About Company:
TAGOOR LABS, a distinct pharmaceutical entity of TAGOOR GROUP, is a young and agile company that was established by the visionary leadership of Dr. P V Subramanyam Raju. The company, strategically conceived to cater to the backward‐integration requirements, steadily rose to global acclaim for delivering best‐in‐class APIs, Advanced Intermediates, and Key Starting Materials across the therapeutic areas. We are one of the fastest‐growing pharmaceutical companies in India and serve customers worldwide. Our state-of-the-art R&D and manufacturing facilities are spread across Telangana and Andhra Pradesh, India. With quality, safety, and environmental compliances at the center of what we do, we leverage our capabilities for customer value creation. Through our emphasis on supply assurance, product quality, and timely delivery, we are enabling our partners with cost leadership and accelerated launches. We at TAGOOR LABS have positioned ourselves to fully leverage the potential the industry has to offer in the near future.
Vacancy Details:
Job description:
Tagoor Laboratories Pvt Ltd
Hiring for DQA Department
Department: DQA
Experience: 2 to 10 Years
Qualification: Any Degree/Any PG
Openings: 2 Positions
Work Location: Jeedimetla – Hyderabad
Job Responsibilities:
1.Analytical method validation Review
2.Review technology transfer documents.
3.Process development reports and R&D process critical parameters.
4.Analytical method development reports.
5.Lab validation data Spec and MOA’s,
6.Structure confirmation Reports.
7.R&D and AR&D SOP’s Review.
8.Vendor Qualifications.
How to Apply?
Candidate must have experience in Pharma API
Interested candidates share your CV to: career@tagoor.com
Contact No: 9100990040
