Posted:-1 days ago|
Platform:
Work from Office
Full Time
To be responsible for review of samples on HPLC, UV etc. as per specified in method of analysis.
1 To be responsible for all the investigations related to any incident, OOS, OOT and deviation related
to raw material and packing material.
2 To ensure and implementation of pharmaceutical quality system, cGMP, GLP and good
documentation practice in accordance with guidelines in QC.
3 Responsible for any other work allotted by the HOD/ Designee.
Morepen Laboratories
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.
Experience: Not specified
2.5 - 6.0 Lacs P.A.
Experience: Not specified
0.5 - 2.25 Lacs P.A.
Experience: Not specified
2.5 - 6.0 Lacs P.A.
kolkata, perundurai, raipur
13.0 - 20.0 Lacs P.A.
1.8 - 3.6 Lacs P.A.
greater noida
2.5 - 3.0 Lacs P.A.
0.5 - 0.5 Lacs P.A.
0.5 - 3.0 Lacs P.A.
4.2 - 6.0 Lacs P.A.
coimbatore
0.26 - 3.6 Lacs P.A.
