5 - 10 years
5 - 7 Lacs
Posted:2 days ago|
Platform:
Work from Office
Full Time
Analysis of samples as per existing release spe c ifi c ations and testing methods Ensuring strict adherence to Current Good Manufacturing Practice (cGMP) and Current Good Laboratory Practice (cGLP) to maintain high product quality Executing thorough investigation of Out of Specification (OOS), Out of Trend (OOT), and incidents, ensuring the implementation of appropriate Corrective and Preventive Actions (CAPA) when required. Playing a crucial role in Stability Management within Quality Control, including monitoring all stability-related activities and chambers. instrument HANDLED AUDIT FACED USFDA, EUGMP PLEASE SHARE YOUR UPDATED CV ON placement@balpharma.com Thanks, Kamal
Bal Pharma
Upload Resume
Drag or click to upload
Your data is secure with us, protected by advanced encryption.
Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.
We have sent an OTP to your contact. Please enter it below to verify.
Instantly access job listings, apply easily, and track applications.
5.0 - 7.5 Lacs P.A.
6.0 - 7.0 Lacs P.A.
2.5 - 4.0 Lacs P.A.
Bengaluru
4.0 - 5.0 Lacs P.A.
7.0 - 11.0 Lacs P.A.
5.0 - 10.0 Lacs P.A.
Pune
15.0 - 22.5 Lacs P.A.
Faridabad
3.0 - 3.5 Lacs P.A.
Bengaluru
Experience: Not specified
2.4 - 3.0 Lacs P.A.
Sri City, Chennai
6.0 - 10.0 Lacs P.A.
