Officer (Quality Control)

Job Description of Q.C Officer A Quality Control (QC) Officer in the pharmaceutical industry ensures that products meet quality standards and regulatory requirements throughout the manufacturing process. Their responsibilities include analysing raw materials, in-process samples, and finished products, maintaining instruments, and ensuring adherence to cGMP and other relevant guidelines. They also document findings, investigate deviations, and support continuous improvement efforts. Key Responsibilities: · Sampling and Analysis: · Collecting and testing samples of raw materials, in-process materials, and finished products. · Performing various analytical techniques, including wet chemistry and instrumental analysis. · Analysing stability samples and preparing stability trend reports. · Status labelling of quality control Instruments, Chemical & Glassware. · Disposal of balance samples after completion of analysis and its documentation. · Instrument Maintenance and Calibration: · Maintaining and calibrating QC instruments, including HPLC, spectrophotometers, etc. · Documentation and Record Keeping: · Maintaining detailed records of analysis, including instrument logbooks, method validations, and SOPs. · Preparing and reviewing stability protocols and reports. · Preparation of certificates of analysis (COA) · Method Validation and Transfer: · Participating in method validation and transfer activities. · Deviation Reporting and CAPA: · Reporting and investigating deviations from established procedures and specifications. · Participating in the development and implementation of corrective and preventative actions (CAPAs). · Compliance and Auditing: · Ensuring compliance with cGMP, ICH, USFDA, ISO, and other relevant guidelines. · Providing documentation to auditors and assisting with audit activities. · Continuous Improvement: · Identifying areas for improvement in QC processes and procedures. · Supporting the implementation of new technologies and methods. Qualifications: · Bachelor's degree in chemistry, pharmacy, M.Sc. (Chemistry) or a related field. · Experience in pharmaceutical QC, preferably with a focus on analytical chemistry. · Knowledge of cGMP, ICH, USFDA, and other relevant guidelines. · Proficiency in various analytical techniques and instrumentation. · Strong analytical, problem-solving, and communication skills. Job Types: Full-time, Permanent Pay: ₹11,284.71 - ₹20,000.00 per month Benefits: Paid sick time Provident Fund Schedule: Rotational shift Supplemental Pay: Overtime pay Yearly bonus Work Location: In person Application Deadline: 15/05/2025 Expected Start Date: 01/06/2025