Posted:22 hours ago|
Platform:
Work from Office
Full Time
Role & responsibilities 1. Quality Control Operations Supervise and perform analysis of in-process and finished pharmaceutical products as per pharmacopeial methods (IP, BP, USP, EP). Ensure timely sampling and testing of batches during manufacturing and post-production. Monitor compliance with Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP) . Conduct HPLC, GC, UV, IR, KF, Dissolution, and other instrumental testing . Maintain and calibrate laboratory equipment. 2. Documentation & Review Review and approve analytical reports, CoAs, and logbooks. Ensure proper documentation of results in LIMS or paper-based systems as per ALCOA+ principles. Investigate OOS, OOT, and deviations related to finished products and in-process samples. 3. Compliance & Regulatory Support regulatory inspections (USFDA, MHRA, WHO, etc.) and customer audits. Maintain readiness of QC labs as per regulatory requirements. Participate in internal and external audits and implement CAPAs. 4. Team Management & Training Supervise QC analysts and ensure task allocation and training. Develop SOPs, and provide on-the-job training to the QC team. Coordinate with QA, Production, and Warehouse teams for smooth QC operations.
Emil Pharmaceutical
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.
8.0 - 10.0 Lacs P.A.
10.0 - 14.0 Lacs P.A.
Experience: Not specified
3.0 - 6.0 Lacs P.A.
Hapur, Moradabad, Rajpura
Experience: Not specified
12.0 - 22.0 Lacs P.A.
5.0 - 9.0 Lacs P.A.
7.0 - 12.0 Lacs P.A.
Bengaluru
15.0 - 19.0 Lacs P.A.
7.0 - 11.0 Lacs P.A.
8.0 - 12.0 Lacs P.A.
Ahmedabad, Surat
3.25 - 7.0 Lacs P.A.
