Virchow Biotech Pvt. Ltd is an ISO 13485:2015 and WHO – GMP certified leading global player in Bio – Pharma 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 strength.
Requirement of Manpower for Manufacturing (Vial, Cartridge, PFS & BFS)
- Designation : Trainee Executive to Sr Executive
- Qualification: B.Sc, M.Sc (All Streams) B.Pharm or M.Pharm, Diploma or B.Tech( Mech, ECE & Ele),
- Location : Hyderabad
- Experience : 0 to 6Years
- No Of Positions: 16
- Salary Range : 1.5 lpa to 5.4 lpa
Job Description:
- Should be able handle line activities of Manufacturing of Injectable.
- Should have basic idea on aseptic operations
- Should have an idea on CIP & SIP
- Control and adjust machine settings as needed to maintain desired line speed
- Responsible for accurate production and packaging changeovers as per packaging schedule
- Maintain a clean work area and clean equipment before and after shift.
- Perform basic troubleshooting and minor repairs to ensure production equipment runs efficiently.
- Remove damaged products or supplies, as needed.
Interested and Eligible candidates are requested to share the updated resume on the below mentioned mail-Id: [email protected] or [email protected]
- Date: 08 & 09.03.2024 (Friday & Saturday)
- Time: 9 am to 11 am
- Venue: Virchow Biotech Pvt. Ltd, Survey no. 172 part, Gagillapur, Quthbullapur, Hyderabad, Telangana-500043
We have an urgent requirement (VIRCHOW BIOTECH PVT LTD) for the fallowing position with below mentioned details.
- Designation: Trainee Executive or Executive
- Department: Quality Control
- No of Vacancies: 10
- Qualification: M.Pharmacy, B.Pharmacy or M.Sc or B.Sc (Life Sciences)
- Experience: 2 to 5 years
- Budget-2.4 to 4.2 lac
- 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
- Date: 08 & 09.03.2024 (Friday & Saturday)
- Time: 9 am to 11 am
- Venue: Virchow Biotech Pvt. Ltd, Survey no. 172 part, Gagillapur, Quthbullapur, Hyderabad, Telangana-500043
