We are seeking a dynamic and detail-oriented Development Quality Assurance (DQA-Formulations) professional with 2-7 Years of experience to join our growing team. This role is critical to ensuring quality and compliance during the pharmaceutical product development lifecycle.
Location: Hyderabad(Dulapally)
Experience: 2-7 Years
🔍 Key Responsibilities:
📝 Preparation & review of departmental SOPs
📘 Review of BMR/BPR
✅ Perform line clearance activity
🔬 Conduct in-process checks during manufacturing & packaging
🧪 Sample & inspect process intermediates, residue, stability & finished products
📦 Collection & maintenance of reserve/reference samples
⚙️ Participate in instrument/equipment qualification execution
🧬 Monitoring & checks for pilot bio batches
🧾 Preparation & review of:
◾ Process validation / performance qualification protocols & reports
◾ Continuous process verification reports
◾ Cleaning validation protocols & reports
◾ Hold time study protocols & reports
📨 Send your resume to: raghuveera.vutla@aizant.com
⏳ Note: Immediate joiners are highly preferred!
ABAC

