Job Posting: Walk-In Interview at Virchow Biotech for Various Positions
Company: Virchow Biotech Pvt. Ltd.
Location: Hyderabad, Telangana
Sector: Bio-Pharma
Certifications: ISO 13485:2015, WHO-GMP
Event: Walk-In Interview for ITI, Diploma, B.Sc, M.Sc, B.Pharm, M.Pharm Freshers and Experienced
Interview Dates: 28th & 29th June 2024 (Friday & Saturday)
Interview Time: 9:30 AM – 11:00 AM
Venue: Virchow Biotech Pvt. Ltd, Survey No. 172 part, Gagillapur, Quthbullapur, Hyderabad, Telangana – 500043
Send CV To: raghu@virchowbiotech.com or hirings@virchowbiotech.com
Job Openings:
We are hiring for various positions across different departments. Join us for this exciting opportunity to advance your career in the Bio-Pharma sector.
Positions Available:
- R&D
- Junior Research Associate: 1-4 years experience, M.Sc (O.C, A.C), B.Pharm, M.Pharm, 5 vacancies, ₹2.4 LPA – ₹3.6 LPA
- Research Associate: 1-4 years experience, M.Sc (O.C, A.C), B.Pharm, M.Pharm
- Quality Assurance
- Jr Executive to Sr Executive: 2-6 years experience, M.Pharm, B.Pharm, M.Sc, B.Sc (Life Sciences), 35 vacancies (QMS 15, IPQA 20), ₹1.6 LPA – ₹5.4 LPA
- Quality Control
- Jr Executive or Sr Executive: 2-5 years experience, M.Pharm, B.Pharm, M.Sc, B.Sc (Life Sciences), 10 vacancies, ₹2.6 LPA – ₹4.8 LPA
- Manufacturing
- Trainee Executive to Sr Executive: 0-6 years experience, B.Sc, M.Sc (All Streams), B.Pharm, M.Pharm, ITI, Diploma, B.Tech (Mech, ECE, Ele), 50 vacancies, ₹1.7 LPA – ₹5.4 LPA
Job Descriptions:
R&D Department:
- Handle all analytical research work, including method development for analyzing in-process samples using HPLC and GC.
- Support regulatory affairs with analytical method validation.
- Identify and characterize unknown impurities using various analytical tools.
Quality Assurance (QMS & IPQA):
- Oversee the development, implementation, and maintenance of the Quality Management System.
- Manage change controls, deviations, and incidents.
- Monitor entire production operations to ensure quality conformance.
Quality Control:
- Inspect and test products, especially aseptic (injectable) products.
- Perform GLP/GMP tasks and audit laboratory worksheets.
- Prepare and check Certificates of Analysis.
Manufacturing:
- Handle line activities of manufacturing injectables.
- Understand aseptic operations, CIP & SIP.
- Control machine settings and perform basic troubleshooting.
Join us for this exciting opportunity to advance your career in the Bio-Pharma sector. We look forward to meeting you!
For more information:
