Virchow Group comprises of six independent active pharmaceutical ingredient (API), one
bio-pharmaceutical and two drug intermediate companies. All these companies function
independently with their own management structures.
Incorporated in 1981, the flagship company of the group, Virchow Laboratories Limited is
today the largest producer of Sulfamethoxazole in the world. In fact, Virchow Group services
more than 80% of the worldwide Sulfamethoxazole requirement. Other group companies are
world leading manufacturers of Cephalosporin’s, Tramadol and various other
APIs and bio-pharmaceutical Finished Dosage Forms (FDF’s). Virchow also undertakes
custom synthesis and manufacture of drug intermediates and bulk chemical
DATE AND TIME:
- Date: 13 &14.12.2024 (Friday & Saturday )
- 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-Id: raghu@virchowbiotech.com, hirings@virchowbiotech.com
POSITIONS:
- Designation: Jr Executive to Sr Executive
- Department: Quality Assurance (QMS, IPQA, VALIDATION)
- No of Vacancies: 60 (QMS 5, IPQA 30, VALIDATION-15)
- Qualification: M. Pharmacy, B. Pharmacy or M. Sc or B. Sc (Life Sciences)
- Experience: 2 to 8 years
- Budget- based on their present ctc.
Job Description:
- 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).
- Manage change controls, deviations, and incidents by collaborating with stakeholders, ensuring proper closure upon execution.
- Should take plant round for monitoring of entire production operations and confirm quality conformance to specifications.
- Should check documents like equipment logbooks, temperature & humidity records .
- Collect in-process and Finished sample as per Specifications and Protocol.
- Supervision of RM/PM Sampling and dispensing procedure.
- Machine Line clearance of Production Area.
Documents :
- Latest Resume
- Latest increment letter & recent 3 payslips
- Relieving & service certificates from previous employers
- Educational documents
- Aadhaar & PAN copies
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