Description

• Ensure the cGMP Compliance and schedule M compliance in production. • Ensure the completion of production targets with zero quality issue. • Ensure the timely completion of investigation and implementation of corrective and preventive action. • Ensure the development progress periodically of personals and take necessary corrective action. • Ensure the compliance of inspection /Audit in coating area and revision of procedures/SOPs • To follow daily plan prepared based on the monthly/weekly plan. • To ensure the availability of core tablets, coating materials and equipment before plan. • To distribute the operational activities among the supervisors and operators of coating, capsule, printing and inspection to complete the daily targets. • To set & achieve the daily targets to achieve monthly targets. Trace the daily output of equipment with respect to the daily target and intimate the deviation with justification in OEE report. • To co-ordinate with cross functional departments (i.e. Dispensing, Granulation, Compression) for input material and co-ordinate with WIP, packing, QA, QC for sampling and release to packing. • To ensure the SAP transactions of completed products. • To ensure the cleanliness of area & equipment and to ensure the equipment parts,



change parts are place at designated location with proper status labelling. • Ensure the procedures are followed as per Standard operating procedure and continuous improvement in system/documents. • To verify the executed documents (BMRs) on daily basis and SOP formats on daily basis or Monthly basis based on the frequency of review. • To ensure all the SOPs are available at working place for ready reference. • To maintain the SOP records (i.e. Silicon tube, sieves, Audit trial review, consumable materials, etc.) for ready reference. • To maintain the records of equipment and instruments for calibration/verification and co-ordinate with cross functional team for timely calibration/verification where required. To ensure the calibration tags/verification tags available with equipment or instruments and to maintain the calibration, verification certificate for ready reference. • To provide the equipment are working as per design. • To verify the need of predictive maintenance and building maintenance and intimate to maintenance team through BDIS. • To ensure and tracking of the Users for each equipment/system for all supervisors and Operators in active status. • To ensure the no wastage of utilities when not required. • Any other job described by department/production/unit head.

📌 Executive (India)
🏢 Cadila Pharmaceuticals
📍 India