Stability Analyst - Quality Control

Description

Job Summary: A leading pharmaceutical company is seeking a Stability Analyst for its Quality Control department, responsible for analysis, equipment operation, and sample management. Key Highlights: 1. Key role in quality control and stability analysis 2. Operation of advanced analytical equipment such as HPLC/GC 3. Participation in OOS/OOT investigations and protocol development A prominent pharmaceutical company is currently seeking a Stability Analyst for its Quality Control department. **Requirements:** 1\. Degree holder and licensed in Pharmacy and Biochemistry, Chemistry, or Chemical Engineering. 2\. 2 to 3 years of experience in a pharmaceutical laboratory. 3\. Preferably 1 year of experience in stability studies or validations. **Technical Knowledge:** 1\. Proficiency in HPLC/GC. 2\. Dissolution and disintegration techniques. 3\. ICH guidelines (Q1A–Q1E). 4\. Pharmacopoeias: USP, BP, EP. **Responsibilities:** 1\. Perform assays for potency, impurities, dissolution, and other critical parameters. 2\. Operate analytical equipment (HPLC/GC). 3\. Monitor temperature and humidity in stability chambers (Zone IVb). 4\. Develop stability protocols and reports. 5\. Manage samples according to the Master Stability Plan. 6\. Participate in OOS/OOT investigations. **Benefits:** 1\. Competitive market-based salary 2\. Working hours from Monday to Friday 3\. Pleasant working environment Salary: S/.1\.00 \- S/.2\.00 per month Application Question(s): * What are your salary expectations? Work Location: On-site employment