VBPL is an ISO 13485:2012 and WHO – GMP certified leading global player in Biopharma sector having more than 15 years of operational experience, situated at Hyderabad. We also have offices located in USA. Innovative, ever motivated Research team and uncompromising manufacturing team in providing quality products are our strengths.
Post : Executive
Quality Control Department
No of posts : 15
Qualification : M. Pharmacy, B. Pharmacy or M. Sc or BSc (Life Sciences)
Experience : 0 to 5 years
Budget : As per company norms
Preferably Males As per below mentioned
Job Description
1) Responsible for inspecting and/or testing products .
2) Should have worked on Aseptic (Injectable) products.
3) Responsible for testing & sampling finished products.
4) Should have basic communication.
5) Should be able to validate the collected sample .
6) Perform tasks as required GLP/ GMP according to allocation of QC manager and report monthly on their tasks.
7) To audit all laboratory worksheets, calibration protocols/reports and raw data archives to ensure the validity and accuracy of the data
8) To prepare and check Certificates of Analysis for all lots of raw materials and packaging materials tested in the QC Department
9) Checking the tidiness, orderliness and cleanliness of their working area
Quality Assurance (QMS & IPQA) Department
No of posts : 15
Qualification : M. Pharmacy, B. Pharmacy or M. Sc or BSc (Life Sciences)
Experience : 0 to 5 years
Budget : As per company norms
Preferably Males As per below mentioned
Job Description
1) Oversees the development, implementation, and maintenance of the Quality Management System within the Probiotics or Non-Aseptic manufacturing facility. This includes ensuring that all processes, procedures, and documentation comply with relevant regulatory standards such as Good Manufacturing Practices (GMP).
2) Manage change controls, deviations, and incidents by collaborating with stakeholders, ensuring proper closure upon execution.
3) Should take plant round for monitoring of entire production operations and confirm quality conformance to specifications.
4) Should check documents like equipment logbooks, temperature & humidity records .
5) Collect in-process and Finished sample as per Specifications and Protocol.
6) Supervision of RM/PM Sampling and dispensing procedure.
7) Machine Line clearance of Production Area
Walk in Interview
Date : 29th & 30th March 2024
Time : 9 am to 11 am
Venue : Virchow Biotech Pvt. Ltd, Survey no.172 Part, Gagillapur, Quthbullapur, Hyderabad, Telangana - 500043.
Interested candidates can share with the below mentioned mail-ld : raghu@virchowbiotech.com or hirings@virchowbiotech.com
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