The ideal candidate will need to have the following qualities and experience:

• Degree or Diploma in Engineering or related discipline.
• Minimum 3 years supervisory experience working in a manufacturing environment preferably in medical device / biomedical / cleanroom working environment
• Ability to effectively interface with personnel from different departments on a technical level to accomplish the job goals and objectives.
• Good knowledge of Lean / Six Sigma
• Good written reporting skills.
• Strong communication and leadership skill

 

Our client, is actively searching for a Manufacturing Supervisor to join their team.

This role is a constructive step forward for anyone looking for excitement and challenges at work.

The responsibilities of this role encompasses:

• Supervises a group of assemblers and team leaders in a functional area so that the department objectives (schedules, performance, quality, etc.) are met.
• Responsible for work assignment, manpower planning, department leading, production cross training and employee relations.
• Responsible for the Daily WIP analysis and managing of daily rates.
• Responsible to interpret and monitor employees to ensure adherence to processes, policies, procedures and Department work rules related to quality, labor laws and safety.
• Verify and approve labor reports and maintain record of vacation hours of the employees in the work area.
• Conduct performance appraisals, discipline actions, and recommend salary increase in conjunction with Human Resources Manager as required.
• Assist Manufacturing/Industrial engineering in lean initiatives to maximize production flow, area layout, non-value added value added activities and special projects for productivity improvement.
• Perform material and WIP analysis of his/her area to minimize production disruption.
• Ensures compliance with company programs/procedures regarding ISO, GMP, and safety.
• Perform operations analysis and audits to assure a high level of productivity and efficiency in the areas to achieve Defect per Million (DPM), yield %, scrap and Total Product Cycle Time (TPCT) goals.
• Assure the best use of resources to obtain a high level of productivity and continuous follow up to established metrics to monitor employee performance, efficiency, utilization and equipment downtime.
• Assist the Engineering and QA teams for the Product Review Board (PRB).

 

The ideal candidate will need to have the following qualities and experience:

• Minimum 3 years supervisory experience working in a manufacturing environment preferably in medical device / biomedical / cleanroom working environment
• Ability to effectively interface with personnel from different departments on a technical level to accomplish the job goals and objectives.
• Good knowledge of Lean / Six Sigma
• Good written reporting skills.
• Strong communication and leadership skill