Quality Control Analyst / Chemist

Role & responsibilities

• Analyse raw materials, intermediates, in-process samples, finished APIs, and stability samples as per approved specifications and analytical methods.
• Operate and maintain HPLC, GC, UV-Visible spectrophotometer, FTIR, Karl Fischer apparatus, and other QC instruments, as applicable.
• Perform wet chemical analysis, titrations, assay, impurity profiling, and other routine laboratory tests.
• Prepare reagents, mobile phases, volumetric solutions, and reference standards.
• Maintain accurate analytical records, test reports, Certificates of Analysis (CoAs), and instrument logbooks.
• Ensure compliance with cGMP, GLP, GDP, SOPs, and ALCOA+ data integrity principles.
• Report and support investigations of OOS/OOT results, deviations, and laboratory incidents.
• Support method validation, verification, transfer, CAPA, audits, and regulatory inspections, as assigned.
• Ensure laboratory safety, proper chemical handling, sample traceability, and timely completion of testing.

Preferred candidate profile

• Qualification: M.Sc. Chemistry (Analytical/Organic),
• Experience: 3-5 years Quality Control in an API/pharmaceutical
• Technical Skills: Hands-on experience in HPLC, GC, wet chemical analysis, and other relevant analytical instruments.
• Quality Compliance: Working knowledge of cGMP, GLP, GDP, SOPs, , and data integrity practices.
• Key Competencies: Strong analytical ability, attention to detail, troubleshooting skills, documentation accuracy, integrity, and commitment to quality and safety.

Freshers M.Sc. Chemistry may be considered for trainee positions.