.Pharm / MSc (Chemistry, Microbiology, Life Sciences)
- Experience: 2 to 8 years depending on the role
- Location: Dulapally, Hyderabad
- Documents to Carry: Updated resume, copies of educational certificates, ID proof
How to Apply
If you’re unable to attend the walk-in, send your resume to: raghuveera.vutla@aizant.com
For immediate consideration, walk in with your credentials on 13th June 2025. This could be your next big career move in pharmaceutical QA/QC!
Summary Table
| Company Name | Aizant Drug Research Solutions Pvt. Ltd. |
|---|---|
| Vacancy Departments | Quality Assurance, Quality Control |
| Required Education | B Pharm, M.Pharm, MSc |
| Experience Required | 2 to 8 years (role-specific) |
| Location | Dulapally, Hyderabad, Telangana |