Production Head | Indoco Remedies | Panaji, Goa

Job Description

• Maintain discipline, honesty, and dignity so as to maintain harmony and a good working atmosphere at the workplace. Respect all colleagues.
• Monitoring & Controlling Production activity on a daily/weekly/monthly basis including dispensing, manufacturing and packing.
• Ensure availability of necessary change parts, Tooling, replacement of damaged tools & updating affected documents, etc.
• Handling and Controlling necessary manpower required for the shift to meet daily production targets.
• Ensure that room conditions like temperature; Relative humidity, pressure differential, etc are monitored for all core and noncore areas.
• Ensure that all SOPs are followed
• Ensure that all production accessories, and equipment are properly maintained and cleaned and appropriate status labels are displayed
• Coordinate with other cross-functional departments like QA, QC, Engineering, and Warehouse Purchase for timely availability of material, equipment, documentation & analytical data.
• Ensure preventive maintenance is done as per predefined schedules.
• Ensure calibration status of all the equipment and instruments used in the production area.
• Ensure online completion of Batch and other in-process documents related to manufacturing and packing activity.
• Impart periodic training for the subordinates.
• Ensure that all safety precautions are followed during manufacturing and packing activity.
• Ensure qualification of new equipment is performed before its release for use.
• Ensure process, cleaning validations are performed as per VMP.
• To authorize the RM and PM dispensing work orders, BMRs, BPRs & Departmental SOPs
• Participation in management reviews of process performance, product quality, and quality management system and advocating the continual improvement
• To review and assess change controls, deviation & noncompliance’s; if any.
• To investigate deviations along with the QA head
• To investigate OOS/OOT for production-related discrepancies, if any.
• To review and investigate the market complaints.
• To ensure implementation of data integrity principles.
• To review the departmental equipment/ Instruments qualification/ requalification documents.
• To review user requirement specification documents & the departmental equipment.
• To review risk assessment Protocol documents.
• To authorize the documents in absence of the site Head.
• To manage employees working in the department and understand skills and plan improvement in individual functions.
• To understand the importance of data integrity & its principles & ensure that the same is strictly followed.
• To ensure that all personnel works proactively to achieve the required goods.
• To execute planned product at the site as per laid down requirements in batch records.
• To develop review skills about department functions.
• To ensure that the handling of solvent is done properly.
• Co-Ordination with Packaging and Purchase for development of packing materials.

Qualification: B.Pharma, M.Pharma