Virchow- Interview For QA (QMS & IPQA) on 28 & 29th June 2024 

Virchow- Interview For QA (QMS & IPQA) on 28 & 29th June 2024 

Virchow- Interview

We have an urgent requirement (VIRCHOW BIOTECH PVT LTD-U-4) for the fallowing position with below mentioned details.
Designation: Jr Executive to Sr Executive
Department: Quality Assurance (QMS & IPQA)
No of Vacancies: 35 (QMS 15 IPQA 20)
Qualification: M. Pharmacy, B. Pharmacy or M. Sc or B. Sc (Life Sciences)
Experience: 2 to 6 years
Budget– 1.6 to 5.4 lac

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 reco 4
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.
 
Date : 28 & 29.06.2024 (Friday & Saturday)
Time: 9 am to 11 am
Venue: Virchow Biotech Pvt Ltd Survey no. 172 part, Gagillapur, Quthbullapur, Hyderabad Telangana – 500043
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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