About Company:
Virchow Biotech (P) Ltd is an ISO 13485:2012 and WHO-GMP certified leading global player in Biopharma sector having around 20 years of operational experience and is situated at Hyderabad, India. We also have offices located in USA. Throughout the years, the company has been successful in Research and development, clinical trials, large-scale production and Commercialization of Plasma Products, Recombinants, Biologicals and Bio-Pharmaceuticals. With 1160 employees on the board, VBPL has an expansive infrastructure, which comprises of WHO cGMP and USFDA certified state-of-art clean-room manufacturing facilities and excellent fill-finish lines for PFS, vials, cartridges and lyophilized drug products. VBPL focuses on the manufacturing of a wide range of biologicals and bio-generics by genetic engineering, classical fermentation or extraction technologies. Apart from this, we also offer Contract Research and Manufacturing services, co-development of products for various markets and customers around the world. Virchow Biotech is the part of Virchow Group incorporated in 1981. Other group companies are leading manufacturers of Sulphamethoxazole, Ranitidine, Cephalosporins and various other APIs. VBPL’s achievements include being the first company in the world to commercialize biogenerics of PDGF, Teriparatide, Pegylated Interferon and Rasburicase. VBPL has a wide product portfolio across Wound care, Gynaecology, Urology, Oncology, Vaccines and Probiotics etc. Our mission is to provide high quality Biopharma products at an affordable price. Serving economically challenged patients across the globe through Biotechnology by extending our product base across various therapeutic segments.
Website
http://virchowbiotech.com
Vacancy Details:
We have a walk-in on 15 .03.2025 for Executive or Sr. Executive (QA-IPQA-Injectable or Biologics) for VIRCHOW BIOTECH PVT LTD, Hyderabad.
Department: QA-IPQA-Injectable or Biologics (DS & DP)
Designation: Executive or Sr Executive
No of Vacancies: 10
Qualification: B. Pharma, M. Pharma or M. Sc (All streams)
Experience: 2 to 5 Years
Budget: Based on their core competency and present CTC
JOB DESCRIPTION:
Responsibilities:
1) perform IPQA activities at shop floor in each stage of sterile manufacturing and packing.
2)QA overview for clean room behaviour and aseptic activity.
3)Review of batch processing records.
4)Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release.
5)Review of documents of respective areas and logbooks for adequacy and completeness.
6)QA overview for receipt of material from warehouse to production.
7) IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities.
8)Review and Control of SOPs, Specification, BPR issuance, Master Formulae and Records.
9)Preparation & Review of process validation protocols and reports.
10)Executing the validation/revalidation activity in the absence of authorized person.
11)Any job activity assigned by HOD
12) Responsible for regulatory audits with exposure
Note: Preference will be given to immediate joiners.