Shilpa Medicare Walk-ins For Quality Control (QC) & AQA – Formulations
- Education UG: Any Graduate, B.Pharma in Any Specialization PG: M.Pharma in Any Specialization, MS/M.Sc(Science) in Any Specialization
- 2 – 6 years
Role & responsibilities
for Analytical services- QC
*The candidate should have hands-on experience in executing analytical method validation and monitoring validation parameters in compliance with ICH and ANVISA guidelines. Proficiency in preparation and review of method validation protocols, raw data, and validation reports is required.
*Strong knowledge of formulation finished product analysis (both oral and injectable) in line with regulatory requirements. Hands-on experience in handling analytical instruments such as HPLC, GC (if LBPC refers to LC/GC, can clarify), FTIR, UV-Visible spectrophotometer, and water content determination techniques (e.g., Karl Fischer).
FOR AQA
Review and approval of analytical documents, raw data, audit trails, calibration/PM records, analyst qualification documents, and reference/working standard qualification records in compliance with GMP and data integrity requirements. Monitoring of LIMS data, chromatographic systems, and stability chamber performance to ensure accuracy, compliance, and quality standards.
Preferred candidate profile
Male candidate preferred
Time and Venue
23 May , 10.00 AM – 1.00 PM
Plot no 79, Road No 15, Survey No 125 IDA Mallpur, Nacharam, Uppal, Mandal, Telangana 500092
Contact – Karthik Kumar G
ABAC
