Job Title: QC Analyst – HPLC Specialist Location: Dabaspet , Bangalore – 562111, India Department: Quality Control Industry: Pharmaceuticals (Formulations) Experience: 2–5 years Employment Type: Full-time Company Overview: We are a reputed pharmaceutical formulation company based out of Bangalore committed to delivering high-quality products to domestic and export markets. We are currently seeking a skilled and detail-oriented QC Analyst with hands-on experience in HPLC to join our Quality Control team. Position Summary: The QC Analyst will be responsible for conducting analytical testing of raw materials, in-process samples, and finished products with a primary focus on HPLC. The ideal candidate should be well-versed in regulatory standards and capable of working in a fast-paced, cGMP-compliant laboratory environment. Key Responsibilities: Perform routine and non-routine analysis using HPLC for assay, dissolution, related substances, and stability studies Preparation, review, and maintenance of test data, analytical records, and reports in compliance with GMP and GLP Calibrate, operate, and troubleshoot HPLC and other analytical instruments (e.g., UV, FTIR, pH meter) Conduct testing of raw materials, intermediates, and finished formulations as per pharmacopeial and internal specifications Assist in method validation and transfer activities Investigate and document OOS/OOT results and deviations Ensure compliance with quality standards, SOPs, and regulatory requirements Maintain proper documentation and data integrity in line with audit expectations Qualifications and Skills: B.Pharm / M.Pharm / M.Sc (Analytical Chemistry / Pharmaceutical Chemistry preferred) 2–5 years of experience in a pharmaceutical QC lab Strong hands-on experience in HPLC method execution and troubleshooting Familiarity with regulatory guidelines (e.g., ICH, cGMP, WHO, USFDA) Working knowledge of LabSolutions/Chromeleon / Empower or similar HPLC software Good documentation skills and attention to detail Ability to work independently as well as part of a team
Job Title: QA Executive – Oral Solid Dosage (OSD) Location: Dabaspet , Bangalore - 562111 Department: Quality Assurance Industry: Pharmaceuticals Experience: 2–5 years (OSD QA experience mandatory) Employment Type: Full-time About the Company: We are a leading pharmaceutical manufacturer based out of Bangalore committed to delivering high-quality oral solid dosage formulations. Our facility is WHO GMP-compliant and serves both domestic and regulated international markets. We are currently looking for a dedicated QA Executive to strengthen our Quality Assurance team. Role Overview: The QA Executive will play a critical role in ensuring product quality and regulatory compliance across all stages of manufacturing. The candidate will be actively involved in quality systems, in-process controls, documentation review, and regulatory readiness. Key Responsibilities: Review and approval of Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) Execution and review of process validation, cleaning validation, and hold time studies Line clearance, in-process checks, and compliance monitoring on the shop floor Handling deviations, CAPA, change controls, and quality risk management Coordination for internal audits, regulatory inspections, and customer audits Oversight of document control and SOP implementation Ensuring adherence to cGMP, GDP, and data integrity practices Supporting cross-functional teams including production, QC, and RA Required Qualifications & Skills: B.Pharm / M.Pharm / M.Sc (Chemistry or related discipline) 2 to 5 years of relevant experience in QA within an pharmaceutical manufacturing setup Sound understanding of regulatory guidelines (USFDA, EU-GMP, WHO-GMP, etc.) Strong documentation and communication skills Proficient in handling QMS activities and audit preparedness Familiarity with electronic systems like TrackWise, LIMS is an advantage