Are you passionate about advancing pharmaceutical excellence? Aizant Drug Research Solutions Pvt. Ltd., a leader in integrated drug development and manufacturing, is hiring for multiple Quality Assurance (QA) and Quality Control (QC) positions in Hyderabad, Telangana. Our walk-in interview on August 29, 2025, offers a chance to join a dynamic team dedicated to innovation and quality in pharmaceutical formulations. Explore exciting career opportunities in validations, IPFP, stability, raw materials, GLP, and material science lab roles. Don’t miss this opportunity to shape your future with a trusted name in the industry.
Job Responsibilities
As a QA or QC professional at Aizant, you will play a critical role in ensuring the highest standards of pharmaceutical quality. Responsibilities include:
- Validations: Conduct process and cleaning validations, and perform equipment qualifications to ensure compliance with regulatory standards.
- IPFP (In-Process and Finished Products): Execute analytical testing using HPLC, UV, dissolution, and related substances analysis.
- Stability: Manage stability sample testing, including dissolution, HPLC, and related substances, to ensure product integrity.
- Raw Materials: Perform sampling and testing of raw and packing materials to meet quality specifications.
- GLP (Good Laboratory Practices): Oversee standards management, column management, and analytical testing using HPLC, UV, and dissolution techniques.
- Material Science Lab: Conduct advanced testing using XRD, PSD, HPLC, DSC, TGA, ICPMS, and LC-MS/MS for nitrosamines and NDSRIs.
Qualifications
To excel in these roles, candidates should meet the following requirements:
- Validations: 4–5 years of experience in process/cleaning validations and equipment qualifications.
- IPFP: 2–4 years of experience with HPLC, UV, dissolution, and related substances testing.
- Stability: 4–6 years of experience in dissolution, HPLC, and stability sample management.
- Raw Materials: 2–3 years of experience in sampling raw and packing materials.
- GLP: 2–4 years of experience in standards management, HPLC, UV, dissolution, and column management.
- Material Science Lab: 3–5 years of experience with XRD, PSD, HPLC, DSC, TGA, ICPMS, or 2–5 years in nitrosamines and NDSRIs using LC-MS/MS.
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, or related fields.
- Strong knowledge of cGMP, GLP, and regulatory guidelines.
- Excellent analytical, problem-solving, and communication skills.
Benefits
Joining Aizant Drug Research Solutions offers:
- Competitive salary packages (₹4,00,000–₹8,00,000 annually, based on experience).
- Opportunities for career growth in a globally recognized pharmaceutical organization.
- Access to cutting-edge technology and training programs.
- Collaborative and innovative work environment.
- Comprehensive health and wellness benefits.
Application Instructions
Attend our walk-in interview to explore these exciting opportunities:
- Date: August 29, 2025
- Time: 9:00 AM onwards
- Venue: Aizant Drug Research Solutions Pvt. Ltd., Sy. No. 172 & 173, Apparel Park Rd, Dulapally Village, Dundigal – Gandimaisamma (M), Medchal – Malkajgiri (Dist.), Hyderabad, Telangana – 500100
- What to Bring: Updated resume, educational certificates, and ID proof.
Unable to attend? Email your resume to raghuveera.vutla@aizant.com. For more details, visit www.aizant.com.
FAQs
Q: What types of roles are available at the walk-in interview?
A: Aizant is hiring for QA and QC roles, including validations, IPFP, stability, raw materials, GLP, and material science lab positions.
Q: Can I apply if I miss the walk-in interview?
A: Yes, you can email your resume to raghuveera.vutla@aizant.com if you cannot attend the interview.
