Analyst QC

You should possess a B. Pharmacy/M. Pharmacy (Pharmaceutical Analysis and Quality Assurance) or M. Sc. in Chemistry or equivalent with 5 to 8 years of experience in formulation pharmaceutical industries in the quality control department. In this role, you will be responsible for handling day-to-day activities related to sampling, testing, and release of active ingredients, inactive ingredients, packaging materials, in-process and finished products, stability samples. Your primary responsibilities include ensuring that all activities within the quality control section meet current applicable cGMP guidelines and regulatory expectations. You will be accountable for ensuring timely sampling, analysis, and release of materials used in product manufacturing. Additionally, you will oversee the qualifications and release of equipment, analyst qualifications, and relevant records maintenance. It is vital to implement and follow hygiene SOP within the QC and Microbiology areas and adhere to SOPs for equipment or instrument operation, cleaning, and maintenance. You must ensure compliance with cGMP, GLP, and Good Document Practices SOP within the QC. Your role involves preparation/review of protocols, quality systems implementation, and initiation/review of change controls, deviations, CAPA, OOS, and OOL reports. Participation in investigations, preparation and review of investigation reports, as well as review of method verification/validation and cleaning validation/verification protocols and reports, will be part of your responsibilities. Monitoring equipment/instrument qualification, process validation, and involving in qualification protocols related to QC equipment, utilities, instruments, or systems is essential. You will be responsible for ensuring all systems, facilities, utilities, equipment, and instruments within the QC are in a valid state daily. Additionally, ensuring preventive maintenance, calibration, planning and control of reference standards, columns, glassware, and other chemicals, investigating events/deviations, and maintaining reserve and regular samples are crucial duties. Moreover, you will be in charge of reviewing, revising, and maintaining QC SOPs, implementing CAPA for deviations/events/change controls/OOT/OOS, and preparation and approval of job descriptions of repartees. This role is located at Ferring India Laboratories.,