Medical Device Process Development Tech II

Cirtec Medical; Enfield (CT); On-site; USD 44,000 - 48,000; Full time

Benefits offered by this job

Training and career development

Healthcare and well-being programs

Paid Time Off and 401(k) retirement

Competitive compensation plans

Job summary

Cirtec Medical in Enfield, CT is seeking a Process Development Technician II to support engineering and production under GMP and ISO standards. You will develop tools, write procedures, and help drive cost and quality improvements across medical device projects.

You will collaborate with cross functional teams, prepare engineering change orders, and ensure compliance with safety and regulatory requirements while applying DMAIC and Lean principles to reduce waste and improve processes.

Qualifications

• High school diploma or GED required.
• 3+ years in engineering/manufacturing for medical devices.
• Familiar with FDA, cGMP, ISO 9001/13485.
• Proficient with Microsoft Office software.
• Ability to read and interpret technical drawings and blueprints.
• Prior process development experience in a medical device environment.

Responsibilities

• Identify and promote Continuous Improvement objectives.
• Assist in defining Lean Manufacturing requirements.
• Develop processes and procedures to improve quality and cost.
• Originate and maintain written technical descriptions of processes and procedures.
• Represent engineering in Material Review Board discussions and cross functional teams.
• Maintain compliance to procedures and regulatory requirements.
• Follow safety policies, attend training, and wear PPE as required.
• Prepare project plans to satisfy timeline requirements.
• Prepare Engineering Change Orders for processes and components.
• Perform Corrective and Preventative Action tasks.

Skills

DMAIC

Process development

Blueprint reading

Microsoft Office

Cross-functional collaboration

Education

High school diploma or GED

Tools

Creo / Pro-E

SolidWorks

Job description

Cirtec Medical in Enfield, CT is seeking a Process Development Technician II to support engineering and production under GMP and ISO standards. You will develop tools, write procedures, and help drive cost and quality improvements across medical device projects.

You will collaborate with cross functional teams, prepare engineering change orders, and ensure compliance with safety and regulatory requirements while applying DMAIC and Lean principles to reduce waste and improve processes.