Team Member - Analytical Instrument Engineer

• UV-Visible Spectrophotometer
• FTIR Spectrophotometer
• Ensure proper use, cleaning, and upkeep of laboratory equipment as per approved SOPs.
• Perform instrument calibration, verification, and routine maintenance activities as per schedule.

• Maintain accurate and complete analytical records in compliance with cGMP, GLP, and ALCOA+ data integrity principles.
• Ensure proper documentation, logbook entries, laboratory registers, and traceability of all activities.
• Maintain compliance with SOPs, STPs, specifications, and applicable regulatory requirements.
• Perform SAP transactions related to sample tracking, result entry, and documentation management.

• Support investigations related to OOS (Out of Specification), OOT (Out of Trend), deviations, and laboratory incidents.
• Report discrepancies, abnormal observations, and incidents promptly to the Group Leader.
• Participate in CAPA implementation and effectiveness monitoring.

• Manage the handling and storage of chemicals, solvents, reference standards, and laboratory consumables.
• Prepare, standardize, and maintain volumetric solutions, reagents, and laboratory records.
• Prepare samples for external laboratory testing whenever required.
• Ensure timely destruction and disposal of retained samples as per approved procedures.
• Generate and print Certificates of Analysis (COA) as required.

• Adhere to laboratory safety requirements, JSA (Job Safety Analysis), and EHS guidelines.
• Ensure proper usage of Personal Protective Equipment (PPE).
• Maintain laboratory cleanliness, safety standards, and good housekeeping practices at all times.
• Follow all safety precautions during sample handling and analysis.

• Complete assigned training programs within the stipulated timelines.
• Support audits, inspections, and compliance initiatives.
• Undertake any additional responsibilities assigned by the Group Leader or Department Head.

• M.Sc. in Chemistry, Analytical Chemistry, Pharmaceutical Chemistry, or related discipline.

• 4–6 years of experience in Quality Control within the pharmaceutical industry, preferably in Oral Solid Dosage (OSD) manufacturing.
• Experience in handling analytical instruments and testing of Raw Materials and Packing Materials is essential.

• Strong knowledge of analytical testing techniques for Raw Materials and Packing Materials.
• Hands-on experience with HPLC, GC, KF, UV-Visible Spectrophotometer, FTIR, and Auto Titrator.
• Knowledge of cGMP, GLP, data integrity and regulatory compliance requirements.
• Familiarity with SAP/LIMS and laboratory documentation systems.
• Experience in calibration, verification, and maintenance of laboratory instruments.
• Understanding of OOS, OOT, deviations, CAPA, and investigation processes.
• Proficiency in preparation and standardization of reagents and volumetric solutions.

• Strong attention to detail and accuracy in analysis and documentation.
• Effective communication and interpersonal skills.
• Good problem-solving and troubleshooting abilities.
• Ability to work collaboratively in a cross-functional environment.
• High level of integrity, accountability, and compliance orientation.
• Proactive approach toward laboratory operations, safety, and continuous improvement.

Preferred Industry: Pharmaceutical Manufacturing – Oral Solid Dosage (Tablets, Capsules, Granules) Function: Quality Control (QC)