LVP Production Leader
at Fresenius Kabi
Port Elizabeth, Eastern Cape, South Africa -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 07 Nov, 2024 | Not Specified | 08 Aug, 2024 | 2 year(s) or above | Good communication skills | No | No |
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Description:
Fresenius Kabi is a global healthcare company more than 40,500 employees worldwide.
We are dedicated to a higher purpose “caring for life” which drives excellence in everything we do.
The manufacturing plant in Port Elizabeth produces both small and large volume parenterals.
The purpose of this position is to ensure that the production activity under his / her control is carried out in accordance with all relevant process procedures and production standards while fulfilling daily production targets.
§ To ensure Large Volume Parenteral Department meets its production requirements (ito of volume, quality, costs) effectively and efficiently at all times.
§ To assist with the Department Manager in production shift planning to commit LVP department to maximum attainment of that plan.
§ To ensure optimum labour utilization for the shift whilst organizing and controlling the day to day production requirements
§ To provide input to the department manager re annual department budget and monitor and control adherence in terms of days to day expense control.
§ To write, review and update the department’s Standard Operating Procedures and Good Manufacturing Practices.
§ Responsible for continuous improvement in the production area to ensure product and process efficiency and quality.
§ Provide support to line specific improvement projects.
§ Optimizing maximum efficiency of company resources with minimal reject and waste levels.
§ Control department staff discipline including settlement of disputes and grievances, absenteeism, Initiating, disciplinary action access control and timekeeping according to the Company Code of Conduct.
§ To commit the shift to comprehensive and on-going training and monitor training level of shift.
§ Provide timeous and accurate operational data as required for the monitoring of key indicators.
§ To take on ownership of shift KPIs.
§ To address non-compliances with BMR/logbook queries and drive RFT from an operations standpoint
§ Responsible for shift health and safety processes and conducting Safety Incident investigations.
§ Assume delegated responsibility of departmental manager during periods of absence or whilst on shift
§ Responsible for implementing continuous improvement initiatives and projects
§ Responsible for Logging and closure of incidents / Deviations / change controls on Kabitrack
§ Arriving 15 minutes prior to the shift commencing in order to perform floor walkabout and handover
§ From time to time carry out other jobs within the department / factory, which are consistent with the grade, qualification and training of the incumbent
- Appropriate tertiary qualification with a minimum National Diploma in either Technical, Pharmaceutical or Production Management fields.
- PMA qualification advantageous
- Minimum 3-5 years experience in Production environment with at least 2 years at supervisory level.
- Computer literate
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:2.0Max:5.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Clinical Pharmacy
Diploma
Management
Proficient
1
Port Elizabeth, Eastern Cape, South Africa