Virchow Biotech-Interview For Quality Assurance Department on 20 Feb 2024

Virchow Biotech-Interview For Quality Assurance Department on 20 Feb 2024

Virchow Biotech-Interview

Virchow Requirement of Manpower for QA (QMS,IPQA & validation)
We have an urgent requirement (VIRCHOW BIOTECH PVT LTD-U-4) for the following position with below mentioned details.
Designation: Jr Executive to Sr Executive
 
Department: Quality Assurance (QMS & IPQA)
No of Vacancies: 7 (QMS-2,IPQA-4 & Validation-1)
Qualification: M. Pharmacy, B. Pharmacy or M. Sc or B. Sc (Life Sciences)
Experience: 1 to 5 years
Budget- 1.6 to 4.2 lac.
Job Role: 
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 Q-Notification(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) Collect in-process and Finished sample as per Specifications and Protocol.
5) Supervision of RM/PM Sampling and dispensing procedure.
6) Planning, Execution and reporting of validation activities like equipment (Thermal & Non-Thermal) & Area.
7) Should aware of current guidelines for validation/QMS.

Interview Details: 
 
Venue: Virchow Biotech Pvt Ltd., Unit-4 Surveyno: 10/LU,10/LU2, Gaddapothara (V) Sangareddy (DT), Hyderabad Telangana-502319
Time: 9 am to 11 am
Walk-in’s on 20-02-2024
Job Category: pharma
Job Type: Full Time
Job Location: Hyderabad

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About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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