Site Name : Pakistan - Sindh - Karachi Posted Date : Jun 8 2021 Job Purpose The purpose of this job is to supervise the manufacturing and filling operations of Lactam Sterile, so the products are delivered and supplied in full and on time to the patients at the end of our supply chain.
Educational Requirement Minimum Level of Education : Pharm-D Area of Specialisation : Industrial Pharmaceutics Experience Requirement 2-3 Years Key Responsibilities
Ensure strong compliance in Quality, EHS, Legal and other critical parts of the business related to the area responsibility.
Drive performance to improve quality and EHS standards in the area responsibility (Sterile Manufacturing), in accordance with GSK’s strategic objectives and with applicable law.
Drive a culture of transparency and total disclosure.
To make and agree daily / weekly / monthly production plan for Sterile.
To supervise manufacturing operations of sterile to achieve the production plan on time
Maximum utilization of resources for delivery of quality products and to improve KPIs.
Update respective production visual boards
Effectively implement GPS within the area of responsibility in manufacturing department
Embed OE culture within the area of responsibility in manufacturing department
Identify, develop and implement improvement / Operational Excellence (OE) projects to generate cost savings (Strategy Deployment).
Involve in investigations into incidents and ensure root cause is identified
Implement appropriate corrective and preventive actions are implemented
To Ensure SAP manufacturing data postings.
Provide training on new SOP’s to down the line staff
Maintain the training record of down the line staff
Ensure trainings are provided before the given deadline
Involve in origination of change controls
Attend change control meetings and provide valuable information as required
Have knowledge of Aseptic manufacturing and its guidelines.
Involve in right first time performance
Maintain the department in Inspection Ready’ state all the time.
Raise deviation as needed
Make certain 100% relevant SOPs are In-place In-use.
Conduct L1 inspection against approved schedule and record observations in the tracker.
Prepare and implement CAPA and monitor the timely closures of observations related to L1, L2, L3 & L4
Support the team in L2, L3 & L4 audits.
Ensure Data integrity compliance and improve the DI control (ALCOA principle) at Lactam Sterile Manufacturing.
Conducting Risk assessment & CRAs.
Ensure the embedding of living safety culture
Ensure EHS standards compliance by conducting EHS L1 audit; record observations, prepare CAPA and monitor timely closures.
Ensure LOTO application on respective machines.
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