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Required Sr. Executive Quality Assurance (IPQA) - B.Sc./M.Sc.(Biotechnology, Microbiology, Biochemistry, Life Sciences) /B.Tech Biotechnology or related disciplines

Required Sr. Executive Quality Assurance (IPQA). Hetero Plasma Sciences Ltd. is looking for experienced and passionate professionals to join their Quality Assurance (IPQA) team. Details are provided below  1. Position: Sr. Executive Quality Assurance (IPQA) 2. Location: Kothur, Telangana 3. Department: Quality Assurance (IPQA) 4. Experience: 4-9 Years 5. Qualification: B.Sc./M.Sc. (Biotechnology, Microbiology, Biochemistry, Life Sciences) /B.Tech Biotechnology or related disciplines 6. Key Responsibilities:  -Perform In-Process Quality Assurance (IPQA) activities during downstream processing operations. -Conduct line clearance activities and ensure compliance with GMP requirements. -Review plasma reconciliation activities and batch-related documentation. -Prepare and review MFRs, BMRs, SOPs, and other quality documents. -Possess knowledge of Chromatography and TFF (Tangential Flow Filtration) techniques and processes. -Participate in Process Validation, Cleaning Validation, an...
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Required Sr. Executive Quality Assurance (IPQA) - B.Sc./M.Sc.(Biotechnology, Microbiology, Biochemistry, Life Sciences) /B.Tech Biotechnology or related disciplines

Required Sr. Executive Quality Assurance (IPQA).
Hetero Plasma Sciences Ltd. is looking for experienced and passionate professionals to join their Quality Assurance (IPQA) team.
Details are provided below 
1. Position: Sr. Executive Quality Assurance (IPQA)
2. Location: Kothur, Telangana
3. Department: Quality Assurance (IPQA)
4. Experience: 4-9 Years
5. Qualification: B.Sc./M.Sc.
(Biotechnology, Microbiology, Biochemistry, Life Sciences) /B.Tech Biotechnology or related disciplines
6. Key Responsibilities: 
-Perform In-Process Quality Assurance (IPQA) activities during downstream processing operations.
-Conduct line clearance activities and ensure compliance with GMP requirements.
-Review plasma reconciliation activities and batch-related documentation.
-Prepare and review MFRs, BMRs, SOPs, and other quality documents.
-Possess knowledge of Chromatography and TFF (Tangential Flow Filtration) techniques and processes.
-Participate in Process Validation, Cleaning Validation, and Annual Product Quality Review (APQR) activities.
-Handle Quality Management System (QMS) activities, including Change Controls, Deviations, CAPA, and Investigations.
-Ensure compliance with cGMP, GDP, regulatory requirements, and company quality standards.
-Coordinate with Production, QC, Engineering, and other cross-functional teams to ensure product quality and compliance.
7. How to Apply:
Send your resume to 
sivasai.g@hetero.com

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