Quality Control Job at Sentiss | Pharmaceutical Sciences Graduates Apply Now for the Jr Executive Role
A leading pharmaceutical manufacturing plant (SNG) is inviting applications for the position of Jr Executive – Quality Control (QC). This Quality Control Job focuses on stability studies, raw material testing, and general QC responsibilities, ensuring compliance with ICH guidelines, cGMP, and pharmacopoeial standards. Candidates with 2–5 years of experience in QC jobs and strong analytical skills are encouraged to apply.
- Career Opportunity: Jr Executive – QC
- Job ID: 2667
- Location: Manufacturing Plant (SNG) – Quality Control (QC)
Key Responsibilities:
Stability Studies:
- Perform stability testing of drug products as per ICH guidelines (ICH Q1A, Q1B, etc.)
- Execute physical, chemical, and instrumental testing (HPLC, GC, UV, IR) on stability samples
- Maintain and monitor stability chambers (25°C/60% RH, 30°C/65% RH, 40°C/75% RH)
- Review and compile stability data and trend reports
- Ensure timely sampling, testing, and documentation for ongoing and new studies
- Assist in the investigation of OOS/OOT results in stability testing
Raw Material (RM) Testing:
- Conduct sampling and testing of raw materials (API, excipients) per pharmacopoeial standards (USP, EP, IP, BP)
- Perform identification, assay, and impurity profiling using analytical techniques
- Review raw material COAs and ensure vendor qualification compliance
- Maintain RM specifications and update per regulatory or pharmacopoeial changes
General QC Responsibilities:
- Operate and calibrate instruments like HPLC, GC, UV-Vis, FTIR, pH meter, balance, etc.
- Ensure all analytical work complies with cGMP, GLP, and SOPs
- Prepare and review analytical documentation (test reports, worksheets, protocols)
- Participate in internal and external audits (regulatory, client)
- Maintain accurate laboratory records, logbooks, and instrument usage logs
Qualifications:
- Education: B.Pharm / M.Pharm/ Pharmaceutical Sciences, or related field
- Experience: 2–5 years in a QC laboratory in the pharmaceutical industry, with experience in stability and RM testing
- Knowledge: Strong understanding of cGMP, ICH guidelines, and pharmacopoeial methods; proficiency in HPLC, GC, and wet chemistry; exposure to LIMS/ERP systems (preferred)
- Skills: Attention to detail, strong documentation, time management, teamwork, effective communication, and ability to work independently
