Section Head Manufacturing

Ready to help shape the future of healthcare? Your talent can bring our science to life

As a modern employer, we empower you to be yourself, share ideas and work collaboratively

Job purpose:

• Hold overall responsibility for the correct and efficient operation of the production line during all shifts.
• Meet set production targets with highest quality and highest practicable efficiencies
• Make decisions, allocate resources, and direct the activities of others to attain goals
• Lead the department to achieve high production plan, GMP and safety.
• Delivery of the needed pack in the right time with the right quality with the least cost per pack

In this role you will...

• Liaise with the Planners and Operations department to ensure efficient flow of materials.
• Conduct random inspections and Gemba's to monitor good manufacturing practice, health and safety, and housekeeping related standards needed for corrective actions required.
• Co-ordinate the training, assessments, and feedback for team members ensuring all personnel are competent to perform the tasks assigned to them.
• Engage and inspire staff by sharing the vision, area objectives, and helping staff to understand the value add of the work that they are responsible for
• Set expectations on individual's behavior and performance to ensure that regular feedback is provided through formal routes and in regular Gemba sessions.
• Set target conditions and deliver against these to achieve improvements in performance to meet future business needs.
• Deploy performance management process within area ensuring accurate and timely data is used and key metrics are achieved.
• Run safety, quality, and efficiency investigations using GSK problem solving to ensure completion of resultant actions.
• Ensure appropriate corrective action preventive actions, deviations, and problem-solving processes are used to avoid reoccurrence of issues.
• Carry out process confirmation to ensure adherence to standards and standard work by staff, and adherence to Leader Standard Work
• Actively participate and engage in Governance review meetings.
• Follow up and supervise all daily business activities & responsible for on job technical training of all sub-ordinates and their development, also member of technical training committee.
• Develop personal & procedures.
• The commitment to implement the SOPs instructions for the required work and to ensure that there is good training conducted.
• Adherence to standards of Data Integrity & ALCOA

Why you?

Qualifications & Skills:

• Bachelor's degree in sciences or related field
• Minimum of 5 years' experience in manufacturing within the Pharmaceutical industry: broad understanding of GMP regulations, EHS requirements, etc.

Preferred Qualifications & Skills:

• Demonstrated leadership skills
• Technical knowledge
• Elevated level of accuracy and attention to detail
• Ability to prioritize and manage multiple tasks effectively.
• Understanding of the relevant quality standards
• Good analytical skills and ability to think logically to solve problem.
• Ability to convey information clearly and accurately to groups/individuals verbally and in writing to ensure understanding.
• Strong interpersonal skills with the ability to listen and respond appropriately to others.

Informações de contato:
você pode se candidatar para esse cargo online selecionando o botão Candidatar-se agora.

Notificação importante para empresas/agências de emprego

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