Posted:2 months ago|
Platform:
Work from Office
Full Time
Job Responsibilities : Analysis of Vendor Approval samples. Preparation and Standardization of Solution, as and when required. Implementation of GLP / GMP requirements. Analysis of Raw Materials / Finished Products / Stability samples/Packing materials. Samples and related documentation as per cGMP requirement. Ensure analysis of Raw Materials / Finished Products / Stability Samples as per requirement from outside commercial lab. Review of laboratory chemicals. Calibration of instruments like HPLC, UV, IR, Dissolution, KF Potentiometer etc. as and when required. Performing Working standard qualification Preparation and Standardization of Solution, as and when required. Maintenance of Stability Incubators. .Loading removal of samples from Incubators its documentation. Review of Analytical data, calibration data, qualification data etc. Requirement: Minimum 1-3 years of experience in Quality Control Department Working in shifts Relocation to Plant location Qualification: B.Sc/ M.Sc/ B.Pharm
Pelltech Healthcare
Upload Resume
Drag or click to upload
Your data is secure with us, protected by advanced encryption.
4.0 - 6.0 Lacs P.A.
Vapi, Vadodara, Ankleshwar
2.0 - 7.0 Lacs P.A.
4.0 - 6.0 Lacs P.A.
Mumbai, Vasai
Experience: Not specified
1.0 - 3.0 Lacs P.A.
4.0 - 7.0 Lacs P.A.
Trivandrum
9.0 - 13.0 Lacs P.A.
Chennai, Pune, Delhi, Mumbai, Bengaluru, Hyderabad, Kolkata
7.0 - 9.0 Lacs P.A.
Experience: Not specified
2.0 - 3.25 Lacs P.A.
Bangalore Rural
1.0 - 3.0 Lacs P.A.
4.25 - 5.5 Lacs P.A.