Manufacturing Weekend Supervisor in San Jose, California at GCM MEDICAL AND OEM INC

SUMMARY

Responsible for day-to-day production activities in various manufacturing cells. Work with leads to ensure all scheduled jobs have the resources needed to meet customer deliver dates.

JOB RESPONSIBILITIES:

• Must be a team player as measured by his/her peers.
• Establish and maintain safe working environment.
• Develop and plan jobs by setting priority and assigning appropriate skill level to produce a quality product in spec and on time.
• Implement processes to improve ability to produce a quality product in spec and on time.
• Communicate and implement company policies, procedures, and objectives. Facilitate the flow of fact-based information.
• Provide technical assistance, guidance, and instructions as needed to all leads.
• Continuous improvement activity using the Define, Measure, Analyze, Improve & Control (DMAIC) methodology or Plan, Do, Check, Act (PDCA) cycle.
• Comprehensive knowledge of theoretical and practical aspects of blueprint reading, GD & T
• Recommend improvements in production methods, equipment, operating procedures, and working conditions.
• Establish maintenance requirements for equipment and facility in conjunction with Engineering and Maintenance personnel. Ensure timely maintenance is performed and proper records are maintained.
• Assess employee performance, provide frequent constructive feedback to employees, and conduct performance reviews. Implement corrective and disciplinary action as warranted.
• Identify and implement necessary personnel coaching, training, and development to upgrade and maintain employee skill levels to keep pace with current and future company requirements.
• Measure and manage productivity and the allocation of resources, including the control of overtime and hiring of personnel.
• Review CNC machine part programs, tooling aids, and machine set ups to ensure optimum output from resources, employee relations.
• Confer with supervisor and Programmers regarding drawings, sketches, and design data of a part to determine dimension and configuration of tool path(s)
• Coordinate production activities with other departments to optimize team members, schedules, and production.
• Maintain effective interface with other operations supervisors and other departments (i.e.; Planning, Engineering, Quality, Purchasing, Customer Service) to optimize production and process improvement activity.
• Work to continuously improve in all areas such as safety, quality, productivity, and cost reduction.
• ISO9001:2008 and ISO13485:2003 certification and compliance.
• Safety and OSHA compliance

REQUIRED

• High School Diploma or GED
• 10 to 15 years of progressive operational and management experience
• Relevant industry experience in the manufacturing of Medical Device and Semiconductor equipment
• Must be proficient in the Microsoft Office suite, Word, Excel, Power Point, Outlook
• Must have experience in the use of ERP system
• Proven track record in the management of manufacturing operations, engineering, and quality assurance
• Provide supervisory support above normal working hours and on weekends as needed.
• Good communication and interpersonal skills

DESIRED

• Associates or bachelor’s degree preferred
• Work experience in a fast -paced manufacturing environment
• Familiarity with Manufacturing Scheduling and Shop Control planning system such as Epicor is a plus
• Someone who proactively addresses concerns and potential issues prior to them negatively impacting business
• Someone who is personally committed to owning the outcome of identified results with a proven record of success and ownership when achieving goals
• A strong initiative with the ability to work independently or as part of a team
• A problem solver with a solution focused mindset