Cretex Medical is a leading contract manufacturer of precision components and assemblies for the medical device industry. Our customers view us as a trusted partner in the areas of injection molding, laser processing, metal stamping and device assembly. Learn more at www.cretexmedical.com.
Supervisor I Position Summary:
The Supervisor I will be responsible for directing and coordinating manufacturing processes and staff to ensure production objectives are achieved at the lowest cost consistent with customer delivery and quality requirements. This role drives continuous improvement to the methods of manufacturing and ensures a safe and procedural compliant work environment.
Shift Available: 2nd Shift
Responsibilities
Supervisor I Responsibilities:
Maintain workflow by monitoring steps of the process; setting processing variables; observing control points and equipment; monitoring personnel and resources; studying methods; implementing cost reductions; developing reporting procedures and systems; facilitating corrections to malfunctions within process control points; initiating and fostering a spirit of cooperation within and between departments
Ensure the production schedule is attained and issues are resolved in a timely manner
Maintain quality and safety by establishing and enforcing standards
Communicate and deliver employee communication tools for job performance to include annual performance goals, employee recognition, training, and development, coaching and counseling
Lead staff through visual metrics and tiered accountability meetings
Monitor staffing levels and partners with Human Resources on talent management initiatives
Enforce company standards by following and enforcing policies and procedures
Lead project management activities and teams
Complete special projects as needed
Drive process improvements in quality, delivery, inventory, and safety procedures
Ensure work instructions, set up sheets, and checklists are used and understood
Enter production information into the ERP system on a timely basis
Support and comply with the company Quality System, ISO, and medical device requirements
Read, understand, and follow work instructions and standard work
Partner with other business segments: sales/marketing, customer service, engineering, quality, and finance
Understand customer needs and the core business markets we serve
Ensure business systems are implemented, maintained, and functioning properly
Participate in required company meetings
Maintain an organized work area (5S)
Participate in the Operational Excellence Program
Complete all other work duties as assigned
Ability to work in a manufacturing environment
Qualifications
Supervisor I Requirements:
3 years of experience leading processes and teams in a manufacturing environment
Lean Practitioner Certification
Ability to consistently achieve short and long-term business results
Microsoft Office proficiency (Outlook, Word, Excel, PowerPoint, Publisher)
Clear and effective verbal and written communication skills
Attention to detail
Organizational skills
Ability to work in a fast-paced team environment
Ability to prioritize and multitask
Preferred Knowledge, Skills, and Abilities:
Associate Degree in a Business or Technical field
Supervisory Certificates
Functional experience
Quality and/or Operational Excellence training such as Lean, Six-Sigma, ASQ-CQE, etc.
Working knowledge of ISO 9001/13485
Mechanical Aptitude
Continuing Education; including participation in local chapters, associations, and/or organizations
