Sr Technician Manufacturing

Cirtec Medical - Brooklyn Park, MN

Full-time - Entry Level

Brooklyn Park, MN

Miscellaneous Manufacturing

About the position

The Sr Technician Manufacturing position at Cirtec Medical is primarily responsible for operating laser systems and associated equipment in the manufacturing of complex medical devices. This role involves training lower-level operator assemblers, ensuring compliance with Good Manufacturing Practices (CGMP), and collaborating with engineering and manufacturing teams to resolve technical issues. The technician will also be involved in quality control, documentation, and process improvement initiatives.

Responsibilities

• Comply with all Good Manufacturing Practices (CGMP) requirements to ensure products are consistently produced and controlled according to the Quality System.
• Operate manufacturing workstations including all laser systems used in the manufacture of products.
• Set up and operate workstations, performing visual and dimensional inspections needed for manufacturing.
• Work with Engineering, customer representatives, and manufacturing personnel to resolve technical issues.
• Provide input/recommendations on tooling, equipment, processing sequence, programming requirements, and inspection techniques.
• Operate computerized motion controllers and modify/create motion control programs at an intermediate level.
• Follow operating manuals, maintenance instructions, Standard Operating Procedures, and work instructions accurately.
• Interpret technical drawings with an intermediate ability to understand nomenclature and dimensions.
• Document all work performed on inspection reports and travelers accurately.
• Perform in-process inspection of parts and/or assemblies according to specified requirements.
• Conduct various dimensional inspections using specific dies, gauges, verniers, and micrometers.
• Provide direction to lower-level operator assemblers within the manufacturing cell.
• Maintain professionalism in a high-pressure environment and adjust work hours as needed.
• Assist facilities department with equipment/room layouts and maintenance tasks.
• Recognize quality issues and communicate them to Quality and/or Supervisor.
• Assist with developing costs, processes, and documentation for new or modified products.
• Ensure the accuracy of Process Control Documents, Parameter Sheets, Work Instructions, and Standard Operating Procedures.
• Act as a resource during audits or customer visits for questions and demonstrations.
• Assist Engineers with parameter adjustments and process development, documenting activities accurately.
• Provide input to Engineering regarding tool design and troubleshooting processes.
• Perform duties with little or no supervision.

Requirements

• Must be able to read, write, and speak fluent English.
• High school diploma or General Education Degree (GED) is required.
• Associate degree or equivalent experience in the medical device industry.
• 3+ years of experience in a technical field.
• Meets requirements for a Sr. Operator Assembler.
• One year of applications experience or equivalent training.
• Moderate computer skills, including the MS Office suite.
• Ability to interpret technical drawings, blueprints, specifications, and illustrations.
• Strong analytical skills and ability to obtain secondary research information.
• Ability to learn and apply new technology.
• Ability to perform workstation setup for processing jobs using existing tooling and parameters.
• Ability to perform metallurgy (cross sections).
• Strong knowledge of ERP/MRP business functions.
• Understanding and implementation of Lean Manufacturing and Six Sigma for process improvement.
• Technical report preparation experience and good verbal communication skills.
• Ability to prioritize and manage multiple responsibilities.

Benefits

• Training and career development
• Healthcare and well-being programs including medical, dental, and vision
• Wellness and occupational health programs
• Paid Time Off
• 401(k) retirement savings with a company match