Supervisor Production at Lorache Consulting Limited

Our client, a conglomerate with big investment in pharmaceutical sector require the service of a Supervisor Production. They invest in technologies and partner with others to create meaningful solutions and ultimately better results for the people they serve.

Position Title:    Supervisor Production
Location:    Ogun State
Reports to:    Production Head      

 KEY DUTIES AND RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO THE FOLLOWING ACTIVITIES:

• C-GMP to be followed in production manufacturing area. 
• Equipment setting, operation & preventive maintenance. Maintain equipment cleanness.
• Allocation of manpower at all works station. 
• To put all record and manufacturing area update & online documentation on daily basis
• Co-relation of daily production report of equipment’s, daily output analysis and performance on monthly basis. 
• To train Operators, and contract man power 
• Optimum utilization of equipment and control various breakdown, hazardous waste at manufacturing stage.
• Shift wise Volume Delivery in Mio at manufacturing stage.
• To update ERP entries, FG reports & monthly closure in ERP system, 
• To give BMR requisition to Q.A and completed BMR review before submission.
• To Co-ordinate with other department and handling of shift works in manufacturing department.
• To give dispensing plan to warehouse department. 
• Calibration of equipment/instrument as per the define frequency
• To maintain area cleanness and status labelling practices and all time audit readiness.
• All statutory compliances adhered to FDA, Internal, CQA, Regulatory, EHS, and Audits etc.
• Audit exposure – National Agency for Food and Drug Administration and Control (NAFDAC) & other regulatory agencies. Adhere to other compliance related to CQA, EHS and internal. 
• Exposure of IPQC instruments calibration & verification.
• Rejection monitoring and action plan, online rejection completion.
• Co-ordinate to engg for timely rectification of maintenance issues.
• Change parts and spare management.
• QMS activities- exposure of SOP writing, change control & deviation.
• RM/PM availability check from warehouse & to give dispensing plan to warehouse\\

REQUIREMENTS:

Qualification: Essential:  BPharm, MPharma
Experience:  5-7 years, 
Job Specific Skills: Computer Literacy, Aware with ERP system, Knowledge of regulatory guidelines, Problem Solving, Team work, People Management, 
Languages Known: English, Nigeria local language
Age (desirable):      Below 30-32 years