Maithri Drugs is one of India’s fast-growing pharmaceutical companies. Maithri’s strategic focus is on active pharma ingredients (APIs). The company is widely recognized for its excellent research & development and aggressive growth strategies. Our 35 US DMFs and 10 CEPs in a short span attest to our R&D excellence. Maithri’s manufacturing facility is located in Hyderabad. This facility is audited and approved by the US FDA. In addition, our facility is certified according to the standards of DCGI, WHO GMP, and ISO 9001:2015 We have a portfolio of 65 products and are continually expanding. Our products cover a broad range of therapeutic categories including CNS, anti-anaemics, anti-bacterial, anti-diabetic, anti-fungal, anti-hyperthyroidism, anti-inflammatory, anti-viral, antihypertensive, cardiovascular, etc
Vacancy Details
JOB SPECIFICATIONS:
1. Handling of Change Control, OOS, Market Complaints, Deviations and its CAPA, Return Goods and Recalls.
2. Preparation and review of QA SOP’S
3. knowledge in handling vendor qualification activities. Should be able to handle/support in customer & regulatory audits.
4. Preparation and verification of annual product quality review (APQR’s)
5. Perform the risk Assessment.
Date: 13th Aug’ 2022
Time: 09:00 AM to 01:00 PM
Interview Venue and Work Location: Maithri Drugs Private Limited, Bonthapally, Sangareddy District, Telangana- 502313. Landmark: Lane Beside Bharat Petroleum Bunk, Bonthapally.
Contact: 040 69076672/08455 69410
The app functions as a digital ledger that replaces manual registers for small community groups,…
Now, anyone can make their own Household Mapping , a service that is useful for automatically…
If you want to complete your ration card eKYC through the Mera eKYC App but are experiencing issues like downloading,…
The CSC is a strategic cornerstone of the National e-Governance Plan (NeGP), approved by the…
As a data services company clickworker uses its own trusted platform to set up your data…
To submit your Enumeration Form online (e.g., during the Special Intensive Revision - SIR process),…