To take responsibility of the shift in terms of management of staff, management of production
processes and quality targets
To ensure the smooth running of the production processes and maintain a positive work atmosphere
To take responsibility of the quality and product that is produced within the shift in line with company’s quality systems, processes and procedures
Coordinate daily production floor activities and delegate assignments to production personnel
Manage and motivate direct reporting employees by communicating job expectations, planning, monitoring and appraising job results; initiating, coordinating and enforcing systems, policies and procedures
Develop and maintain training programs to ensure that all personnel have the necessary skills to perform their duties safely and productively; and to ensure that training skills are met for current and future demands of the shift
Monitor and enforce working time, break, attendance, absence and leave planning of the production floor personnel
Conduct employee performance reviews and disciplinary actions; Assist in the selection and training of direct reporting employees
Monitor, measure and report on production related process performance and general issues
To ensure good communication of clear expectations to production personnel, develop personnel growth opportunities and monitor employee work performance
Maintain material and work flow throughout the manufacturing facility and ensure the workstations are supplied with material quickly and efficiently
Ensure equipment and tools are in good working order and available for use when required
To ensure that Health and Safety rules and regulations are adhered to during the shift and all matters relating to this are dealt with using the resources within the company
Bachelor’s Degree in Engineering, Manufacturing, Business Administration or equivalent.
Min 5 to 10 years of relevant working experiences in the medical device technology or pharmaceutical industry with minimum 3 years in managerial or supervisory capacity in a manufacturing environment.
Experience working in a clean room environment will be advantageous.
Good understanding of production and manufacturing processes and techniques.
Basic knowledge of Six Sigma will be advantageous.
Familiar with ISO13485 and GMP.
Proficient in SAP and MES.
Strong intercultural experience and excellent interpersonal skills
To apply, please visit to www.gmprecruit.com and search for Job Reference: 16132