Quality Control Chemist - Pharma

Role Description The Quality Control Chemist – Pharma role is a full-time, on-site position based in Jaipur. The individual in this role will perform routine and non-routine testing of raw materials, intermediates, and finished pharmaceutical products using validated analytical methods. Daily responsibilities include operating and maintaining laboratory equipment, preparing reagents and standards, documenting test results in compliance with regulatory and internal quality requirements, and supporting investigations related to out-of-specification or atypical results. The Quality Control Chemist will collaborate with production, R&D, and quality assurance teams to ensure products meet predefined quality criteria and regulatory standards. The role also involves adherence to safety protocols, participation in internal audits, and contribution to continuous improvement of laboratory processes.

Qualifications

• Candidates should possess strong Quality Control skills, including knowledge of pharmaceutical quality standards, documentation practices, and GMP compliance.
• Candidates should possess hands-on Laboratory Skills such as sample preparation, wet chemistry techniques, handling of reagents, and adherence to laboratory safety procedures.
• Candidates should possess robust Analytical Skills, including data interpretation, troubleshooting test results, and working with validated analytical methods (e.g., chromatography, spectroscopy, titration).
• Candidates should possess proficiency with Laboratory Equipment, including operation, routine maintenance, and troubleshooting of instruments used in pharmaceutical testing.
• Candidates should possess Calibration skills, including performing and documenting instrument calibration and qualification in line with regulatory and internal requirements.
• Relevant qualifications include a bachelor’s or master’s degree in Chemistry, Pharmaceutical Sciences, or a related discipline, with prior experience in a pharma QC laboratory preferred.
• Additional beneficial skills include familiarity with regulatory guidelines (e.g., GMP, GLP), strong attention to detail, effective written and verbal communication, basic computer literacy for LIMS or electronic records, and the ability to work collaboratively in a structured, process-driven environment.